XIAO2008 Revis+úo

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International Journal for Parasitology xxx (2008) xxxxxx www.elsevier.com/locate/ijpara
Molecular characterisation of species and genotypes of Cryptosporidium and Giardia and assessment of zoonotic transmission
Lihua Xiao a, Ronald Fayer b,*
a
Division of Parasitic Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA b USA Department of Agriculture, Agricultural Research Service, Beltsville, MD 20705, USA Received 9 January 2008; received in revised form 25 March 2008; accepted 25 March 2008
Abstract The molecular characterisation of species and genotypes of Cryptosporidium and Giardia is essential for accurately identifying organisms and assessing zoonotic transmission. Results of recent molecular epidemiological studies strongly suggest that zoonotic transmission plays an important role in cryptosporidiosis epidemiology. In such cases the most prevalent zoonotic species is Cryptosporidium parvum. Genotyping and subtyping data suggest that zoonotic transmission is not as prevalent in the epidemiology of giardiasis. Molecular characterisation of Cryptosporidium and Giardia is a relatively recent application that is evolving as new genes are found that increase the accuracy of identication while discovering a greater diversity of species and yet unnamed taxa within these two important genera. As molecular data accumulate, our understanding of the role of zoonotic transmission in epidemiology and clinical manifestations is becoming clearer. Published by Elsevier Ltd on behalf of Australian Society for Parasitology Inc.
Keywords: Giardia; Cryptosporidium; Zoonoses; Epidemiology; Molecular; Genotyping; Subtyping
1. Introduction Within the genera Cryptosporidium and Giardia are multiple species and genotypes that infect humans, domesticated livestock, companion animals and wildlife worldwide. These species and genotypes exhibit a wide range of biological diversity, each diering in their ability to infect one or multiple host species and each varying in prevalence of infection between and within countries. Hosts of all ages are aected, but generally the young are infected more frequently than adults. Age-specic preferences for some species of Cryptosporidium have been observed in animals. Clinical signs vary depending on the age and health of the infected host and the genetic background, condition and infective dose of the parasite. Much
Corresponding author. Tel.: +1 301 504 8750; fax: +1 301 504 6608. E-mail addresses: ronald.fayer@usda.ars.gov, rfayer@anri.barc.usda. gov (R. Fayer).
*
of the scientic literature describing host range, prevalence and clinical signs has identied Cryptosporidium oocysts and Giardia cysts based on microscopic observations that rely on very limited morphological dierences. To protect public health and animal well-being, recent eorts have focused on more precisely identifying each organism associated with infections in humans and animals based on genes found in those organisms. As genetic data are accumulating in scientic literature and digital media, we are greatly improving our understanding of the complex relationship between humans and animals as hosts and reservoirs for these parasites. Cryptosporidium, an apicomplexan protist, is reported to infect persons in 106 countries (Fayer, 2008). Giardia, a binucleate, agellated, facultative anaerobic protist, similarly widespread, is the most common intestinal parasite of persons in developed countries and approximately 200 million people in Asia, Africa and Latin America have symptomatic infections with about 50,000 cases reported
0020-7519/$34.00 Published by Elsevier Ltd on behalf of Australian Society for Parasitology Inc. doi:10.1016/j.ijpara.2008.03.006
Please cite this article in press as: Xiao, L., Fayer, R., Molecular characterisation of species and genotypes ..., Int. J. Parasitol. (2008), doi:10.1016/j.ijpara.2008.03.006
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2 L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx
each year (Yason and Rivera, 2007). Estimates of prevalence for both of these parasites vary greatly because reporting is not universally required, diagnostic methods vary greatly, and many persons have no access to medical care or do not seek it. For cryptosporidiosis, in the USA 3,505 cases were reported in 2003, 3,911 in 2004 and 8,269 in 2005 (Yoder and Beach, 2007). The large increase in reporting in 2005 was primarily attributed to a single recreational water-associated outbreak. For giardiasis in the USA, voluntary reporting to the Centers for Disease Control and Prevention (CDC) surveillance systems from 1998 through 2003 indicated that the total number of cases varied between 24,226 and 20,075 annually (Hlavsa et al., 2005; Yoder and Beach, 2007). The greatest number of cases of both cryptosporidiosis and giardiasis was reported for children 19 years of age and for adults 3039 years of age (Hlavsa et al., 2005; Yoder and Beach, 2007). Also, for both parasites a seasonal peak in age-related cases coincided with the summer recreational water season, possibly reecting increased use of rivers, lakes, swimming pools and water parks (Hlavsa et al., 2005; Yoder and Beach, 2007). 2. Life cycles Cryptosporidium completes its life cycle in a single host with stages similar to those of the coccidian genera Eimeria and Isospora. Oocysts containing four infectious sporozoites are excreted in faeces. Oocysts of some species such as Cryptosporidium parvum can remain infectious in cool, wet conditions for 6 months or longer (Fayer, 2008). After oocysts are ingested in contaminated water or food, from fomites, or from direct contact with infected persons or animals, sporozoites are released in the small intestine and invade epithelial cells. All subsequent endogenous stages are intracellular but extracytoplasmic, appearing to rest on the surface of villar epithelial cells. Two asexual cycles each produce four to eight merozoites. Second stage merozoites develop into male or female sexual stages and fertilisation results in oocyst formation. Some oocysts might auto-infect but most, if not all, oocysts are excreted in faeces. A report of the in vitro cultivation of Cryptosporidium andersoni through its entire life cycle included the description of a previously unrecognised extracellular stage (Hijjawi et al., 2002). This stage, also isolated from faeces of cattle, appeared to undergo syzygy, and the ssrRNA gene from this stage conrmed it to be C. andersoni (Hijjawi et al., 2002). Similar extracellular stages, observed in in vitro cultures infected with C. parvum from cattle and from mice, led to the conclusion that these novel life cycle stages conrmed the relationship of Cryptosporidium to gregarines (Hijjawi et al., 2002). Hijjawi et al. (2004) later reported continuous development of C. parvum in cell-free medium through all life cycle stages. Attempts to obtain the developmental stages reported by Hijjawi et al. (2004) using a similar serum-free culture system were unsuccessful (Girouard et al., 2006). However, Rosales et al. (2005)
reported nding similar stages in cell cultures. More recently, Woods and Upton (2007) indicated that several of the photomicrographs of developmental stages appeared to be budding yeasts (as in Hijjawi et al., 2004, Figs. 1ac and 2d; Rosales et al., 2005, Fig. 1), host cells or other contaminating debris (as in Hijjawi et al., 2004, Figs. 2ac, 3aj and 4a, b, d), and fungal conidia (as in Hijjawi et al., 2004, Fig. 4c). Therefore, until an independent laboratory conrms that Cryptosporidium can develop extracellularly and that the forms reported as gregarine-like stages are truly stages of Cryptosporidium, members of this genus should still be considered obligate intracellular parasites. Giardia has a simple and direct life cycle. Cysts excreted in faeces contain a mitotically arrested trophozoite that can remain infectious for months in a wet, cool environment. After cysts are ingested, trophozoites emerge in the duodenum and complete mitotic division. Infection in new hosts is established by ingestion of cysts and repeated divisions of trophozoites that attach to the surface of the intestinal microvilli beneath the mucus layer via a ventral adhesive disc. Cysts form in response to intestinal conditions such as the presence of major bile salts. They pass through the intestine in the faeces and are spread by contaminated water and food, and by physical contact. 3. Taxonomy and nomenclature Cryptosporidium and Giardia are genera, each consisting of multiple species. The taxonomy of currently recognised species of both genera is summarised in Tables 1 and 2. Assemblages of Giardia and genotypes of Cryptosporidium have no taxonomic status but are helpful in identifying genetically unique organisms for which limited biological information is available. Some genotypes have been named as species when sucient information regarding their morphology, biology and genetics became available. The genus Cryptosporidium consists of 18 species (Table 1) and over 40 genotypes (Xiao and Ryan, 2008). As biological and molecular data increase, many of the genotypes are expected to be named as valid species. More than 150 mammalian hosts were reported to be infected with C. parvum, a C. parvum-like parasite or simply Cryptosporidium (Fayer, 2008) based on microscopic observations of oocysts in faecal specimens. Most will have to be re-examined using molecular methods to validate the species or determine the genotype. Although oocysts of Cryptosporidium from animals in one class of vertebrates generally have not been infectious for those in another class, there are exceptions. Cryptosporidium meleagridis, rst reported to infect turkeys, has been detected in faeces from immunocompromised and healthy humans (Pedraza-Diaz et al., 2000; Guyot et al., 2001; Xiao et al., 2001; Gatei et al., 2003) and has been transmitted from an infected patient with diarrhoea to chickens, mice, piglets and calves (Akiyoshi et al., 2003). Cryptosporidium muris and C. andersoni, originally recognised as parasites of the stomach of mammals, have been detected in avian faeces from the wood partridge
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L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Table 1 Species of Cryptosporidium (modied from Fayer, 2008) Species Cryptosporidium andersoni Cryptosporidium baileyi Cryptosporidium bovis Cryptosporidium canis Cryptosporidium fayeri Cryptosporidium felis Cryptosporidium galli ryptosporidium. hominis Cryptosporidium macropodum Cryptosporidium meleagridis Cryptosporidium molnari Cryptosporidium Cryptosporidium Cryptosporidium Cryptosporidium muris parvum scophthalmi serpentis Author Lindsay et al. (2000) Current et al. (1986) Fayer et al. (2005) Fayer et al. (2001) Ryan et al. (2008) Iseki (1979) Pavlasek (1999) Morgan-Ryan et al. (2002) Power and Ryan (2008) Slavin (1955) Alvarez-Pellitero and Sitja-Bobadilla (2002) Tyzzer (1910) Tyzzer (1912) Alvarez-Pellitero et al. (2004) Levine (1980) (Brownstein et al., 1977) Type host Bos taurus (domestic cattle) Gallus gallus (chicken) Bos taurus (domestic cattle) Canis familiaris (domestic dog) Macropus rufus (red kangaroo) Felis catis (domestic cat) Gallus gallus (chicken) Homo sapiens (human) Macropus giganteus (grey kangaroo) Meleagris gallopavo (turkey) Sparus aurata (gilthead seabream) Dicentrarchus labrax (European seabass) Mus musculus (house mouse) Mus musculus (house mouse) Scophthalmi maximus (turbot) Elaphe guttata (corn snake) Elaphe subocularis (rat snake) Sanzinia madagascarensus (Madagascar boa) Sus scrofa (domestic pig) Varanus prasinus (Emerald monitor) Cavia porcellus (guinea pig) 3
Cryptosporidium suis Cryptosporidium varanii Cryptosporidium wrairi
Ryan et al. (2004) Pavlasek et al. (1995) Vetterling et al. (1971)
Table 2 Cryptosporidium spp. and genotypes that infect humans and other hosts (modied from Fayer, 2008) Species Cryptosporidium andersoni Cryptosporidium baileyi Cryptosporidium canis Cryptosporidium felis Cryptosporidium hominis Cryptosporidium meleagridis Cryptosporidium muris Hosts Cattle, sheep, Bactrian camel, gerbil, multimammate mouse, wood partridge Chicken, duck, Bobwhite quail Dog, fox, coyote Cat, cattle Primates, cattle, sheep, pig, dugong Turkey, chicken, Bobwhite quail, dog, deer mouse Mouse, hamster, squirrel, Siberian chipmunk, wood mouse, bank vole, rock hyrax, Bactrian camel, mountain goat, cat, coyote, ringed seal, bilby, cynomolgus monkey, tawny frogmouth Calf, lamb, horse, alpaca, dog, mouse, raccoon dog, eastern squirrel Pig, cattle Cattle, sheep, ibex grey squirrel, eastern chipmunk, beaver, red squirrel, woodchuck, deer mouse, raccoon deer, mouon sheep, blesbok, nyala, lemur Skunk, raccoon, eastern squirrel, opossum, river otter
Cryptosporidium parvum Cryptosporidium suis Cervine genotype
Skunk genotype
and tawny frogmouth, respectively (Ng et al., 2006), based on PCR. Whether the oocysts in the faeces were due to mechanical transport or an actual infection remains to be determined. Cryptosporidium parvum, the most studied species, was once thought to infect many, if not all, species of mammals. Under experimental conditions one study concluded that it infected chickens (Palkovic and Marousek,
1989), another found it did not infect chickens (Darabus and Olariu, 2003) and still another found it did not infect ducks or geese (Graczyk et al., 1996a, 1997). Other conicting reports add to the confusion regarding the range of host species for C. parvum. One study indicated that C. parvum oocysts from a human infected sh, amphibians, reptiles, birds and mammals (Arcay et al., 1995) whereas another found that C. parvum oocysts from a bovine did not infect sh, amphibians or reptiles but simply passed through the digestive tracts (Graczyk et al., 1996b). Some species of Cryptosporidium appear restricted to one host species: Cryptosporidium wrairi apparently infects only guinea pigs (Gibson and Wagner, 1986). Other species of Cryptosporidium have been found to infect a predominant host species and to a much lesser extent other hosts including humans (Table 2). The nomenclature for Giardia is confusing and needs clarity. The species Giardia agilis, Giardia ardeae, Giardia muris, Giardia microti and Giardia psittaci have been found to infect various animals but not humans (Table 3). The species names Giardia duodenalis, Giardia intestinalis and Giardia lamblia are all used interchangeably in current literature referring to the same organism. For purposes of consistency G. duodenalis is used in this review. Within this species the current trend has been to identify a complex of assemblages based on host specicity. These assemblages are identied based on the analysis of conserved genetic loci (Caccio et al., 2005). Currently, there are seven well dened assemblages of G. duodenalis, designated A through G. Assemblages A and B have the broadest host specicity, having been found to infect humans and various other mammals, including dogs, cats, livestock and wildlife (Karanis and Ey, 1998; Caccio et al., 2005). Assemblage A consists of mostly two subgroups AI and AII, and there is no
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Table 3 Species and assemblages of Giardia (modied from Thompson, 2004) Species Giardia agilis Giardia ardeae Giardia microti Giardia muris Giardia psittaci Giardia duodenalis Assemblage A Author Hegner (1922) Noller (1920) Benson (1908) Benson (1908) Erlandsen and Bemrick (1987) Davaine (1875) Hosts Amphibians Birds Muskrats and voles Rodents Birds
Assemblage B Assemblage Assemblage Assemblage Assemblage Assemblage C D E F G
Humans, primates, dogs, cats, cattle, rodents, wild mammals Humans, primates, dogs, horses, cattle Dogs Dogs Artiodactyls Cats Rodents
clear subgrouping in assemblage B (Monis et al., 1999, 2003; Thompson, 2000; Sulaiman et al., 2003; Read et al., 2004; Wielinga and Thompson, 2007). Assemblages C and D have been found to infect only dogs (Hopkins et al., 1997; Monis et al., 1998; Leonhard et al., 2007). Assemblage E has been found to infect only cloven-hooved mammals (Ey et al., 1997). Assemblages F and G have been found to infect only cats and rodents, respectively (Monis et al., 1999). 4. Host specicity of Cryptosporidium and Giardia species and genotypes in animals With some exceptions, most Cryptosporidium and Giardia species and genotypes are host-adapted in nature, having a narrow spectrum of natural hosts. Thus, one species or genotype usually infects only a particular species or group of related animals. Recognizing the zoonotic potential of each species is based upon knowing the host range or host specicity of that species. This can be determined in part by: (i) accurately identifying the species/genotype from the oocyst/cyst in the faeces of naturally infected hosts using molecular methods and (ii) obtaining oocysts or cysts from one host species and feeding those to putative hosts of another species. When feeding these stages results in completion of the life cycle in the putative host and de novo stages are excreted that are genetically identical to those that initiated the infection, the conrmed host range is extended. However, the inability to obtain sucient numbers of oocysts or cysts and diculty in obtaining and/or housing wildlife, or scarce or expensive domesticated animals, limits testing. Both (i) and (ii) rely on molecular methods to clearly identify the species because morphological methods lack the specicity required to distinguish many species and genotypes. For example, oocysts of C.
parvum, Cryptosporidium hominis, C. meleagridis and Cryptosporidium bovis have no apparent internal features that are unique among them and they overlap in size, diering only at the extremes by a few tenths of a micrometre. The oocyst size ranges for each species are 4.86.0 4.8 5.4 lm, 4.45.9 4.45.4 lm, 4.56.0 4.25.3 lm and 4.85.4 4.24.8 lm, respectively (Fayer et al., 2005; Fayer, 2008). Likewise, cysts of the assemblages of G. duodenalis are dicult or impossible to distinguish from one another by microscopy (Filice, 1952). Conrmation of infection is complicated when only one or two faecal specimens serve as the source of oocysts or cysts because it can be argued that these stages were ingested and simply passed through the gut without actually infecting the host. This has been demonstrated experimentally (Graczyk et al., 1996a). For humans, even when it appears conclusive that there is an infection with a potentially zoonotic species or genotype one might argue that the infection was acquired from a human source rather than an animal and therefore transmission is anthroponotic not zoonotic. Because the two foregoing issues cannot always be resolved by investigators we are even less able to resolve these issues by review of their publications, therefore, interpretation of some of the examples presented as zoonotic infections in this review will fall in part to the judgment of the reader. 4.1. Cryptosporidium Surveys conducted in cattle, sheep, pigs, cats, dogs, kangaroos, squirrels, other wild mammals, Canada geese and reptiles have shown that most animal species are infected with only a few host-adapted Cryptosporidium species or genotypes (Iseki, 1979; Asahi et al., 1991; Guselle et al., 2003; Jellison et al., 2004; Power et al., 2004; Ryan et al., 2004, 2005; Xiao et al., 2004c; Zhou et al., 2004a,b; Fayer et al., 2006c; Feng et al., 2007a; Langkjaer et al., 2007). The existence of host-adapted Cryptosporidium species or genotypes indicates that cross transmission of Cryptosporidium among dierent groups of animals is usually limited. Cross-species transmission is possible when animals share a similar habitat and/or the parasite is biologically capable of infecting multiple host species. Two genotypes that appear to t this description are the skunk genotype and the cervine genotype. The skunk genotype has been detected in faeces of skunks, raccoons, squirrels and opossums (Feng et al., 2007a). The cervine genotype has been detected in faeces of domestic and wild ruminants (domesticated sheep, mouon sheep, blesbok, nyala and deer), rodents (squirrels, chipmunks, woodchucks, beavers and deer mice), carnivores (raccoons) and primates (lemurs and humans) (Perz and Le Blancq, 2001; Ong et al., 2002; da Silva et al., 2003; Ryan et al., 2003; Ryan et al., 2005; Blackburn et al., 2006; Feltus et al., 2006; Leoni et al., 2006; Nichols et al., 2006; Soba et al., 2006; Trotz-Williams et al., 2006; Feng et al., 2007a).
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Cryptosporidium parvum has received the most attention with regard to cross-species transmission. Although C. parvum was once thought to infect all mammals, genetic characterisation of Cryptosporidium specimens have mostly failed to detect this species in wild mammals (Zhou et al., 2004a; Feng et al., 2007a). It is now generally accepted that C. parvum (previously referred to as genotype II or the bovine genotype) primarily infects ruminants and humans. Even in cattle, only calves less than 2 months of age (primarily monogastric) are frequently infected with this species. The prevalence in beef calves is often lower than in dairy calves, even when raised in similar conditions (Kvac et al., 2006). Most infections in older dairy calves are caused by C. bovis and the deer-like genotype, and infections in mature cattle are mostly with C. andersoni (Santin et al., 2004; Fayer et al., 2006c; Feng et al., 2007b; Langkjaer et al., 2007). Therefore, the major contributors of zoonotic C. parvum appear to be dairy calves less than 2 months of age. Cryptosporidium parvum has only been detected in small numbers in other farm animals. Two recent studies in Australia and the USA report that oocysts of C. parvum are not commonly detected in sheep faeces, which more often contain oocysts of the Cryptosporidium cervine genotype and other genotypes (Ryan et al., 2005; Santin et al., 2007). Although C. parvum has been detected in a few horses and alpacas, its prevalence is not known (Grinberg et al., 2003; Hajdusek et al., 2004; Chalmers et al., 2005b; Starkey et al., 2007; Twomey et al., 2008) and horses are known to be infected with a Cryptosporidium horse genotype (Ryan et al., 2003). Natural C. parvum infections have been found occasionally in other animals such as mice, raccoon dogs and dogs (Morgan et al., 1999; Matsubayashi et al., 2004; Giangaspero et al., 2006). Companion animals are most often infected with hostspecic Cryptosporidium spp. Thus, dogs are almost exclusively infected with Cryptosporidium canis (Morgan et al., 2000; Satoh et al., 2006; Huber et al., 2007; RimhanenFinne et al., 2007) and most cats are infected with Cryptosporidium felis, although C. muris was found in faeces from two cats (Fayer et al., 2006a; Pavlasek and Ryan, 2007; Santin et al., 2006; Rimhanen-Finne et al., 2007). Because C. canis and C. felis infections are infrequently reported for humans, despite close and widespread contact with dogs and cats, the role of dogs and cats in the transmission of human cryptosporidiosis appears quite limited. 4.2. Giardia Of all the species of Giardia only G. duodenalis has been found in humans, livestock and companion animals. Most of the animals in these groups have unique G. duodenalis assemblages, but some have been found to harbour assemblages A and/or B, which also infect humans. Most cattle, sheep and pigs are infected with G. duodenalis assemblage E (Table 4). A signicant number of cattle, however, are also infected with assemblage A. In contrast, assemblage B was found in a small number of cattle in a few studies, and
other assemblages have never been convincingly found in cattle (Table 4). The only exception is in New Zealand, where limited studies indicate that assemblages A and B appeared to be common in cattle and assemblage E was largely absent (Hunt et al., 2000; Learmonth et al., 2003). There are no age-associated dierences in the distribution of assemblages A and E in cattle. Four multi-state prevalence studies for G. duodenalis in the eastern USA involving nearly 2,000 cattle from birth to adulthood reported that assemblage E was found in 28% of preweaned calves, 45% of post-weaned calves, 33% of heifers and 25% of adult cows, whereas assemblage A was detected in 6% of preweaned calves, 7% of post-weaned calves, 3% of heifers and 2% of adult cows (Trout et al., 2004, 2005, 2006b, 2007). For sheep, studies have all identied a predominance of assemblage E in both lambs and ewes, with assemblage A identied infrequently (Table 4). Assemblage B has rarely been found in sheep. Although an outbreak of giardiasis in lambs with severe weight loss and some mortality was attributed to assemblage B, this conclusion was based on PCR analysis of only two specimens (Aloisio et al., 2006). Results of a study of pigs indicated a pattern similar to that of cattle and sheep (Langkjaer et al., 2007). In the only survey conducted of horses, albeit just nine animals, only assemblages A and B were found (Traub et al., 2005). Dogs are infected with a broader range of G. duodenalis assemblages. Dogs in Australia were found to be infected with assemblages A, B, C and D (Monis et al., 1998). The same assemblages have been found in dogs in other countries with a dominance of assemblages C and D (Table 5). Many studies have also shown modest to high prevalence of assemblage A (Table 5). In contrast, infection with assemblage B has rarely been found in dogs (Read et al., 2004; Traub et al., 2004). Cats are infected with assemblages A and F, with the cat-specic assemblage F found more frequently than assemblage A (Table 5). Although one study identied almost all known assemblages (A, B, C, D and E) except F in cats (Read et al., 2004) there was a high level of discrepancy in genotyping results of animal samples between the two genotyping tools used in the study. Assemblage A was found in a ferret in a pet shop (Abe et al., 2005). Little information is available on the prevalence of G. duodenalis assemblages infecting wildlife. Limited reports showed mostly the presence of assemblage A and the lack of assemblage E in wild cervids. Two cases of giardiasis in a white-tailed deer in the USA and a roe deer in the Netherlands were identied as assemblage A (Trout et al., 2003; van der Giessen et al., 2006). Likewise, only assemblage A was found in 15 moose and nine reindeer in Norway (Robertson et al., 2007), eight fallow deer in Italy (Lalle et al., 2007), one fox and three kangaroos in Australia (McCarthy et al., 2008). Assemblages B, C and D are found in other wild mammals. Of 15 positive faecal specimens from beavers and
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Table 4 Giardia duodenalis genotypes in farm animals Animal Location Sample size Assemblage A Cattle Cattle Cattle Cattle Cattle (preweaned calves) Cattle (weaned calves) Cattle Cattle Cattle (12 years) Cattle (cows) Cattle Cattle Cattle Cattle Cattle Cattle Cattle (preweaned calves) Cattle Cattle (preweaned calves) Cattle Cattle Italian water bualo Sheep Sheep Sheep Sheep Sheep Goat Alpaca Pig Horse Italy Portugal Denmark Belgium USA USA USA USA USA USA Canada Canada Canada Brazil Taiwan Japan Vietnam Australia Australia New Zealand New Zealand Italy Italy Spain USA Mexico Australia Spain USA Denmark USA and Australia 24 14 145 101 164 237 58 7 204 144 42 14 60 5 4 5 17 16 31 15 48 8 5 12 14 14 46 39 3 82 9 12 2 8 16 25 31 8 18 9 1 6 35 1 2 1 1 B 5 1 E 3 11 133 54 139 196 48 7 186 135 41 14 25 4 2 4 16 16 31 Others A+B (2), A+E (2) 4 unknown A+E (31) Lalle et al. (2005b) Mendonca et al. (2007) Langkjaer et al. (2007) Geurden et al. (2008a) Trout et al. (2004) Trout et al. (2005) Feng et al. (in press) Sulaiman et al. (2003) Trout et al. (2006b) Trout et al. (2007) Appelbee et al. (2003) Uehlinger et al. (2006) Coklin et al. (2007) Souza et al. (2007) Hsu et al. (2007) Itagaki et al. (2005) Geurden et al. (in press) Read et al. (2002) Becher et al. (2004) Learmonth et al. (2003) Caccio et al. (2007) Giangaspero et al. (2005) Castro-Hermida et al. (2007) Santin et al. (2007) Di Giovanni et al. (2006) Ryan et al. (2005) Ruiz et al. (in press) Trout et al. (in press) Langkjaer et al. (2007) Traub et al. (2005) Reference
A+E (2)
11 26 2 5 1 11 3 10 4
4 22 6 1 11 13 14 33 39 65 6
2 unknown
C (2) and unknown (1)
Table 5 Giardia duodenalis genotypes in domestic pets Animal Location Sample size Assemblage A Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Dog Cat Cat Cat Cat Cat Cat Cat Italy Italy Germany Germany Hungary India Japan Japan Thailand Australia Australia USA Mexico Mexico Brazil Brazil Italy USA USA Brazil Columbia Japan Australia 17 21 55 150 15 7 4 24 13 11 9 15 5 11 27 7 10 17 8 from 1 colony 19 3 3 18 2 6 33 4 5 14 5 1 4 7 7 7 10 6 8 20 2 2 1 1 10 4 15 4 6 3 1 2 A+D (3) A+B (3), A+D (1) B C 11 1 5 54 5 D 1 12 2 83 9 F Others A+C (2), C+D (1) A+D (1) A+C (15) C+D (8), A+D (1) C+D (1) Berrilli et al. (2004) Lalle et al. (2005b) Leonhard et al. (2007) Barutzki et al. (2007) Szenasi et al. (2007) Traub et al. (2004) Abe et al. (2003) Itagaki et al. (2005) Inpankaew et al. (2007) Monis et al. (1998, 2003) Read et al. (2002) Sulaiman et al. (2003) Lalle et al. (2005a) Eligio-Garcia et al. (2005) Souza et al. (2007) Volotao et al. (2007) Papini et al. (2007) Vasilopulos et al. (2007) Fayer et al. (2006a) Souza et al. (2007) Santin et al. (2006) Itagaki et al. (2005) Read et al. (2004) Reference
A+B (1) A4 (probably C or D) (4)
11 8 11 3 3 2 2 7 E (1)
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muskrats trapped in Maryland, USA, assemblage B was found in seven beavers and ve muskrats, and G. microti was found in three other muskrats (Sulaiman et al., 2003). Of 62 beavers trapped in Massachusetts, USA, four had assemblage B (Fayer et al., 2006b). One rabbit was found infected with assemblage B (Sulaiman et al., 2003). Among seven coyotes in the USA positive for G. duodenalis, one had assemblage B, three had assemblage C, and three had assemblage D (Trout et al., 2006a). In contrast, assemblage A was found in two gorillas in Uganda (Graczyk et al., 2002) and assemblage B was found in three wild Japanese monkeys (Macaca fuscata) (Itagaki et al., 2005). 5. Cryptosporidium and Giardia species and genotypes in humans 5.1. Cryptosporidium Cryptosporidium parvum was once considered the only Cryptosporidium species to infect humans. The use of genotyping tools in the late 1990s identied two genotypes (I and II) of C. parvum, which eventually became C. hominis and C. parvum senso stricto, both infectious for immunocompetent and immunocompromised persons (Xiao et al., 2004a,b; Caccio, 2005). Subsequently, the use of ssrRNA-based genotyping tools revealed the presence of several other species, including C. canis, C. felis and C. meleagridis in human faeces (Pieniazek et al., 1999; McLauchlin et al., 2000; Alves et al., 2001; Guyot et al., 2001; Xiao et al., 2001; Caccio et al., 2002a; Gatei et al., 2002b, 2006; Tiangtip and Jongwutiwes, 2002; Cama et al., 2003; Leoni et al., 2006). Still other species found in human faeces, but in fewer cases, include C. muris (Katsumata et al., 2000; Guyot et al., 2001; Gatei et al., 2002a, 2006; Palmer et al., 2003; Muthusamy et al., 2006) and Cryptosporidium suis (Xiao et al., 2002; Leoni et al., 2006; Nichols et al., 2006). In addition, several genotypes of Cryptosporidium have been detected in faeces from patients experiencing cryptosporidiosis including the cervine genotype (Ong et al., 2002; Blackburn et al., 2006; Feltus et al., 2006; Leoni et al., 2006; Nichols et al., 2006; Soba et al., 2006; Trotz-Williams et al., 2006), a C. suis-like genotype (Ong et al., 2002), a C. andersoni-like genotype (Leoni et al., 2006; Morse et al., 2007), the chipmunk genotype I (W17) (Feltus et al., 2006), the skunk genotype (Nichols et al., 2006), and the C. hominis monkey genotype (Mallon et al., 2003a). Because these genotypes were detected in microscopically positive faeces from patients it is improbable that these persons simply had their faeces examined around 4963 h (mean gut transit time; Probert et al., 1995) after they ingested oocysts that transited the gastrointestinal tract. Among the human-pathogenic Cryptosporidium spp., C. hominis and C. parvum are responsible for most human cases of infection (Xiao and Ryan, 2004). Geographic dierences have been reported in disease burdens
attributed to these two species. In the UK, several earlier large scale studies all found that C. parvum was responsible for slightly more infections than C. hominis (McLauchlin et al., 2000; Hunter et al., 2003; Smerdon et al., 2003; Sopwith et al., 2005; Leoni et al., 2006). A more recent study in the UK found that of 13,112 cases of cryptosporidiosis 50.3% were associated with C. hominis and 45.6% were associated withC. parvum (Nichols et al., 2006). Likewise, although earlier studies generally showed a higher prevalence of C. parvum than C. hominis in humans in other European countries, more recent studies have shown a slightly higher prevalence of C. hominis than C. parvum. Thus, in the Netherlands, 91 human isolates consisted of 70% C. hominis, 19% C. parvum, a 10% mixture of C. hominis and C. parvum, and 1% C. felis (Wielinga et al., 2008). In Spain, Llorente et al. (2007) detected C. hominis in 59 of 92 immunocompetent children and 10 of 16 HIV-infected adults (63.8%), and C. parvum, in 28 children and six adults (31.5%); C. parvum was signicantly more frequent in children from rural areas. In general C. hominis has been associated with more infections than C. parvum in the USA, Canada, Australia, Japan and developing countries where molecular methods have been used to identify specimens (Peng et al., 1997; Morgan et al., 1998; Sulaiman et al., 1998; Ong et al., 1999, 2002; Xiao et al., 2004a) although in New Zealand 46.8% of 423 cases were associated with C. hominis and 52.7% were associated with C. parvum (Learmonth et al., 2004). A much higher prevalence of C. parvum is seen in humans in the Middle East. In highly urbanised Kuwait City, almost all cryptosporidiosis cases in children were caused by C. parvum (Sulaiman et al., 2005). In Iran seven of eight HIV patients and four of seven children had cryptosporidiosis caused by C. parvum and the others had C. hominis (Meamar et al., 2007). In Turkey, all four cases of cryptosporidiosis in children had C. parvum (Tamer et al., 2007). 5.2. Giardia Of the established Giardia spp. and G. duodenalis assemblages, only G. duodenalis assemblages A and B are known to infect humans. Assemblage F was reported in humans in one study, but this was likely the result of technical errors (Gelanew et al., 2007). Because both assemblages (A and B) have also been found to infect animals, zoonotic transmission has long been suspected to play a role in epidemiology of human giardiasis. The distribution of these two assemblages in humans varies among studies, sometimes within the same country (see Caccio et al., 2005, for review). The number of molecular epidemiological studies of giardiasis in humans is very small, and do not demonstrate clear geographic or socioeconomic dierences in the distribution of assemblages A and B, or clearly indicate the role of zoonotic infections in human giardiasis.
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6. Molecular epidemiological evidence for zoonotic transmission of cryptosporidiosis and giardiasis 6.1. Cryptosporidium Geographic dierences in the distribution of C. parvum and C. hominis infections within a country support the likelihood of zoonotic cryptosporidiosis. This situation is observed in the USA, the UK and New Zealand where C. hominis infection is more common in urban areas and C. parvum is more common in rural areas (McLauchlin et al., 1999, 2000; Learmonth et al., 2004; Feltus et al., 2006). In the UK, C. hominis infection was found more often in persons with a history of foreign travel (McLauchlin et al., 2000; Goh et al., 2004; Hunter et al., 2004, 2007). In an extensive analysis of human cases of cryptosporidiosis Sopwith et al. (2005) reported that from 1996 to 2000 elevated rates of infection in the North West Region of England (13% of the population) was responsible for 3142% of all cases reported in England and Wales and might have skewed national data for the UK, especially the spring peak caused by C. parvum. The coincidental timing of a foot-and-mouth epidemic in the UK in 2001 and the decrease in the number of cases in spring that year led to speculation that the enforced restriction of farm visits and culling of farm animals was responsible for the great reduction in cases associated with C. parvum after 2001 (Hunter et al., 2003; Smerdon et al., 2003). It appears more likely that the decrease was due to measures taken by the water supplier in the North West Region to improve treatment of drinking water by coagulation and ltration and to restrict livestock from water catchment areas (Sopwith et al., 2005; Lake et al., 2007). The role of zoonotic infections in human cryptosporidiosis in developing countries appears much less important than in industrialised nations. Studies conducted in Brazil, India, Kenya, Malawi, Peru, Thailand, South Africa and Vietnam have shown that 7090% of infections in humans in these developing countries result from C. hominis (Peng et al., 2001, 2003a; Xiao et al., 2001; Leav et al., 2002; Tiangtip and Jongwutiwes, 2002; Cama et al., 2003; Gatei et al., 2003, 2006, 2007; Tumwine et al., 2003, 2005; Das et al., 2006; Muthusamy et al., 2006; Bushen et al., 2007). Because the prevalence of C. parvum in human cases of cryptosporidiosis is much lower, this strongly suggests that zoonotic infection is much less common in developing countries than in industrialised countries. The number of C. parvum infections in humans attributable to zoonotic transmission remains unclear because the source of C. parvum in humans can be of bovine or human origin. Results of sequence analyses of the 60 kDa glycoprotein (GP60) gene support the probable zoonotic transmission in industrialised nations. One major GP60 C. parvum subtype family, IIa, is common in humans in rural areas in the USA and in Europe (Glaberman et al., 2002; Alves et al., 2003, 2006; Stantic-Pavlinic et al., 2003; Chal-
mers et al., 2005a; Feltus et al., 2006). Many of the IIa subtypes found in humans have also been found in calves in the same area. For example, in Portugal one major C. parvum subtype in humans, IIaA15G2R1, is the predominant subtype in calves and zoo ruminants (Alves et al., 2003, 2006). Likewise, in Northern Ireland, most of the common IIa subtypes found in calves have been found in human outbreaks or sporadic cases (Glaberman et al., 2002; Thompson et al., 2007). In Wisconsin, USA, most of the C. parvum subtypes found in humans were also found in calves in neighbouring Michigan and Ontario (Peng et al., 2003b; Feltus et al., 2006; Trotz-Williams et al., 2006). In an apple cider-associated outbreak of cryptosporidiosis in Ohio, USA, all patients had C. parvum subtype IIaA15G2R1 or IIaA17G2R1, and the latter was found in the apple cider (Blackburn et al., 2006). Subtype IIaA17G2R1 is rare in the USA, having been reported only in some calves in Ohio and Vermont (Xiao et al., 2007b). Despite evidence of the presence of IIa subtypes in humans and cattle in the same areas, there is minimal molecularly based epidemiological evidence quantifying the extent of zoonotic transmission. Another less common bovine C. parvum subtype family, IId, might potentially be responsible for some zoonotic infections in industrialised nations. In southern Europe (Portugal, Italy, Serbia and Hungary), although IIa subtypes were the dominant C. parvum in calves, IId subtypes were found occasionally (Alves et al., 2003, 2006; Wu et al., 2003; Misic and Abe, 2006; Plutzer and Karanis, 2007). Some IId subtypes have been found in HIV+ persons in Portugal (Alves et al., 2003, 2006). About half the C. parvum infections in children in Kuwait City are IId subtypes, but transmission appears to be anthroponotic in origin (Sulaiman et al., 2005). IId subtypes of C. parvum have not been found in cattle or humans in the UK, USA, Canada or Australia (Glaberman et al., 2002; Peng et al., 2003b; Chalmers et al., 2005a; Trotz-Williams et al., 2006; Thompson et al., 2007; Xiao et al., 2007b). Multilocus typing data provide evidence of zoonotic transmission of C. parvum in Wales and the North West Region of England (Hunter et al., 2007). At the ML1, ML2 and GP60 loci, there were signicant dierences in C. parvum isolates from persons who had contact with farm animals and those with no animal contact before the onset of illness (Hunter et al., 2007). At the ML1 and ML2 loci, signicantly more persons with C. parvum subtype ML1242 and ML2-223-237 had farm animal contact than those with ML1-227 and ML2-193 or 197, respectively. Similarly, at the GP60 locus, specimens from patients with farm animal contact generated signicantly greater PCR product sizes than those who had no animal contact. Not all C. parvum infections in humans result from zoonotic transmission. In Portugal, the genetic diversity of C. parvum is much higher in HIV+ persons than in calves or other ruminants, and one of the three C. parvum subtype families, IIc, has never been found in animals. The anthroponotic nature of the C. parvum IIc subtype family is sup-
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ported by subtyping studies of human and bovine cryptosporidiosis in Portugal, USA, Canada, UK and Australia. In urban areas in the USA, IIc subtypes are responsible for most human C. parvum infections (Xiao et al., 2004b). In European countries such as Portugal and the UK, both IIa and IIc are fairly common in humans (Alves et al., 2003, 2006). Multilocus typing data also provide evidence of anthroponotic transmission of C. parvum in Europe. Analyses of three minisatellite and four microsatellite markers identied three groups of C. parvum in humans and cattle in Scotland, with two small groups exclusively found in humans and one large group in both humans and calves (Mallon et al., 2003a,b). Similar ndings in England and Wales were based on three of the same microsatellite markers (Leoni et al., 2007). As in Portugal, based on GP60 gene ndings, multilocus data conrmed that humans in Scotland were infected with signicantly wider spectra of C. parvum subtypes than were cattle, indicating that some human C. parvum infections were not related to subtypes found in cattle (Grinberg et al., 2008). In contrast, lower genetic diversity of C. parvum was observed in humans than in animals in France, and there was no host restriction of C. parvum populations (Ngouanesavanh et al., 2006). It is not clear whether the omission of some more polymorphic markers such as GP60 in the French study has contributed to this dierent observation. The anthroponotic IIc subtypes of C. parvum are responsible for most human infections in developing countries (Leav et al., 2002; Peng et al., 2003a; Xiao et al., 2004a; Xiao and Ryan, 2004; Akiyoshi et al., 2006) whereas the zoonotic IIa subtypes are more common in European countries, Australia and the USA. In some regions such as Lima, Peru, IIc subtypes are the only C. parvum found in humans. In developing countries such as Malawi and Kenya, the anthroponotic C. parvum subtype family IIe is found (Peng et al., 2003a; Xiao et al., 2004a; Xiao and Ryan, 2004; Cama et al., 2007). In Uganda, several new C. parvum subtype families are present in humans (Akiyoshi et al., 2006). Most of these studies were done in urban areas but a study in Malawi has shown a higher rate of human C. parvum infection in rural areas than in urban areas (Morse et al., 2007); unfortunately subtyping was not done. An earlier subtyping study found almost exclusive anthroponotic transmission of cryptosporidiosis in the country (Peng et al., 2003a). Whether C. meleagridis, C. canis, C. felis and C. muris are predominantly transmitted in developing countries zoonotically remains unclear. Using C. hominis and C. parvumspecic genotyping tools, the analysis of C. canis- and C. felis-infected specimens from HIV+ persons in Lima, Peru revealed concurrent presence of C. hominis and C. parvum IIc subtype family in six of 21 patients (Cama et al., 2006). There are no multilocus subtyping studies to determine whether there is any host segregation in C. canis or C. felis, although an earlier study of a small number of human and bird specimens failed to show this in C. meleagridis (Gla-
berman et al., 2001). Transmission of C. canis between humans and a dog, however, has been speculated in a recent report (Xiao et al., 2007a). In one household, two diarrhoeic children and one dog were diagnosed during the same period having cryptosporidiosis by microscopic examinations of faecal smears stained with a modied acid-fast stain. Cryptosporidium canis was found in faeces of all three by PCR-restriction fragment length polymorphism (RFLP) and DNA sequence analysis of the ssrRNA gene. The direction of the C. canis transmission, however, was not clear. 6.2. Giardia Because humans are infected only with G. duodenalis assemblages A and B and both genotypes have been found in animals, studies on zoonotic transmission of giardiasis have concentrated on these two genotypes. This especially applies to assemblage A, detected in faeces from many mammals (Tables 4 and 5). Some wild animals such as beavers and muskrats have a high prevalence of assemblage B, and these animals historically have been considered important contamination sources of waterborne giardiasis (see Section 7). Few studies have compared Giardia isolates from humans and animals living in the same locality or household. In Aboriginal communities in Australia ssrRNA gene sequences from 13 humans and nine dogs identied human isolates in genetic groups 1 and 2, and dog isolates in groups 3 and 4 (Hopkins et al., 1997). Only one dog isolate contained groups 2 and 3, suggesting that zoonotic transmission between humans and dogs, if present, was infrequent. In Bangkok, faeces were collected from 204 humans and 229 dogs from 20 temples and surrounding communities. Of 13 Giardia isolates from dogs most were assemblage A, followed by D, B and C, whereas three isolates from humans were assemblages A and B. One dog and two monks in the same monastery had assemblage A (Inpankaew et al., 2007). In two households in a village in northern India the same assemblage A or B subtype was found in both humans and dogs living in the same household (Traub et al., 2003, 2004). In Brazil a child with giardiasis and her dog were both reported to be infected with subtype AI (Volotao et al., 2007). Although assemblage A has been considered the most important G. duodenalis genotype involved in zoonotic giardiasis, subtyping data do not support widespread ndings of zoonotic transmission. The two most common subtypes of assemblage A, AI and AII, dier signicantly in host preference. Humans are mostly infected with AII, although AI is also seen in some areas or studies (Table 6). In contrast, animals are mostly infected with AI, although the AII subtype is seen occasionally (Table 7). Based on the b-giardin gene, subtype AIII has been found in a few humans (Table 6). This could be due to the higher resolution of the locus, because the b-giardin AIII subtype was linked to AII at the glutamate dehydrogenase (GDH)
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Table 6 Subtypes of Giardia duodenalis assemblage A in humans Location Sample size Subtypes AI Italy Italy England France Mexico Mexico Nicaragua Brazil Brazil Peru Korea China China Bangladesh Philippines Australia Ethiopia
a
Reference AII 7 10 12 8 19 3 2 29 6 3 4 2 20 47 5 5 AIII 3 2 Others 6 AII+AIII (1) Lalle et al. (2005b) Caccio et al. (2002b) Amar et al. (2002) Bertrand et al. (2005) Ponce-Macotela et al. (2002) Lalle et al. (2005a) Lebbad et al. (in press) Volotao et al. (2007) Souza et al. (2007) Sulaiman et al. (2003) Lee et al. (2006) Lee et al. (2006) Lu et al. (2002) Haque et al. (2005) Yason and Rivera (2007) Read et al. (2004) Gelanew et al. (2007)
17 13 12 8 19 17 16 62 29 6 3 4 2 29 50 9 23
15 60
2 13a
8 3 4 1
AI+AII (1)
16
AII at glutamate dehydrogenase locus.
Table 7 Subtypes of Giardia duodenalis assemblage A in animals Animal Location Sample size Subtypes AI Cattle Cattle Cattle Cattle Water bualo Sheep Pig Horse Dog Dog Dog Dog Cat Cat Cat
a
Reference AII 2 AIII Mendonca et al. (2007) Langkjaer et al. (2007) Souza et al. (2007) Feng et al. (in press) Caccio et al. (2007) Giangaspero et al. (2005) Langkjaer et al. (2007) Traub et al. (2005) Leonhard et al. (2007) Lalle et al. (2005a) Volotao et al. (2007) Traub et al. (2004) Vasilopulos et al. (2007) Souza et al. (2007) Read et al. (2004)
Portugal Denmark Brazil USA Italy Italy Denmark USA and Australia Germany Mexico Brazil India USA Brazil Australia
2 8 1 10 2 5 10 4 33 5 7 5 6 8 6
8 1 3 2 5 10 3 33 4 7 2 6 8 6
6a
1 1 3
Appeared on one farm briey.
locus in a study that used both genotyping tools (Lebbad et al., in press). There are no clear geographic dierences in the distribution of the two common assemblage A subtypes in humans. Although AI was detected in humans in high frequency in two studies in South America, two other studies conducted in the same countries found only AII in humans (Table 6). Increasing the typing resolution and further epidemiological studies are needed to determine whether the occasional human AI infections are results of anthroponotic or zoonotic transmission. 7. Epidemiological evidence for zoonotic cryptosporidiosis and giardiasis The strongest epidemiological evidence for zoonotic transmission of cryptosporidiosis is from investigations
associating cattle with outbreaks in veterinary students in contact with infected young calves, animal researchers in contact with infected young calves, and children attending agricultural camps and fairs (Preiser et al., 2003; Smith et al., 2004; Kiang et al., 2006). In case-control studies in industrialised nations, contact with cattle was implicated as a risk factor for human cryptosporidiosis (Robertson et al., 2002; Goh et al., 2004; Hunter et al., 2004; Roy et al., 2004; Hunter and Thompson, 2005). In the UK, cryptosporidiosis case numbers are higher in areas with a high estimate of Cryptosporidium oocysts applied to land from manure (Lake et al., 2007). Thus cattle, especially dairy calves, are likely the major reservoir for C. parvum in some areas. In contrast, few epidemiological studies have implicated sheep and companion animals as a source of human cryptosporidiosis (Molbak et al., 1994; Duke
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et al., 1996; Glaser et al., 1998; Katsumata et al., 1998; Robinson and Pugh, 2002; Goh et al., 2004). Little epidemiological evidence exists that strongly supports the importance of zoonotic transmission of giardiasis to humans. In New Zealand, case-control studies of giardiasis did not identify contact with pets as a risk factor for children or adults, although contact with farm animals was associated with an increased risk of infection for adults (Hoque et al., 2002, 2003), Also in New Zealand, the prevalence of giardiasis was higher in rural than urban areas (Mitchell et al., 1993). In the UK, farm visitation was frequent among case patients but specied exposure to dogs, cats, horses, cattle and sheep was not signicant (Stuart et al., 2003). One case-control study in eastern England found associations with exposure to farm animals and pets, particularly pigs, dogs and cats (Warburton et al., 1994). Other studies in the USA, Canada and UK have not found such associations (Mathias et al., 1992; Dennis et al., 1993; Gray et al., 1994). Although giardiasis aects persons in all age groups, the number of reported cases in the USA was highest among children aged 19 years and adults aged 3039 years (Hlavsa et al., 2005; Yoder and Beach, 2007). A marked onset of illness was reported in early summer through early autumn, with a doubling in giardiasis during summer, coinciding with increased outdoor activities such as swimming (essentially communal bathing venues) and camping (Hlavsa et al., 2005). Beavers are probably the most accused animal source of giardiasis for humans in the USA. often resulting from investigations of waterborne outbreaks and reports by hikers and campers who became infected and recalled drinking water from streams or lakes. The rst accusation began in 1976 with an outbreak in Camas, Washington, USA when 128 townspeople had laboratory-conrmed giardiasis. A questionnaire survey revealed that 3.8% of residents had clinical giardiasis, whereas none of 318 residents in a control town were ill. Giardia cysts were recovered from water entering the city water treatment system and also from two storage reservoirs containing chlorinated and ltered stream water. Trapping in the watershed yielded three beavers infected with Giardia that was infective for beagle pups (Dykes et al., 1980). Similar conclusions were made from investigations of waterborne giardiasis outbreaks in New Hampshire and Nevada, USA, largely based on nding Giardia cysts in beavers caught in source watersheds (Lopez et al., 1980; Navin et al., 1985). These reports lack hard evidence of involvement in human infections and merely report circumstantial evidence based on beavers found at contaminated sites; in some cases the beavers were infected. The roles of other animals and humans are virtually omitted from such reports and the possible role of humans as a source of infection for beavers is rarely addressed. In case-control studies, the evidence for an association between drinking wilderness water and acquiring giardiasis is also minimal (Welch, 2000).
8. Perspective The use of molecular epidemiological tools has signicantly changed our understanding of zoonotic transmission of Cryptosporidium spp. and Giardia spp. Genotyping and subtyping data have clearly demonstrated the presence of anthroponotic as well as zoonotic Cryptosporidium types in humans in industrialised nations. The latter is especially true in rural areas of Europe, New Zealand and North America. In contrast, transmission of cryptosporidiosis appears largely anthroponotic in developing countries. These molecular epidemiological data have already shown that zoonotic transmission of Cryptosporidium is less common than once perceived. Nevertheless, more usage of subtyping analysis in case-control studies is needed to accurately assess the extent of zoonotic transmission of cryptosporidiosis in industrialised nations. The story is clearly dierent with giardiasis, where epidemiological evidence indicates high rates of infection from anthroponotic transmission whereas genotyping and subtyping data point only to the potential role for zoonotic transmission with little or no epidemiological support. Further molecular epidemiological studies of giardiasis in humans, utilising case-control study design and subtyping analysis of specimens from both humans and animals, are needed before more denitive conclusions can be made and possible geographic dierences in the occurrence of zoonotic giardiasis can be detected. Systematic comparisons of assemblage A subtypes and assemblage B at various genetic loci and elucidation of parasite population genetics are also needed to better understand zoonotic transmission of G. duodenalis. Acknowledgments The ndings and conclusions in this report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention. References
Abe, N., Kimata, I., Iseki, M., 2003. Identication of genotypes of Giardia intestinalis isolates from dogs in Japan by direct sequencing of the PCR amplied glutamate dehydrogenase gene. J. Vet. Med. Sci. 65, 2933. Abe, N., Read, C., Thompson, R.C., Iseki, M., 2005. Zoonotic genotype of Giardia intestinalis detected in a ferret. J. Parasitol. 91, 179182. Akiyoshi, D.E., Dilo, J., Pearson, C., Chapman, S., Turnwine, J., Tzipori, S., 2003. Characterization of Cryptosporidium meleagridis of human origin passaged through dierent hosts. Infect. Immun. 71, 18281832. Akiyoshi, D.E., Tumwine, J.K., Bakeera-Kitaka, S., Tzipori, S., 2006. Subtype analysis of Cryptosporidium isolates from children in Uganda. J. Parasitol. 92, 10971100. Aloisio, F., Filippini, G., Antenucci, P., Lepri, E., Pezzotti, G., Caccio, S.M., Pozio, E., 2006. Severe weight loss in lambs infected with Giardia duodenalis assemblage B. Vet. Parasitol. 142, 154158. Alves, M., Matos, O., Pereira Da Fonseca, I., Delgado, E., Lourenco, A.M., Antunes, F., 2001. Multilocus genotyping of Cryptosporidium isolates from human HIV-infected and animal hosts. J. Eukaryot. Microbiol., 17S18S.
ARTICLE IN PRESS
12 L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Cama, V.A., Ross, J.M., Crawford, S., Kawai, V., Chavez-Valdez, R., Vargas, D., Vivar, A., Ticona, E., Navincopa, M., Williamson, J., Ortega, Y., Gilman, R.H., Bern, C., Xiao, L., 2007. Dierences in clinical manifestations among Cryptosporidium species and subtypes in HIV-infected persons. J. Infect. Dis. 196, 684691. Castro-Hermida, J.A., Almeida, A., Gonzalez-Warleta, M., Correia da Costa, J.M., Rumbo-Lorenzo, C., Mezo, M., 2007. Occurrence of Cryptosporidium parvum and Giardia duodenalis in healthy adult domestic ruminants. Parasitol. Res. 101, 14431448. Chalmers, R.M., Ferguson, C., Caccio, S., Gasser, R.B., Abs El-Osta, Y.G., Heijnen, L., Xiao, L., Elwin, K., Hadeld, S., Sinclair, M., Stevens, M., 2005a. Direct comparison of selected methods for genetic categorisation of Cryptosporidium parvum and Cryptosporidium hominis species. Int. J. Parasitol. 35, 397410. Chalmers, R.M., Thomas, A.L., Butler, B.A., Morel, M.C., 2005b. Identication of Cryptosporidium parvum genotype 2 in domestic horses. Vet. Rec. 156, 4950. Coklin, T., Farber, J., Parrington, L., Dixon, B., 2007. Prevalence and molecular characterization of Giardia duodenalis and Cryptosporidium spp. in dairy cattle in Ontario, Canada. Vet. Parasitol. 150, 297305. Darabus, G., Olariu, R., 2003. The homologous and interspecies transmission of Cryptosporidium parvum and Cryptosporidium meleagridis. Pol. J. Vet. Sci. 6, 225228. da Silva, A.J., Caccio, S., Williams, C., Won, K.Y., Nace, E.K., Whittier, C., Pieniazek, N.J., Eberhard, M.L., 2003. Molecular and morphologic characterization of a Cryptosporidium genotype identied in lemurs. Vet. Parasitol. 111, 297307. Das, P., Roy, S.S., Mitradhar, K., Dutta, P., Bhattacharya, M.K., Sen, A., Ganguly, S., Bhattacharya, S.K., Lal, A.A., Xiao, L., 2006. Molecular characterization of Cryptosporidium spp. from children in Kolkata, India. J. Clin. Microbiol. 44, 42464249. Dennis, D.T., Smith, R.P., Welch, J.J., Chute, C.G., Anderson, B., Herndon, J.L., von Reyn, C.F., 1993. Endemic giardiasis in New Hampshire: a case-control study of environmental risks. J. Infect. Dis. 167, 13911395. Di Giovanni, G.D., Betancourt, W.Q., Hernandez, J., Assadian, N.W., Flores Margez, J.P., Lopez, E.J., 2006. Investigation of potential zooanthroponotic transmission of cryptosporidiosis and giardiasis through agricultural use of reclaimed wastewater. Int. J. Environ. Health Res. 16, 405418. Duke, L.A., Breathnach, A.S., Jenkins, D.R., Harkis, B.A., Codd, A.W., 1996. A mixed outbreak of Cryptosporidium and campylobacter infection associated with a private water supply. Epidemiol. Infect. 116, 303308. Dykes, A.C., Juranek, D.D., Lorenz, R.A., Sinclair, S., Jakubowski, W., Davies, R., 1980. Municipal waterborne giardiasis: an epidemiologic investigation. Beavers implicated as a possible reservoir. Ann. Intern. Med. 92, 165170. Eligio-Garcia, L., Cortes-Campos, A., Jimenez-Cardoso, E., 2005. Genotype of Giardia intestinalis isolates from children and dogs and its relationship to host origin. Parasitol. Res. 97, 16. Ey, P.L., Mansouri, M., Kulda, J., Nohynkova, E., Monis, P.T., Andrews, R.H., Mayrhofer, G., 1997. Genetic analysis of Giardia from hoofed farm animals reveals artiodactyl-specic and potentially zoonotic genotypes. J. Eukaryot. Microbiol. 44, 626635. Fayer, R., Trout, J.M., Xiao, L., Morgan, U.M., Lal, A.A., Dubey, J.P., 2001. Cryptosporidium canis n. sp. from domestic dogs. J. Parasitol. 87, 14151422. Fayer, R., Santin, M., Xiao, L., 2005. Cryptosporidium bovis n. sp. (Apicomplexa: Cryptosporidiidae) in cattle (Bos taurus). J. Parasitol. 91, 624629. Fayer, R., Santin, M., Trout, J.M., Dubey, J.P., 2006a. Detection of Cryptosporidium felis and Giardia duodenalis assemblage F in a cat colony. Vet. Parasitol. 140, 4453. Fayer, R., Santin, M., Trout, J.M., DeStefano, S., Koenen, K., Kaur, T., 2006b. Prevalence of microsporidia, Cryptosporidium, and Giardia in beavers (Castor canadensis) in Massachusetts. J. Zoo Wildl. Med. 37, 492497.
Alves, M., Xiao, L., Sulaiman, I., Lal, A.A., Matos, O., Antunes, F., 2003. Subgenotype analysis of Cryptosporidium isolates from humans, cattle, and zoo ruminants in Portugal. J. Clin. Microbiol. 41, 27442747. Alves, M., Xiao, L., Antunes, F., Matos, O., 2006. Distribution of Cryptosporidium subtypes in humans and domestic and wild ruminants in Portugal. Parasitol. Res. 99, 287292. Amar, C.F., Dear, P.H., Pedraza-Diaz, S., Looker, N., Linnane, E., McLauchlin, J., 2002. Sensitive PCR-restriction fragment length polymorphism assay for detection and genotyping of Giardia duodenalis in human feces. J. Clin. Microbiol. 40, 446452. Appelbee, A.J., Frederick, L.M., Heitman, T.L., Olson, M.E., 2003. Prevalence and genotyping of Giardia duodenalis from beef calves in Alberta, Canada. Vet. Parasitol. 112, 289294. Arcay, L., Baez de Borges, E., Bruzual, E., 1995. Cryptosporidiosis experimental en la escala de vertebreados. I.-Infecciones experimentales, II.-Estudio histopatologico. Parasitol. Dia. 19, 2029. Asahi, H., Koyama, T., Arai, H., Kunakoshi, Y., Yamaura, H., Sirasaka, R., Okutoni, K., 1991. Biological nature of Cryptosporidium sp. isolated from a cat. Parasitol. Res. 77, 237240. Barutzki, D., Thompson, R.C., Wielinga, C., Parka, U., Schaper, R., 2007. Observations on Giardia infection in dogs from veterinary clinics in Germany. Parasitol. Res. 101 (Suppl. 1), 153156. Becher, K.A., Robertson, I.D., Fraser, D.M., Palmer, D.G., Thompson, R.C., 2004. Molecular epidemiology of Giardia and Cryptosporidium infections in dairy calves originating from three sources in Western Australia. Vet. Parasitol. 123, 19. Berrilli, F., Di Cave, D., De Liberato, C., Franco, A., Scaramozzino, P., Orecchia, P., 2004. Genotype characterisation of Giardia duodenalis isolates from domestic and farm animals by SSU-rRNA gene sequencing. Vet. Parasitol. 122, 193199. Bertrand, I., Albertini, L., Schwartzbrod, J., 2005. Comparison of two target genes for detection and genotyping of Giardia lamblia in human feces by PCR and PCR-restriction fragment length polymorphism. J. Clin. Microbiol. 43, 59405944. Blackburn, B.G., Mazurek, J.M., Hlavsa, M., Park, J., Tillapaw, M., Parrish, M., Salehi, E., Franks, W., Koch, E., Smith, F., Xiao, L., Arrowood, M., Hill, V., da Silva, A., Johnston, S., Jones, J.L., 2006. Cryptosporidiosis associated with ozonated apple cider. Emerg. Infect. Dis. 12, 684686. Bushen, O.Y., Kohli, A., Pinkerton, R.C., Dupnik, K., Newman, R.D., Sears, C.L., Fayer, R., Lima, A.A., Guerrant, R.L., 2007. Heavy cryptosporidial infections in children in northeast Brazil: comparison of Cryptosporidium hominis and Cryptosporidium parvum. Trans. R. Soc. Trop. Med. Hyg. 101, 378384. Caccio, S., Pinter, E., Fantini, R., Mezzaroma, I., Pozio, E., 2002a. Human infection with Cryptosporidium felis: case report and literature review. Emerg. Infect. Dis. 8, 8586. Caccio, S.M., De Giacomo, M., Pozio, E., 2002b. Sequence analysis of the beta-giardin gene and development of a polymerase chain reactionrestriction fragment length polymorphism assay to genotype Giardia duodenalis cysts from human faecal samples. Int. J. Parasitol. 32, 1023 1030. Caccio, S.M., 2005. Molecular epidemiology of human cryptosporidiosis. Parassitologia 47, 185192. Caccio, S.M., Thompson, R.C., McLauchlin, J., Smith, H.V., 2005. Unravelling Cryptosporidium and Giardia epidemiology. Trends Parasitol. 21, 430437. Caccio, S.M., Rinaldi, L., Cringoli, G., Condoleo, R., Pozio, E., 2007. Molecular identication of Cryptosporidium parvum and Giardia duodenalis in the Italian water bualo (Bubalus bubalis). Vet. Parasitol. 150, 146149. Cama, V., Gilman, R.H., Vivar, A., Ticona, E., Ortega, Y., Bern, C., Xiao, L., 2006. Mixed Cryptosporidium infections and HIV. Emerg. Infect. Dis. 12, 10251028. Cama, V.A., Bern, C., Sulaiman, I.M., Gilman, R.H., Ticona, E., Vivar, A., Kawai, V., Vargas, D., Zhou, L., Xiao, L., 2003. Cryptosporidium species and genotypes in HIV-positive patients in Lima, Peru. J. Eukaryot. Microbiol. 50 (Suppl.), 531533.
ARTICLE IN PRESS
L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Fayer, R., Santin, M., Trout, J.M., Greiner, E., 2006c. Prevalence of species and genotypes of Cryptosporidium found in 12-year-old dairy cattle in the eastern USA. Vet. Parasitol. 135, 105112. Fayer, R., 2008. Biology. In: Fayer, R., Xiao, L. (Eds.), Cryptosporidium and Cryptosporidiosis, second ed. CRC Press and IWA Publishing, Boca Raton, FL, pp. 142. Feltus, D.C., Giddings, C.W., Schneck, B.L., Monson, T., Warshauer, D., McEvoy, J.M., 2006. Evidence supporting zoonotic transmission of Cryptosporidium in Wisconsin. J. Clin. Microbiol. 44, 43034308. Feng, Y., Alderisio, K.A., Yang, W., Blancero, L.A., Kuhne, W.G., Nadareski, C.A., Reid, M., Xiao, L., 2007a. Cryptosporidium genotypes in wildlife from a New York watershed. Appl. Environ. Microbiol. 73, 64756483. Feng, Y., Ortega, Y., He, G., Das, P., Xu, M., Zhang, X., Fayer, R., Gatei, W., Cama, V., Xiao, L., 2007b. Wide geographic distribution of Cryptosporidium bovis and the deer-like genotype in bovines. Vet. Parasitol. 144, 19. Feng, Y., Ortega, Y., Cama, V., Terrell, J., Xiao, L., in press. High intragenotypic diversity of Giardia duodenalis in dairy cattle on three farms. Parasitol. Res. Filice, F.P., 1952. Studies on the cytology and life history of a Giardia from the laboratory rat. Univ. Calif. Publ. Zool. 57, 53146. Gatei, W., Ashford, R.W., Beeching, N.J., Kamwati, S.K., Greensill, J., Hart, C.A., 2002a. Cryptosporidium muris infection in an HIV-infected adult, Kenya. Emerg. Infect. Dis. 8, 204206. Gatei, W., Suputtamongkol, Y., Waywa, D., Ashford, R.W., Bailey, J.W., Greensill, J., Beeching, N.J., Hart, C.A., 2002b. Zoonotic species of Cryptosporidium are as prevalent as the anthroponotic in HIV-infected patients in Thailand. Ann. Trop. Med. Parasitol. 96, 797802. Gatei, W., Greensill, J., Ashford, R.W., Cuevas, L.E., Parry, C.M., Cunlie, N.A., Beeching, N.J., Hart, C.A., 2003. Molecular analysis of the 18S rRNA gene of Cryptosporidium parasites from patients with or without human immunodeciency virus infections living in Kenya, Malawi, Brazil, the UK, and Vietnam. J. Clin. Microbiol. 41, 1458 1462. Gatei, W., Wamae, C.N., Mbae, C., Waruru, A., Mulinge, E., Waithera, T., Gatika, S.M., Kamwati, S.K., Revathi, G., Hart, C.A., 2006. Cryptosporidiosis: prevalence, genotype analysis, and symptoms associated with infections in children in Kenya. Am. J. Trop. Med. Hyg. 75, 7882. Gatei, W., Das, P., Dutta, P., Sen, A., Cama, V., Lal, A.A., Xiao, L., 2007. Multilocus sequence typing and genetic structure of Cryptosporidium hominis from children in Kolkata, India. Infect. Genet. Evol. 7, 197205. Gelanew, T., Lalle, M., Hailu, A., Pozio, E., Caccio, S.M., 2007. Molecular characterization of human isolates of Giardia duodenalis from Ethiopia. Acta Trop. 102, 9299. Geurden, T., Geldhof, P., Levecke, B., Martens, C., Berkvens, D., Casaert, S., Vercruysse, J., Claerebout, E., 2008a. Mixed Giardia duodenalis assemblage A and E infections in calves. Int. J. Parasitol. 38, 259264. Geurden, T., Somers, R., Thanh, N.T., Vien, L.V., Nga, V.T., Giang, H.H., Dorny, P., Giao, H.K., Vercruysse, J., in press. Parasitic infections in dairy cattle around Hanoi, northern Vietnam. Vet. Parasitol. Giangaspero, A., Paoletti, B., Iorio, R., Traversa, D., 2005. Prevalence and molecular characterization of Giardia duodenalis from sheep in central Italy. Parasitol. Res. 96, 3237. Giangaspero, A., Iorio, R., Paoletti, B., Traversa, D., Capelli, G., 2006. Molecular evidence for Cryptosporidium infection in dogs in Central Italy. Parasitol. Res. 99, 297299. Gibson, S.V., Wagner, J.E., 1986. Cryptosporidiosis in guinea pigs, a retrospective study. J. Am. Vet. Med. Assoc. 189, 10331034. Girouard, D., Gallant, J., Akiyoshi, D., Nunnari, J., Tzipori, S., 2006. Failure to propagate Cryptosporidium spp. in cell-free-culture. J. Parasitol. 92, 399400. Glaberman, S., Sulaiman, I.M., Bern, C., Limor, J., Peng, M.M., Morgan, U., Gilman, R., Lal, A.A., Xiao, L., 2001. A multilocus genotypic 13
analysis of Cryptosporidium meleagridis. J. Eukaryot. Microbiol. 48, 19S22S. Glaberman, S., Moore, J.E., Lowery, C.J., Chalmers, R.M., Sulaiman, I., Elwin, K., Rooney, P.J., Millar, B.C., Dooley, J.S., Lal, A.A., Xiao, L., 2002. Three drinking-water-associated cryptosporidiosis outbreaks, Northern Ireland. Emerg. Infect. Dis. 8, 631633. Glaser, C.A., Safrin, S., Reingold, A., Newman, T.B., 1998. Association between Cryptosporidium infection and animal exposure in HIVinfected individuals. J. Acquir. Immune Dec. Syndr. Hum. Retrovirol. 17, 7982. Goh, S., Reacher, M., Casemore, D.P., Verlander, N.Q., Chalmers, R., Knowles, M., Williams, J., Osborn, K., Richards, S., 2004. Sporadic cryptosporidiosis, North Cumbria, England, 19962000. Emerg. Infect. Dis. 10, 10071015. Graczyk, T.K., Craneld, M.R., Fayer, R., Anderson, M.S., 1996a. Viability and infectivity of Cryptosporidium parvum oocysts are retained upon intestinal passage through a refractory avian host. Appl. Environ. Microbiol. 62, 32343237. Graczyk, T.K., Fayer, R., Craneld, M.R., 1996b. Cryptosporidium parvum is not transmissible to sh, amphibians, or reptiles. J. Parasitol. 82, 748751. Graczyk, T.K., Craneld, M.R., Fayer, R., Trout, J., Goodale, H.J., 1997. Infectivity of Cryptosporidium parvum oocysts is retained upon intestinal passage through a migratory water-fowl species (Canada goose, Branta canadensis). Trop. Med. Int. Health 2, 341347. Graczyk, T.K., Bosco-Nizeyi, J., Ssebide, B., Thompson, R.C., Read, C., Craneld, M.R., 2002. Anthropozoonotic Giardia duodenalis genotype (assemblage) a infections in habitats of free-ranging human-habituated gorillas, Uganda. J. Parasitol. 88, 905909. Gray, S.F., Gunnell, D.J., Peters, T.J., 1994. Risk factors for giardiasis: a case-control study in Avon and Somerset. Epidemiol. Infect. 113, 95 102. Grinberg, A., Oliver, L., Learmonth, J.J., Leyland, M., Roe, W., Pomroy, W.E., 2003. Identication of Cryptosporidium parvum cattle genotype from a severe outbreak of neonatal foal diarrhoea. Vet. Rec. 153, 628 631. Grinberg, A., Lopez-Villalobos, N., Pomroy, W., Widmer, G., Smith, H., Tait, A., 2008. Host-shaped segregation of the Cryptosporidium parvum multilocus genotype repertoire. Epidemiol. Infect. 136, 273278. Guselle, N.J., Appelbee, A.J., Olson, M.E., 2003. Biology of Cryptosporidium parvum in pigs: from weaning to market. Vet. Parasitol. 113, 7 18. Guyot, K., Follet-Dumoulin, A., Lelievre, E., Sarfati, C., Rabodonirina, M., Nevez, G., Cailliez, J.C., Camus, D., Dei-Cas, E., 2001. Molecular characterization of Cryptosporidium isolates obtained from humans in France. J. Clin. Microbiol. 39, 34723480. Hajdusek, O., Ditrich, O., Slapeta, J., 2004. Molecular identication of Cryptosporidium spp. in animal and human hosts from the Czech Republic. Vet. Parasitol. 122, 183192. Haque, R., Roy, S., Kabir, M., Stroup, S.E., Mondal, D., Houpt, E.R., 2005. Giardia assemblage A infection and diarrhea in Bangladesh. J. Infect. Dis. 192, 21712173. Hijjawi, N.S., Meloni, B.P., Nganzo, M., Ryan, U.M., Olson, M.E., Cox, P.T., Monis, P.T., Thompson, R.C.A., 2004. Complete development of Cryptosporidium parvum in host-free culture. J. Parasitol. 34, 769777. Hijjawi, N.S., Meloni, B.P., Ryan, U.M., Olsen, M.E., Thompsopn, R.C.A., 2002. Successful in vitro cultivation of Cryptosporidium andersoni: evidence for the existence of novel extracellular stages in the life cycle and implications for the classication of Cryptosporidium. Int. J. Parasitol. 32, 17191726. Hlavsa, M.C., Watson, J.C., Beach, M.J., 2005. Giardiasis surveillanceUSA, 19982002. Morbid. Mortal. Wkly. Rep. Surveill. Summ. 54, 9 16. Hopkins, R.M., Meloni, B.P., Groth, D.M., Wetherall, J.D., Reynoldson, J.A., Thompson, R.C., 1997. Ribosomal RNA sequencing reveals dierences between the genotypes of Giardia isolates recovered from humans and dogs living in the same locality. J. Parasitol. 83, 4451.
ARTICLE IN PRESS
14 L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Lalle, M., Pozio, E., Capelli, G., Bruschi, F., Crotti, D., Caccio, S.M., 2005b. Genetic heterogeneity at the beta-giardin locus among human and animal isolates of Giardia duodenalis and identication of potentially zoonotic subgenotypes. Int. J. Parasitol. 35, 207213. Lalle, M., Frangipane di Regalbono, A., Poppi, L., Nobili, G., Tonanzi, D., Pozio, E., Caccio, S.M., 2007. A novel Giardia duodenalis assemblage A subtype in fallow deer. J. Parasitol. 93, 426428. Langkjaer, R.B., Vigre, H., Enemark, H.L., Maddox-Hyttel, C., 2007. Molecular and phylogenetic characterization of Cryptosporidium and Giardia from pigs and cattle in Denmark. Parasitology 134, 339350. Learmonth, J.J., Ionas, G., Pita, A.B., Cowie, R.S., 2003. Identication and genetic characterisation of Giardia and Cryptosporidium strains in humans and dairy cattle in the Waikato Region of New Zealand. Water Sci. Technol. 47, 2126. Learmonth, J.J., Ionas, G., Ebbett, K.A., Kwan, E.S., 2004. Genetic characterization and transmission cycles of Cryptosporidium species isolated from humans in New Zealand. Appl. Environ. Microbiol. 70, 39733978. Leav, B.A., Mackay, M.R., Anyanwu, A., OConnor, R.M., Cevallos, A.M., Kindra, G., Rollins, N.C., Bennish, M.L., Nelson, R.G., Ward, H.D., 2002. Analysis of sequence diversity at the highly polymorphic Cpgp40/15 locus among Cryptosporidium isolates from human immunodeciency virus-infected children in South Africa. Infect Immun. 70, 38813890. Lebbad, M., Ankarklev, J., Tellez, A., Leiva, B., Andersson, J.O., Svard, S., in press. Dominance of Giardia assemblage B in Leon, Nicaragua. Acta Trop. Lee, J.H., Lee, J., Park, S.J., Yong, T.S., Hwang, U.W., 2006. Detection and genotyping of Giardia intestinalis isolates using intergenic spacers(IGS)-based PCR. Korean J. Parasitol. 44, 343353. Leonhard, S., Pster, K., Beelitz, P., Wielinga, C., Thompson, R.C., 2007. The molecular characterisation of Giardia from dogs in southern Germany. Vet. Parasitol. 150, 3338. Leoni, F., Amar, C., Nichols, G., Pedraza-Diaz, S., McLauchlin, J., 2006. Genetic analysis of Cryptosporidium from 2414 humans with diarrhoea in England between 1985 and 2000. J. Med. Microbiol. 55, 703707. Leoni, F., Mallon, M.E., Smith, H.V., Tait, A., McLauchlin, J., 2007. Multilocus analysis of Cryptosporidium hominis and Cryptosporidium parvum from sporadic and outbreak-related human cases and C. parvum from sporadic cases in livestock in the UK. J. Clin. Microbiol. 45, 32863294. Llorente, M.T., Clavel, A., Goni, M.P., Varea, M., Seral, C., Becerril, R., Suarez, L., Gomez-Lus, R., 2007. Genetic characterization of Cryptosporidium species from humans in Spain. Parasitol. Int. 56, 201205. Lopez, C.E., Dykes, A.C., Juranek, D.D., Sinclair, S.P., Conn, J.M., Christie, R.W., Lippy, E.C., Schultz, M.G., Mires, M.H., 1980. Waterborne giardiasis: a communitywide outbreak of disease and a high rate of asymptomatic infection. Am. J. Epidemiol. 112, 495507. Lu, S., Wen, J., Li, J., Wang, F., 2002. DNA sequence analysis of the triose phosphate isomerase gene from isolates of Giardia lamblia. Chin. Med. J. (Engl.) 115, 99102. Mallon, M., MacLeod, A., Wastling, J., Smith, H., Reilly, B., Tait, A., 2003a. Population structures and the role of genetic exchange in the zoonotic pathogen Cryptosporidium parvum. J. Mol. Evol. 56, 407417. Mallon, M.E., MacLeod, A., Wastling, J.M., Smith, H., Tait, A., 2003b. Multilocus genotyping of Cryptosporidium parvum type 2: population genetics and sub-structuring. Infect. Genet. Evol. 3, 207218. Mathias, R.G., Riben, P.D., Osei, W.D., 1992. Lack of an association between endemic giardiasis and a drinking water source. Can. J. Public Health 83, 382384. Matsubayashi, M., Abe, N., Takami, K., Kimata, I., Iseki, M., Nakanishi, T., Tani, H., Sasai, K., Baba, E., 2004. First record of Cryptosporidium infection in a raccoon dog (Nyctereutes procyonoides viverrinus). Vet. Parasitol. 120, 171175. McCarthy, S., Ng, J., Gordon, C., Miller, R., Wyber, A., Ryan, U.M., 2008. Prevalence of Cryptosporidium and Giardia species in animals in irrigation catchments in the southwest of Australia. Exp. Parasitol. 118, 596599.
Hoque, M.E., Hope, V.T., Kjellstrom, T., Scragg, R., Lay-Yee, R., 2002. Risk of giardiasis in Aucklanders: a case-control study. Int. J. Infect. Dis. 6, 191197. Hoque, M.E., Hope, V.T., Scragg, R., Kjellstrom, T., 2003. Children at risk of giardiasis in Auckland: a case-control analysis. Epidemiol. Infect. 131, 655662. Hsu, B.M., Wun, H.Y., Hsu, P.C., 2007. Prevalence and genotyping of Giardia in husbandry systems in Taiwan. Parasitol. Res. 101, 275280. Huber, F., da Silva, S., Bomm, T.C., Teixeira, K.R., Bello, A.R., 2007. Genotypic characterization and phylogenetic analysis of Cryptosporidium sp. from domestic animals in Brazil. Vet. Parasitol. 150, 6574. Hunt, C.L., Ionas, G., Brown, T.J., 2000. Prevalence and strain dierentiation of Giardia intestinals is in calves in the Manawatu and Waikato regions of North island, New Zealand. Vet. Parasitol. 91, 7 13. Hunter, P.R., Chalmers, R.M., Syed, Q., Hughes, L.S., Woodhouse, S., Swift, L., 2003. Foot and mouth disease and cryptosporidiosis: possible interaction between two emerging infectious diseases. Emerg. Infect. Dis. 9, 109112. Hunter, P.R., Hughes, S., Woodhouse, S., Syed, Q., Verlander, N.Q., Chalmers, R.M., Morgan, K., Nichols, G., Beeching, N., Osborn, K., 2004. Sporadic cryptosporidiosis case-control study with genotyping. Emerg. Infect. Dis. 10, 12411249. Hunter, P.R., Thompson, R.C., 2005. The zoonotic transmission of Giardia and Cryptosporidium. Int. J. Parasitol. 35, 11811190. Hunter, P.R., Hadeld, S.J., Wilkinson, D., Lake, I.R., Harrison, F.C., Chalmers, R.M., 2007. Subtypes of Cryptosporidium parvum in humans and disease risk. Emerg. Infect. Dis. 13, 8288. Inpankaew, T., Traub, R., Thompson, R.C., Sukthana, Y., 2007. Canine parasitic zoonoses in Bangkok temples. Southeast Asian J. Trop. Med. Public Health 38, 247255. Iseki, M., 1979. Cryptosporidium felis sp. n. (Protozoa, Eimeriorina) from the domestic cat. Jpn. J. Parasitol. 28, 285307. Itagaki, T., Kinoshita, S., Aoki, M., Itoh, N., Saeki, H., Sato, N., Uetsuki, J., Izumiyama, S., Yagita, K., Endo, T., 2005. Genotyping of Giardia intestinalis from domestic and wild animals in Japan using glutamete dehydrogenase gene sequencing. Vet. Parasitol. 133, 283287. Jellison, K.L., Distel, D.L., Hemond, H.F., Schauer, D.B., 2004. Phylogenetic analysis of the hypervariable region of the 18S rRNA gene of Cryptosporidium oocysts in feces of Canada geese (Branta canadensis): evidence for ve novel genotypes. Appl. Environ. Microbiol. 70, 452458. Karanis, P., Ey, P.L., 1998. Characterization of axenic isolates of Giardia intestinalis established from humans and animals in Germany. Parasitol. Res. 84, 442449. Katsumata, T., Hosea, D., Wasito, E.B., Kohno, S., Hara, K., Soeparto, P., Ranuh, I.G., 1998. Cryptosporidiosis in Indonesia: a hospital-based study and a community-based survey. Am. J. Trop. Med. Hyg. 59, 628632. Katsumata, T., Hosea, D., Ranuh, I.G., Uga, S., Yanagi, T., Kohno, S., 2000. Short report: possible Cryptosporidium muris infection in humans. Am. J. Trop. Med. Hyg. 62, 7072. Kiang, K.M., Scheftel, J.M., Leano, F.T., Taylor, C.M., Belle-Isle, P.A., Cebelinski, E.A., Danila, R., Smith, K.E., 2006. Recurrent outbreaks of cryptosporidiosis associated with calves among students at an educational farm programme, Minnesota, 2003. Epidemiol. Infect. 134, 878886. Kvac, M., Kouba, M., Vtovec, J., 2006. Age-related and housingdependence of Cryptosporidium infection of calves from dairy and beef herds in South Bohemia, Czech Republic. Vet. Parasitol. 137, 202209. Lake, I.R., Harrison, F.C., Chalmers, R.M., Bentham, G., Nichols, G., Hunter, P.R., Kovats, R.S., Grundy, C., 2007. Case-control study of environmental and social factors inuencing cryptosporidiosis. Eur. J. Epidemiol. 22, 805811. Lalle, M., Jimenez-Cardosa, E., Caccio, S.M., Pozio, E., 2005a. Genotyping of Giardia duodenalis from humans and dogs from Mexico using a beta-giardin nested polymerase chain reaction assay. J. Parasitol. 91, 203205.
ARTICLE IN PRESS
L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx McLauchlin, J., Pedraza-Diaz, S., Amar-Hoetzeneder, C., Nichols, G.L., 1999. Genetic characterization of Cryptosporidium strains from 218 patients with diarrhea diagnosed as having sporadic cryptosporidiosis. J. Clin. Microbiol. 37, 31533158. McLauchlin, J., Amar, C., Pedraza-Diaz, S., Nichols, G.L., 2000. Molecular epidemiological analysis of Cryptosporidium spp. in the UK: results of genotyping Cryptosporidium spp. in 1,705 fecal samples from humans and 105 fecal samples from livestock animals. J. Clin. Microbiol. 38, 39843990. Meamar, A.R., Guyot, K., Certad, G., Dei-Cas, E., Mohraz, M., Mohebali, M., Mohammad, K., Mehbod, A.A., Rezaie, S., Rezaian, M., 2007. Molecular characterization of Cryptosporidium isolates from humans and animals in Iran. Appl. Environ. Microbiol. 73, 10331035. Mendonca, C., Almeida, A., Castro, A., de Lurdes Delgado, M., Soares, S., da Costa, J.M., Canada, N., 2007. Molecular characterization of Cryptosporidium and Giardia isolates from cattle from Portugal. Vet. Parasitol. 147, 4750. Misic, Z., Abe, N., 2006. Subtype analysis of Cryptosporidium parvum isolates from calves on farms around Belgrade, Serbia and Montenegro, using the 60 kDa glycoprotein gene sequences. Parasitology 134, 351358. Mitchell, P., Graham, P., Brieseman, M.A., 1993. Giardiasis in Canterbury: the rst nine months reported cases. N Z Med. J. 106, 350352. Molbak, K., Aaby, P., Hojlyng, N., da Silva, A.P., 1994. Risk factors for Cryptosporidium diarrhea in early childhood: a case-control study from Guinea-Bissau, West Africa. Am. J. Epidemiol. 139, 734740. Monis, P.T., Andrews, R.H., Mayrhofer, G., Mackrill, J., Kulda, J., Isaac-Renton, J.L., Ey, P.L., 1998. Novel lineages of Giardia intestinalis identied by genetic analysis of organisms isolated from dogs in Australia. Parasitology 116, 719. Monis, P.T., Andrews, R.H., Mayrhofer, G., Ey, P.L., 1999. Molecular systematics of the parasitic protozoan Giardia intestinalis. Mol. Biol. Evol. 16, 11351144. Monis, P.T., Andrews, R.H., Mayrhofer, G., Ey, P.L., 2003. Genetic diversity within the morphological species Giardia intestinalis and its relationship to host origin. Infect. Genet. Evol. 3, 2938. Morgan, U.M., Pallant, L., Dwyer, B.W., Forbes, D.A., Rich, G., Thompson, R.C., 1998. Comparison of PCR and microscopy for detection of Cryptosporidium parvum in human fecal specimens: clinical trial. J. Clin. Microbiol. 36, 995998. Morgan, U.M., Sturdee, A.P., Singleton, G., Gomez, M.S., Gracenea, M., Torres, J., Hamilton, S.G., Woodside, D.P., Thompson, R.C.A., 1999. The Cryptosporidium mouse genotype is conserved across geographic areas. J. Clin. Microbiol. 37, 13021305. Morgan, U.M., Xiao, L., Monis, P., Fall, A., Irwin, P.J., Fayer, R., Denholm, K.M., Limor, J., Lal, A., Thompson, R.C., 2000. Cryptosporidium spp. in domestic dogs: the dog genotype. Appl. Environ. Microbiol. 66, 22202223. Morse, T.D., Nichols, R.A., Grimason, A.M., Campbell, B.M., Tembo, K.C., Smith, H.V., 2007. Incidence of cryptosporidiosis species in paediatric patients in Malawi. Epidemiol. Infect. 135, 13071315. Muthusamy, D., Rao, S.S., Ramani, S., Monica, B., Banerjee, I., Abraham, O.C., Mathai, D.C., Primrose, B., Muliyil, J., Wanke, C.A., Ward, H.D., Kang, G., 2006. Multilocus genotyping of Cryptosporidium sp. isolates from human immunodeciency virusinfected individuals in South India. J. Clin. Microbiol. 44, 632634. Navin, T.R., Juranek, D.D., Ford, M., Minedew, D.J., Lippy, E.C., Pollard, R.A., 1985. Case-control study of waterborne giardiasis in Reno, Nevada. Am. J. Epidemiol. 122, 269275. Ng, J., Pavlasek, I., Ryan, U.M., 2006. Identication of novel Cryptosporidium genotypes from avian hosts. Appl. Environ. Microbiol. 72, 75487553. Ngouanesavanh, T., Guyot, K., Certad, G., Fichoux, Y.L., Chartier, C., Verdier, R.-I., Cailliez, J.-C., Camus, D., Dei-Cas, E., Banuls, A.-L., 2006. Cryptosporidium population genetics: evidence of clonality in isolates from France and Haiti. J. Eukaryot. Microbiol. 53, S33S36. Nichols, G.L., Chalmers, R.M., Sopwith, W., Regan, M., Hunter, C.A., Grenfell, P., Harrison, F., Lane, C., 2006. Cryptosporidiosis: 15
a report on the surveillance and epidemiology of Cryptosporidium infection in England and Wales. Drinking Water Directorate Contract Number DWI 70/2/201. Drinking Water Inspectorate, UK, pp. 142. Ong, C.S., Eisler, D.L., Goh, S.H., Tomblin, J., Awad-El-Kariem, F.M., Beard, C.B., Xiao, L., Sulaiman, I., Lal, A., Fyfe, M., King, A., Bowie, W.R., Isaac-Renton, J.L., 1999. Molecular epidemiology of cryptosporidiosis outbreaks and transmission in British Columbia, Canada. Am. J. Trop. Med. Hyg. 61, 6369. Ong, C.S., Eisler, D.L., Alikhani, A., Fung, V.W., Tomblin, J., Bowie, W.R., Isaac-Renton, J.L., 2002. Novel Cryptosporidium genotypes in sporadic cryptosporidiosis cases: rst report of human infections with a cervine genotype. Emerg. Infect. Dis. 8, 263268. Palkovic, L., Marousek, V., 1989. The pathogenicity of Cryptosporidium parvum Tyzzer, 1912 and C. baileyi Current, Upton and Haynes 1986 for chickens. Folia Parasitol. (Praha) 36, 209217. Palmer, C.J., Xiao, L., Terashima, A., Guerra, H., Gotuzzo, E., Saldias, G., Bonilla, J.A., Zhou, L., Lindquist, A., Upton, S.J., 2003. Cryptosporidium muris, a rodent pathogen, recovered from a human in Peru. Emerg. Infect. Dis. 9, 11741176. Papini, R., Cardini, G., Paoletti, B., Giangaspero, A., 2007. Detection of Giardia assemblage A in cats in Florence, Italy. Parasitol. Res. 100, 653656. Pavlasek, I., Ryan, U., 2007. The rst nding of a natural infection of Cryptosporidium muris in a cat. Vet. Parasitol. 144, 349352. Pedraza-Diaz, S., Amar, C., McLauchlin, J., 2000. The identication and characterisation of an unusual genotype of Cryptosporidium from human faeces as Cryptosporidium meleagridis. FEMS Microbiol. Lett. 189, 189194. Peng, M.M., Xiao, L., Freeman, A.R., Arrowood, M.J., Escalante, A.A., Weltman, A.C., Ong, C.S., Mac Kenzie, W.R., Lal, A.A., Beard, C.B., 1997. Genetic polymorphism among Cryptosporidium parvum isolates: evidence of two distinct human transmission cycles. Emerg. Infect. Dis. 3, 567573. Peng, M.M., Matos, O., Gatei, W., Das, P., Stantic-Pavlinic, M., Bern, C., Sulaiman, I.M., Glaberman, S., Lal, A.A., Xiao, L., 2001. A comparison of Cryptosporidium subgenotypes from several geographic regions. J. Eukaryot. Microbiol. 48, 28S31S. Peng, M.M., Meshnick, S.R., Cunlie, N.A., Thindwa, B.D., Hart, C.A., Broadhead, R.L., Xiao, L., 2003a. Molecular epidemiology of cryptosporidiosis in children in Malawi. J. Eukaryot. Microbiol. 50 (Suppl.), 557559. Peng, M.M., Wilson, M.L., Holland, R.E., Meshnick, S.R., Lal, A.A., Xiao, L., 2003b. Genetic diversity of Cryptosporidium spp. in cattle in Michigan: implications for understanding the transmission dynamics. Parasitol. Res. 90, 175180. Perz, J.F., Le Blancq, S.M., 2001. Cryptosporidium parvum infection involving novel genotypes in wildlife from lower New York State. Appl. Environ. Microbiol. 67, 11541162. Pieniazek, N.J., Bornay-Llinares, F.J., Slemenda, S.B., da Silva, A.J., Moura, I.N., Arrowood, M.J., Ditrich, O., Addiss, D.G., 1999. New Cryptosporidium genotypes in HIV-infected persons. Emerg. Infect. Dis. 5, 444449. Plutzer, J., Karanis, P., 2007. Genotype and subtype analyses of Cryptosporidium isolates from cattle in Hungary. Vet. Parasitol. 146, 357362. Ponce-Macotela, M., Martinez-Gordillo, M.N., Bermudez-Cruz, R.M., Salazar-Schettino, P.M., Ortega-Pierres, G., Ey, P.L., 2002. Unusual prevalence of the Giardia intestinalis A-II subtype amongst isolates from humans and domestic animals in Mexico. Int. J. Parasitol. 32, 12011202. Power, M.L., Slade, M.B., Sangster, N.C., Veal, D.A., 2004. Genetic characterisation of Cryptosporidium from a wild population of eastern grey kangaroos Macropus giganteus inhabiting a water catchment. Infect. Genet. Evol. 4, 5967. Preiser, G., Preiser, L., Madeo, L., 2003. An outbreak of cryptosporidiosis among veterinary science students who work with calves. J. Am. Coll. Health 51, 213215.
ARTICLE IN PRESS
16 L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Soba, B., Petrovec, M., Mioc, V., Logar, J., 2006. Molecular characterisation of Cryptosporidium isolates from humans in Slovenia. Clin. Microbiol. Infect. 12, 918921. Sopwith, W., Osborn, K., Chalmers, R., Regan, M., 2005. The changing epidemiology of cryptosporidiosis in North West England. Epidemiol. Infect. 133, 785793. Souza, S.L., Gennari, S.M., Richtzenhain, L.J., Pena, H.F., Funada, M.R., Cortez, A., Gregori, F., Soares, R.M., 2007. Molecular identication of Giardia duodenalis isolates from humans, dogs, cats and cattle from the state of Sao Paulo, Brazil, by sequence analysis of fragments of glutamate dehydrogenase (gdh) coding gene. Vet. Parasitol. 149, 258264. Stantic-Pavlinic, M., Xiao, L., Glaberman, S., Lal, A.A., Orazen, T., RatajVerglez, A., Logar, J., Berce, I., 2003. Cryptosporidiosis associated with animal contacts. Wien. Klin. Wochenschr. 115, 125127. Starkey, S.R., Johnson, A.L., Ziegler, P.E., Mohammed, H.O., 2007. An outbreak of cryptosporidiosis among alpaca crias and their human caregivers. J. Am. Vet. Med. Assoc. 231, 15621567. Stuart, J.M., Orr, H.J., Warburton, F.G., Jeyakanth, S., Pugh, C., Morris, I., Sarangi, J., Nichols, G., 2003. Risk factors for sporadic giardiasis: a case-control study in southwestern England. Emerg. Infect. Dis. 9, 229233. Sulaiman, I.M., Xiao, L., Yang, C., Escalante, L., Moore, A., Beard, C.B., Arrowood, M.J., Lal, A.A., 1998. Dierentiating human from animal isolates of Cryptosporidium parvum. Emerg. Infect. Dis. 4, 681685. Sulaiman, I.M., Fayer, R., Bern, C., Gilman, R.H., Trout, J.M., Schantz, P.M., Das, P., Lal, A.A., Xiao, L., 2003. Triosephosphate isomerase gene characterization and potential zoonotic transmission of Giardia duodenalis. Emerg. Infect. Dis. 9, 14441452. Sulaiman, I.M., Hira, P.R., Zhou, L., Al-Ali, F.M., Al-Shelahi, F.A., Shweiki, H.M., Iqbal, J., Khalid, N., Xiao, L., 2005. Unique endemicity of cryptosporidiosis in children in Kuwait. J. Clin. Microbiol. 43, 28052809. Szenasi, Z., Marton, S., Kucsera, I., Tanczos, B., Horvath, K., Orosz, E., Lukacs, Z., Szeidemann, Z., 2007. Preliminary investigation of the prevalence and genotype distribution of Giardia intestinalis in dogs in Hungary. Parasitol. Res. 101 (Suppl. 1), 145152. Tamer, G.S., Turk, M., Dagci, H., Pektas, B., Guy, E.C., Guruz, A.Y., Uner, A., 2007. The prevalence of cryptosporidiosis in Turkish children, and genotyping of isolates by nested polymerase chain reaction-restriction fragment length polymorphism. Saudi Med. J. 28, 12431246. Thompson, H.P., Dooley, J.S., Kenny, J., McCoy, M., Lowery, C.J., Moore, J.E., Xiao, L., 2007. Genotypes and subtypes of Cryptosporidium spp. in neonatal calves in Northern Ireland. Parasitol. Res. 100, 619624. Thompson, R.C., 2000. Giardiasis as a re-emerging infectious disease and its zoonotic potential. Int. J. Parasitol. 30, 12591267. Thompson, R.C., 2004. The zoonotic signicance and molecular epidemiology of Giardia and giardiasis. Vet. Parasitol. 126, 1535. Tiangtip, R., Jongwutiwes, S., 2002. Molecular analysis of Cryptosporidium species isolated from HIV-infected patients in Thailand. Trop. Med. Int. Health 7, 357364. Traub, R.J., Robertson, I.D., Irwin, P., Mencke, N., Monis, P., Thompson, R.C., 2003. Humans, dogs and parasitic zoonoses-unravelling the relationships in a remote endemic community in northeast India using molecular tools. Parasitol. Res. 90 (Suppl. 3), S156S157. Traub, R.J., Monis, P.T., Robertson, I., Irwin, P., Mencke, N., Thompson, R.C., 2004. Epidemiological and molecular evidence supports the zoonotic transmission of Giardia among humans and dogs living in the same community. Parasitology 128, 253262. Traub, R., Wade, S., Read, C., Thompson, A., Mohammed, H., 2005. Molecular characterization of potentially zoonotic isolates of Giardia duodenalis in horses. Vet. Parasitol. 130, 317321. Trotz-Williams, L.A., Martin, D.S., Gatei, W., Cama, V., Peregrine, A.S., Martin, S.W., Nydam, D.V., Jamieson, F., Xiao, L., 2006. Genotype and subtype analyses of Cryptosporidium isolates from dairy calves and humans in Ontario. Parasitol. Res. 99, 346352.
Probert, C.S.J., Emmett, P.M., Heaton, K.W., 1995. Some determinants of whole-gut transit time: a population-based study. Q. J. Med. 88, 311315. Read, C., Walters, J., Robertson, I.D., Thompson, R.C., 2002. Correlation between genotype of Giardia duodenalis and diarrhoea. Int. J. Parasitol. 32, 229231. Read, C.M., Monis, P.T., Thompson, R.C., 2004. Discrimination of all genotypes of Giardia duodenalis at the glutamate dehydrogenase locus using PCR-RFLP. Infect. Genet. Evol. 4, 125130. Rimhanen-Finne, R., Enemark, H.L., Kolehmainen, J., Toropainen, P., Hanninen, M.L., 2007. Evaluation of immunouorescence microscopy and enzyme-linked immunosorbent assay in detection of Cryptosporidium and Giardia infections in asymptomatic dogs. Vet. Parasitol. 145, 345348. Robertson, B., Sinclair, M.I., Forbes, A.B., Veitch, M., Kirk, M., Cunlie, D., Willis, J., Fairley, C.K., 2002. Case-control studies of sporadic cryptosporidiosis in Melbourne and Adelaide, Australia. Epidemiol. Infect. 128, 419431. Robertson, L.J., Forberg, T., Hermansen, L., Hamnes, I.S., Gjerde, B., 2007. Giardia duodenalis cysts isolated from wild moose and reindeer in norway: genetic characterization by PCR-rp and sequence analysis at two genes. J. Wildl. Dis. 43, 576585. Robinson, R.A., Pugh, R.N., 2002. Dogs, zoonoses and immunosuppression. J. R. Soc. Health 122, 9598. Rosales, M.J., Perez Cordon, G., Sanchez Moreno, M., Marin Sanchez, C., Mascaro, C., 2005. Extracellular like-gregarine stages of Cryptosporidium parvum. Acta Trop. 95, 7478. Roy, S.L., DeLong, S.M., Stenzel, S.A., Shiferaw, B., Roberts, J.M., Khalakdina, A., Marcus, R., Segler, S.D., Shah, D.D., Thomas, S., Vugia, D.J., Zansky, S.M., Dietz, V., Beach, M.J., 2004. Risk factors for sporadic cryptosporidiosis among immunocompetent persons in the USA from 1999 to 2001. J. Clin. Microbiol. 42, 29442951. Ruiz, A., Foronda, P., Gonzalez, J.F., Guedes, A., Abreu-Acosta, N., Molina, J.M., Valladares, B., in press. Occurrence and genotype characterization of Giardia duodenalis in goat kids from the Canary Islands, Spain. Vet. Parasitol. Ryan, U., Xiao, L., Read, C., Zhou, L., Lal, A.A., Pavlasek, I., 2003. Identication of novel Cryptosporidium genotypes from the Czech Republic. Appl. Environ. Microbiol. 69, 43024307. Ryan, U.M., Monis, P., Enemark, H.L., Sulaiman, I., Samarasinghe, B., Read, C., Buddle, R., Roberston, I., Zhou, L., Thompson, R.C., Xiao, L., 2004. Cryptosporidium suis n. sp. (Apicomplexa: Cryptosporidiidae) in pigs (Sus scrofa). J. Parasitol. 90, 769773. Ryan, U.M., Bath, C., Robertson, I., Read, C., Elliot, A., McInnes, L., Traub, R., Besier, B., 2005. Sheep may not be an important zoonotic reservoir for Cryptosporidium and Giardia parasites. Appl. Environ. Microbiol. 71, 49924997. Santin, M., Trout, J.M., Xiao, L., Zhou, L., Greiner, E., Fayer, R., 2004. Prevalence and age-related variation of Cryptosporidium species and genotypes in dairy calves. Vet. Parasitol. 122, 103117. Santin, M., Trout, J.M., Vecino, J.A., Dubey, J.P., Fayer, R., 2006. Cryptosporidium, Giardia and Enterocytozoon bieneusi in cats from Bogota (Colombia) and genotyping of isolates. Vet. Parasitol. 141, 334339. Santin, M., Trout, J.M., Fayer, R., 2007. Prevalence and molecular characterization of Cryptosporidium and Giardia species and genotypes in sheep in Maryland. Vet. Parasitol. 146, 1724. Satoh, M., Matsubara-Nihei, Y., Sasaki, T., Nakai, Y., 2006. Characterization of Cryptosporidium canis isolated in Japan. Parasitol. Res. 99, 746748. Smerdon, W.J., Nichols, T., Chalmers, R.M., Heine, H., Reacher, M.H., 2003. Foot and mouth disease in livestock and reduced cryptosporidiosis in humans, England and wales. Emerg. Infect. Dis. 9, 2228. Smith, K.E., Stenzel, S.A., Bender, J.B., Wagstrom, E., Soderlund, D., Leano, F.T., Taylor, C.M., Belle-Isle, P.A., Danila, R., 2004. Outbreaks of enteric infections caused by multiple pathogens associated with calves at a farm day camp. Pediatr. Infect. Dis. J. 23, 1098 1104.
ARTICLE IN PRESS
L. Xiao, R. Fayer / International Journal for Parasitology xxx (2008) xxxxxx Trout, J.M., Santin, M., Fayer, R., 2003. Identication of assemblage A Giardia in white-tailed deer. J. Parasitol. 89, 12541255. Trout, J.M., Santin, M., Greiner, E., Fayer, R., 2004. Prevalence of Giardia duodenalis genotypes in pre-weaned dairy calves. Vet. Parasitol. 124, 179186. Trout, J.M., Santin, M., Greiner, E., Fayer, R., 2005. Prevalence and genotypes of Giardia duodenalis in post-weaned dairy calves. Vet. Parasitol. 130, 177183. Trout, J.M., Santin, M., Fayer, R., 2006a. Giardia and Cryptosporidium species and genotypes in coyotes (Canis latrans). J. Zoo Wildl. Med. 37, 141144. Trout, J.M., Santin, M., Greiner, E.C., Fayer, R., 2006b. Prevalence and genotypes of Giardia duodenalis in 12 year old dairy cattle. Vet. Parasitol. 140, 217222. Trout, J.M., Santin, M., Fayer, R., 2007. Prevalence of Giardia duodenalis genotypes in adult dairy cows. Vet. Parasitol. 147, 205209. Trout, J.M., Santin, M., Fayer, R., in press. Detection of assemblage A Giardia duodenalis and Eimeria spp. in alpacas on two Maryland farms. Vet. Parasitol. Tumwine, J.K., Kekitiinwa, A., Nabukeera, N., Akiyoshi, D.E., Rich, S.M., Widmer, G., Feng, X., Tzipori, S., 2003. Cryptosporidium parvum in children with diarrhea in Mulago Hospital, Kampala, Uganda. Am. J. Trop. Med. Hyg. 68, 710715. Tumwine, J.K., Kekitiinwa, A., Bakeera-Kitaka, S., Ndeezi, G., Downing, R., Feng, X., Akiyoshi, D.E., Tzipori, S., 2005. Cryptosporidiosis and microsporidiosis in Ugandan children with persistent diarrhea with and without concurrent infection with the human immunodeciency virus. Am. J. Trop. Med. Hyg. 73, 921925. Twomey, D.F., Barlow, A.M., Bell, S., Chalmers, R.M., Elwin, K., Giles, M., Higgins, R.J., Robinson, G., Stringer, R.M., 2008. Cryptosporidiosis in two alpaca (Lama pacos) holdings in the South-West of England. Vet. J. 175, 419422. Uehlinger, F.D., Barkema, H.W., Dixon, B.R., Coklin, T., OHandley, R.M., 2006. Giardia duodenalis and Cryptosporidium spp. in a veterinary college bovine teaching herd. Vet. Parasitol. 142, 231237. van der Giessen, J.W., de Vries, A., Roos, M., Wielinga, P., Kortbeek, L.M., Mank, T.G., 2006. Genotyping of Giardia in Dutch patients and animals: a phylogenetic analysis of human and animal isolates. Int. J. Parasitol. 36, 849858. Vasilopulos, R.J., Rickard, L.G., Mackin, A.J., Pharr, G.T., Huston, C.L., 2007. Genotypic analysis of Giardia duodenalis in domestic cats. J. Vet. Intern. Med./Am. Coll. Vet. Intern. Med. 21, 352355. Volotao, A.C., Costa-Macedo, L.M., Haddad, F.S., Brandao, A., Peralta, J.M., Fernandes, O., 2007. Genotyping of Giardia duodenalis from human and animal samples from Brazil using beta-giardin gene: a phylogenetic analysis. Acta Trop. 102, 1019. Warburton, A.R., Jones, P.H., Bruce, J., 1994. Zoonotic transmission of giardiasis: a case control study. Commun. Dis. Rep. CDR Rev. 4, R32R36. Welch, T.P., 2000. Risk of giardiasis from consumption of wilderness water in North America: a systematic review of epidemiologic data. Int. J. Infect. Dis. 4, 100103. Wielinga, C.M., Thompson, R.C., 2007. Comparative evaluation of Giardia duodenalis sequence data. Parasitology 134, 17951821. 17
Wielinga, P.R., de Vries, A., van der Goot, T.H., Mank, T., Mars, M.H., Kortbeek, L.M., van der Giessen, J.W.B., 2008. Molecular epidemiology of Cryptosporidium in humans and cattle in The Netherlands. Int. J. Parasitol. 38, 809817. Woods, K.M., Upton, S.J., 2007. In vitro development of Cryptosporidium parvum in serum-free media. Lett. Appl. Microbiol. 44, 520523. Wu, Z., Nagano, I., Boonmars, T., Nakada, T., Takahashi, Y., 2003. Intraspecies polymorphism of Cryptosporidium parvum revealed by PCR-restriction fragment length polymorphism (RFLP) and RFLPsingle-strand conformational polymorphism analyses. Appl. Environ. Microbiol. 69, 47204726. Xiao, L., Bern, C., Limor, J., Sulaiman, I., Roberts, J., Checkley, W., Cabrera, L., Gilman, R.H., Lal, A.A., 2001. Identication of 5 types of Cryptosporidium parasites in children in Lima, Peru. J. Infect. Dis. 183, 492497. Xiao, L., Bern, C., Arrowood, M., Sulaiman, I., Zhou, L., Kawai, V., Vivar, A., Lal, A.A., Gilman, R.H., 2002. Identication of the Cryptosporidium pig genotype in a human patient. J. Infect. Dis. 185, 18461848. Xiao, L., Bern, C., Sulaiman, I.M., Lal, A.A., 2004a. Molecular epidemiology of human cryptosporidiosis. In: Thompson, R.C.A., Armson, A., Ryan, U.M. (Eds.), Cryptosporidium: From Molecules to Disease. Elsevier, Amsterdam, pp. 121146. Xiao, L., Fayer, R., Ryan, U., Upton, S.J., 2004b. Cryptosporidium taxonomy: recent advances and implications for public health. Clin. Microbiol. Rev. 17, 7297. Xiao, L., Ryan, U.M., 2004. Cryptosporidiosis: an update in molecular epidemiology. Curr. Opin. Infect. Dis. 17, 483490. Xiao, L., Ryan, U.M., Graczyk, T.K., Limor, J., Li, L., Kombert, M., Junge, R., Sulaiman, I.M., Zhou, L., Arrowood, M.J., Koudela, B., Modry, D., Lal, A.A., 2004c. Genetic diversity of Cryptosporidium spp. in captive reptiles. Appl. Environ. Microbiol. 70, 891 899. Xiao, L., Cama, V.A., Cabrera, L., Ortega, Y., Pearson, J., Gilman, R.H., 2007a. Possible transmission of Cryptosporidium canis among children and a dog in a household. J. Clin. Microbiol. 45, 20142016. Xiao, L., Zhou, L., Santin, M., Yang, W., Fayer, R., 2007b. Distribution of Cryptosporidium parvum subtypes in calves in eastern USA. Parasitol. Res. 100, 701706. Xiao, L., Ryan, U.M., 2008. Molecular epidemiology. In: Fayer, R., Xiao, L. (Eds.), Cryptosporidium and Cryptosporidiosis, second ed. CRC Press and IWA Publishing, Boca Raton, FL, pp. 119163. Yason, J.A., Rivera, W.L., 2007. Genotyping of Giardia duodenalis isolates among residents of slum area in Manila, Philippines. Parasitol. Res. 101, 681687. Yoder, J.S., Beach, M.J., 2007. Cryptosporidiosis surveillance USA, 20032005. MMWR Surveill. Summ. 56, 110. Zhou, L., Fayer, R., Trout, J.M., Ryan, U.M., Schaefer 3rd, F.W., Xiao, L., 2004a. Genotypes of Cryptosporidium species infecting fur-bearing mammals dier from those of species infecting humans. Appl. Environ. Microbiol. 70, 75747577. Zhou, L., Kassa, H., Tischler, M.L., Xiao, L., 2004b. Host-adapted Cryptosporidium spp. in canada geese (Branta canadensis). Appl. Environ. Microbiol. 70, 42114215.

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International Journal for Parasitology xxx (2008) xxxxxx www.elsevier.com/locate/ijpara

Cryptosporidium suis Cryptosporidium varanii Cryptosporidium wrairi

Ryan et al. (2004) Pavlasek et al. (1995) Vetterling et al. (1971)

Cryptosporidium parvum Cryptosporidium suis Cervine genotype

Assemblage B Assemblage Assemblage Assemblage Assemblage Assemblage C D E F G

C (2) and unknown (1)

A+B (1) A4 (probably C or D) (4)

AII at glutamate dehydrogenase locus.

Appeared on one farm briey.

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