JP2001509682A - New Streptococcus ERS - Google Patents

Abstract

  (57) [Summary] Provided are gluS polypeptides and DNA (RNA) encoding the gluS polypeptides, as well as methods for producing such polypeptides by recombinant methods, and methods of using the gluS polypeptides for screening antibacterial compounds.

Description

Description: FIELD OF THE INVENTION The present invention relates to newly identified polynucleotides and polypeptides, and their manufacture and use, as well as their variants, agonists and antagonists, and their uses. In particular, in these and other respects, the present invention relates to novel polynucleotides and polypeptides of the glutamyl-tRNA synthetase family (hereinafter "gluS"). BACKGROUND OF THE INVENTION Streptococci form a medically important microbial genus, and in humans, for example, otitis media, conjunctivitis, pneumonia, bacteremia, meningitis, sinusitis, empyema and endocarditis. It is known to cause several types of disease, most particularly meningitis, such as, for example, cerebrospinal fluid infection. Since more than 100 years have passed since the isolation of the genus Streptococcus, Streptococcus pneumoniae is one of the microorganisms that has been studied in more detail. For example, in fact, much of the early view that DNA is the genetic material was stated in Griffith's and Avery, Macleod and McCarty studies using this microorganism. Despite the vast amount of research on Streptococcus pneumoniae, many questions remain regarding the toxicity of this microorganism. It is particularly preferred to use Streptococcus genes and gene products as targets for the development of antibiotics. The frequency of Streptococcus pneumoniae infections has increased dramatically over the past two decades. This has been attributed to the emergence of multiple antibiotic resistant strains and an increasing population of people with a compromised immune system. It is no longer uncommon to isolate Streptococcus pneumoniae strains that are resistant to some or all of the standard antibiotics. This phenomenon has created a need for new antimicrobial agents, vaccines and diagnostic tests for this organism. The t-RNA synthetase has the important role in protein synthesis shown in the following scheme: Enzyme + ATP + AA⇔Enzyme AA-AMP + PPi Enzyme AA-AMP + t-RNA⇔Enzyme + AMP + AA-t-RNA [where AA means an amino acid] are doing. Inhibition of this process leads to a decrease in charged tRNA levels, which triggers a cascade of responses known as stringent responses, thereby inducing a dormant state of the organism. As such, inhibitors of bacterial t-RNA synthetase have potential as antibacterial agents. One example of such is mupirocin, which is a selective inhibitor of isoleucyl t-RNA synthetase. Other t-RNA synthetases are currently being tested as antibacterial targets, and this process is greatly facilitated by the isolation of synthetases. Clearly, there is a need for factors, such as the novel compounds of the present invention, which have the immediate benefit of being useful for screening compounds for antibiotic activity. Such factors are also useful for examining their role in the development of infection, dysfunction and disease. There is also a need for such factors and their antagonists and agonists that can play a role in preventing, ameliorating or correcting infection, dysfunction or disease. The polypeptides of the invention have amino acid sequence homology to the known Bacillus subtilis glutamyl tRNA synthetase protein. SUMMARY OF THE INVENTION Due to the homology between the amino acid sequence shown in Table 1 (SEQ ID NO: 2) and known amino acid sequences or sequences of other proteins such as the Bacillus subtilis glutamyl tRNA synthetase protein, the polypeptide is a novel gluS polypeptide. It is an object of the present invention to provide an identified polypeptide. It is a further object of the present invention to provide a polynucleotide encoding a gluS polypeptide, in particular a polynucleotide encoding a polypeptide designated herein as gluS. In a particularly preferred embodiment of the invention, the polynucleotide comprises a region encoding a gluS polypeptide comprising the sequence shown in Table 1 (SEQ ID NO: 1), or a variant thereof. In another particularly preferred embodiment of the present invention, there is a novel gluS protein from Streptococcus pneumoniae comprising the amino acid sequence of Table 1 (SEQ ID NO: 2), or a variant thereof. According to another aspect of the present invention, there is provided an isolated nucleic acid molecule encoding a mature polypeptide expressible by Streptococcus pneumoniae strain 0100993, contained in the deposited strain. A further aspect of the present invention provides an isolated nucleic acid molecule encoding gluS, in particular gluS of Streptococcus pneumoniae, including mRNA, cDNA, genomic DNA. Further embodiments of the present invention include biologically, diagnostically, prophylactically, clinically or therapeutically useful variants thereof, and compositions comprising them. According to another aspect of the present invention there is provided the use of a polynucleotide of the present invention for therapeutic or prophylactic purposes, particularly for genetic immunity. Particularly preferred embodiments of the present invention include naturally occurring allelic variants of gluS and the polypeptides encoded thereby. In another aspect of the invention, a novel polypeptide of Streptococcus pneumoniae, referred to herein as gluS, and biologically, diagnostically, prophylactically, clinically or therapeutically useful fragments, variants thereof And derivatives, and variants and derivatives of the above-described fragments and analogs, and compositions comprising them. Particularly preferred embodiments of the invention include variants of the gluS polypeptide encoded by naturally occurring alleles of the gluS gene. In a preferred embodiment of the present invention, there is a method for producing the above-mentioned gluS polypeptide. According to yet another aspect of the present invention, there are provided inhibitors of such polypeptides, including, for example, antibodies, which are useful as antibacterial agents. According to certain preferred embodiments of the present invention, assess gluS expression, treat disease, such as otitis media, conjunctivitis, pneumonia, bacteremia, meningitis, sinusitis, empyema and endocarditis, most particularly Administers gluS polypeptides or polynucleotides to an organism to generate an immunological response to, for example, treatment of meningitis, such as cerebrospinal fluid infection, genetic mutation assays, and bacteria, especially Streptococcus pneumoniae bacteria Products, compositions and methods are provided for doing so. According to certain preferred embodiments of this and other aspects of the invention, there are provided, in particular, polynucleotides that hybridize under stringent conditions to a gluS polynucleotide sequence. In certain preferred embodiments of the present invention, there are provided antibodies against the gluS polypeptide. In another embodiment of the present invention, there is provided a method of identifying a compound that binds to or interacts with a polypeptide or polynucleotide of the present invention to inhibit or activate their activity, the method comprising: The polypeptide or polynucleotide of the present invention is contacted with the compound to be screened under conditions that allow binding or other interaction with the polypeptide or polynucleotide to allow binding or other interaction with the compound. Assessing (such binding or interaction is associated with a second compound capable of providing a detectable signal in response to binding or interaction of the compound with the polypeptide or polynucleotide); Of signals resulting from the binding or interaction of a compound with a polypeptide or polynucleotide Detecting the presence or absence of a compound involves determining whether a compound binds or interacts with a polypeptide or polynucleotide to activate or inhibit their activity. According to yet another aspect of the present invention there are provided gluS agonists and antagonists, preferably bacteriostatic or bactericidal agonists and antagonists. In a further aspect of the present invention, there is provided a composition comprising a gluS polynucleotide or a gluS polypeptide for administration to a unicellular or multicellular organism. Various changes and modifications within the spirit and scope of the disclosed invention will become readily apparent to those skilled in the art from reading the following description and from reading the remainder of the specification. Terminology The following description is provided to facilitate understanding of certain terms that are commonly used herein, particularly in the examples. A “host cell” is a cell that has been transformed or transfected, or is capable of being transformed or transfected by an exogenous polynucleotide sequence. As is well known in the art, "identity" is a relationship between two or more polypeptide sequences or between two or more polynucleotide sequences, as determined by comparing the sequences. is there. In the art, "identity" also sometimes means the degree of relatedness between two polypeptide or polynucleotide sequences, as determined by the match between the two strands of such sequences. "Identity" and "similarity" can both be easily calculated by known methods (Computational Molecular Biology, Less, AM, Oxford University Press, New York, 1988; Biocomputing: Information and Genome Projects, Smith, DW, Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, AM and Griffin, HG, Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G ., Academic Press, 1987; and Sequence Analysis Primer, edited by Gribskov, M. and Devereux, J., M. Stockton Press, New York, 1991; and Carillo, H., and Lipman, D., SIAM. J., Applied Math., 48: 1073 (1988)). Preferred methods for determining identity are designed to give the best match between the two sequences tested. Methods for determining identity and similarity are codified in publicly available computer programs. A preferred computer programming method to determine the identity and similarity of two sequences is the GCG program package (Devereux, J. et al., Nucleic Acids Research 12 (1): 387 (1984), BLASTP, BLASTN and FASTA ( Atschul, SF et al., J. Molec. Biol. 215: 403-410 (1990))). The BLASTX program is publicly available from NCBI and other sources (BLAST Manual, Altschul, S., et al., NCBI NLM NIH Bethesda, MD 20894; Altschul, S., et al., J. Mol. Biol. 215: 403-410 (1990)). As an example, a polynucleotide having a nucleotide sequence having at least 95% identity to a control nucleotide sequence of SEQ ID NO: 1, for example, is a polynucleotide whose nucleotide sequence is the nucleotide of a control nucleotide acid sequence of SEQ ID NO: 1. The nucleotide sequence of the polynucleotide is identical to the control sequence except that it can include up to 5 nucleotide changes for every 100. In other words, to obtain a polypeptide having a nucleotide sequence that is at least 95% identical to the control acid sequence, up to 5% of the nucleotides in the control sequence may be deleted or replaced with another nucleotide. Alternatively, up to 5% of all nucleotides in the control sequence may be inserted into the control sequence. These mutations in the control sequence may be at the 5 'or 3' terminal position of the control nucleotide sequence, or may be at any position between those terminal positions, It may be interspersed with nucleotides, or may be one or more contiguous groups within a control sequence. Similarly, for a polypeptide having an amino acid sequence having at least 95% identity to the control amino acid sequence of SEQ ID NO: 2, for example, the polypeptide sequence may be an amino acid of the control amino acid sequence of SEQ ID NO: 2 The amino acid sequence of the polypeptide is identical to the control sequence, except that it can contain up to 5 amino acid changes for every 100 amino acids. In other words, to obtain a polypeptide having an amino acid sequence that is at least 95% identical to the control amino acid sequence, up to 5% of the amino acids in the control sequence may be deleted or substituted with other amino acids. Alternatively, up to 5% of all amino acids in the control sequence may be inserted into the control sequence. These changes in the control sequence may be at the amino or carboxy terminal position of the control amino acid sequence, or may be at any position between their ends, and may be interspersed in the control sequence. Or one or more contiguous groups within a control sequence. “Isolated” means altered “by the hand of man” from its natural state, ie, in the case of natural products, altered or removed from its original environment, or both. For example, a polynucleotide or polypeptide that is naturally occurring in a living organism is not `` isolated '', but the same polynucleotide or polypeptide separated from its coexisting material in its natural state is a term used herein. Has been "isolated". "Polynucleotide (s)" also generally means a polyribonucleotide or polydeoxyribonucleotide, which may be unmodified RNA or DNA, or modified RNA or DNA. Thus, a "polynucleotide" is a DNA, single-stranded or double-stranded DNA, a mixture of single- and double-stranded regions or a mixture of single-, double- and triple-stranded regions, among others. And double-stranded RNA, and RNA, a mixture of single- and double-stranded regions, single-stranded or more typically double- or triple-stranded, or a mixture of single- and double-stranded regions But not limited to hybrid molecules including DNA and RNA. In addition, "polynucleotide" as used herein refers to triple-stranded regions comprising RNA or DNA or both RNA and DNA. The chains in such regions may be from the same molecule or from different molecules. This region may include all one or more of these molecules, but more typically includes only one region of some of the molecules. One of the molecules of the triple helix region is often an oligonucleotide. As used herein, the term "polynucleotide" includes DNAs or RNAs as described above containing one or more modified bases. Thus, DNA or RNA having a backbone that has been modified for stability or for other reasons is also a "polynucleotide" as contemplated herein. In addition, DNA or RNA containing only unusual bases such as inosine or modified bases such as tritylated bases (only two examples are shown) is also the term polypeptide herein. It will be apparent that numerous modifications have been made to DNA and RNA that serve many useful purposes known to those of skill in the art. The term "polynucleotide", as used herein, refers to such chemically, enzymatically or metabolically modified forms of a polynucleotide, as well as viruses, especially cells, including simple and complex cells. Includes characteristic DNA and RNA chemical forms. "Polynucleotide" embraces short polynucleotides, often referred to as oligonucleotide (s). As used herein, "polypeptide" is used to refer to a peptide or protein containing two or more amino acids linked together linearly by peptide bonds. "Polypeptide" means both short chains, commonly referred to in the art, for example, peptides, oligopeptides and oligomers, and long chains, which come in many forms and are commonly referred to in the art as proteins. Polypeptides may contain amino acids other than the 20 gene-encoded amino acids. "Polypeptide" encompasses natural processes such as processing and other post-translational modifications, as well as by chemical modifications. Such modifications are well described in basic texts and in more detailed articles as well as in numerous research literatures, which are well known to those skilled in the art. It will be appreciated that the same type of modification may be present at the same or varying degrees at several sites in the polypeptide. Modifications can be anywhere in the polypeptide, including the peptide backbone, amino acid side chains, and amino or carboxy termini. Modifications include, for example, acetylation, acylation, ADP-ribosylation, amidation, covalent bonding of flavin, covalent bonding of heme moieties, covalent bonding of nucleotides or nucleotide derivatives, covalent bonding of lipids or lipid derivatives, phosphotidyl Inositol covalent, cross-link, cyclization, disulfide bond formation, demethylation, covalent cross-link formation, cystine formation, pyroglutamate formation, formylation, gamma-carboxylation, sugar chain formation, GPI anchor formation, hydroxylation Transfer RNA-mediated addition of amino acids to proteins, such as, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, arginylation, and ubiquitination There is. For example, it is described in Proteins-Structure and Molecular Properties, 2nd edition, TECreighton, WH Freeman and Company, New York (1993). For example, Posttranslational Covalent Modification of Proteins, edited by BC Johnson, Academic Press, New York (1983), Wold, F., Posttranslational Protein Modifications: Perspective and Prospects, pp. 1-12; Seifter et al., Meth. Enzymol. 182: 626-646 (1990) and Rattan et al., Protein Synthesis: Posttranslational Modifications and Aging, Ann. N. Y. Acad. Sci. 66 3: 48-62 (1992). The polypeptide may be branched or cyclic, with or without branching. Cyclic, branched, and branched and cyclic polypeptides may result from post-translation natural processes, as well as may be produced by entirely synthetic methods. The term "variant" as used herein is a polynucleotide or polypeptide that differs from a reference polynucleotide or polypeptide, respectively, but retains essential properties. A typical variant of a polynucleotide differs in nucleotide sequence from another, reference polynucleotide. Changes in the nucleotide sequence of the variant may or may not change the amino acid sequence of the polypeptide encoded by the control polynucleotide. As discussed below, nucleotide changes result in amino acid substitutions, additions, deletions, fusions and truncations in the polypeptide encoded by the reference sequence. A typical variant of a polypeptide differs in amino acid sequence from another, reference polypeptide. Generally, differences are limited so that the sequences of the control polypeptide and the variant are closely similar overall and, in many regions, identical. Variant and control polypeptides can have an altered amino acid sequence by one or more substitutions, additions, deletions occurring in any combination. The substituted or inserted amino acid residue may or may not be one encoded by the genetic code. A variant of a polynucleotide or polypeptide may be naturally occurring, for example, an allelic variant, or may be a variant that is not known to occur naturally. Non-naturally occurring variants of polynucleotides and polypeptides can be made by mutagenesis techniques or direct synthesis, and other recombinant methods known to those of skill in the art. DESCRIPTION OF THE INVENTION The present invention relates to novel gluS polypeptides and polynucleotides, as described in greater detail below. In particular, the invention relates to novel gluS polypeptides and polynucleotides of Streptococcus pneumoniae, which are related by amino acid sequence homology to Bacillus subtilis glutamyl tRNA synthetase polypeptide. In particular, the present invention relates to gluS having the nucleotide and amino acid sequences shown in Table 1 (SEQ ID NO: 1) and Table 1 (SEQ ID NO: 2), respectively, and furthermore, the gluS nucleotide sequence of the DNA in the strain of the present invention and its coding The amino acid sequence to be determined. Table 1 gluS polynucleotide and polypeptide sequences (A) Streptococcus pneumoniae gluS polynucleotide sequence [SEQ ID NO: 1]. (B) gluS polypeptide sequence [SEQ ID NO: 2] deduced from the polynucleotide sequences in this table. (C) Specific example of polynucleotide sequence [SEQ ID NO: 1]. (D) Specific example of polypeptide sequence [SEQ ID NO: 2]. Deposited Materials The deposited material containing Streptococcus pneumoniae strain 0100993 was found in the National Collection of Industrial and Marine Bacteria Limited (NCIMB), 23 Street, McDrough Drive, Aberdeen AB21RY, Scotland, April 1996. And deposited with NCIMB accession number 40794. After the deposit, the deposited strain is referred to as Streptococcus pneumoniae 0100993 strain. On April 17, 1996, the Streptococcus pneumoniae 0100993 DNA library in E. coli was similarly deposited with the NCIMB and was assigned accession number 40800. The S. pneumoniae strain deposit is referred to herein as the "deposited strain" or "DNA of the deposited strain." The deposited strain contains a full-length response regulator gene. The polynucleotide sequence contained in the deposited strain, as well as the amino acid sequence of the polypeptide encoded thereby, will dominate in events that conflict with any description of the sequences herein. Deposits of the deposited strains have been made under the terms of the Budapest Treaty on the International Recognition of Microbial Deposits for Patent Procedure. When the patent is issued, the shares are eventually sold without any restrictions or conditions. The deposit is provided solely for the convenience of those skilled in the art and does not acknowledge that the deposit is a feasible requirement, as required under 35 USC 112. A license is required to make, use, or sell the deposit, but no such license is granted. Polypeptides The polypeptides of the present invention include the polypeptides of Table 1 [SEQ ID NO: 2] (specifically, mature polypeptides) and polypeptides and fragments, particularly those having the biological activity of gluS, Polypeptides and fragments having at least 70% identity to the polypeptide of Table 1 [SEQ ID NO: 2] or a significant portion thereof, preferably at least 80% to the polypeptide of Table 1 [SEQ ID NO: 2] , More preferably at least 90% similarity (more preferably at least 90% identity) to the polypeptides of Table 1 [SEQ ID NO: 2], even more preferably Table 1 [ SEQ ID NO: 2] has at least 95% similarity (even more preferably at least 95% identity to the polypeptide of SEQ ID NO: 2) The a) polypeptides and fragments, even at least 30 usually, more preferably includes portions of such polypeptides comprising at least 50 amino acids. The invention also includes polypeptides of the formula shown in Table 1 (D), wherein X is hydrogen at the amino terminus, Y is hydrogen or metal at the carboxyl terminus, and R ₁ And R _Two Is an amino acid residue, m is an integer of 1 to 1000 or zero, and n is an integer of 1 to 1000 or zero. The stretch of amino acid residues represented by any of the R groups (where R is greater than one) may be a heteropolymer or a homopolymer, and is preferably a heteropolymer. Other preferred embodiments provide a polypeptide wherein n is zero and m is an integer 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In such preferred embodiments, it is most preferred that the amino terminal amino acid residue is a methionyl residue. Fragments are variant polypeptides that have an amino acid sequence that is entirely identical to some, but not all, of the amino acid sequences of the aforementioned polypeptides. For gluS polypeptides, the fragments may be "free standing" or may be included within a larger polypeptide by forming a part or region, most preferably a single polypeptide. As a large single polypeptide. Preferred fragments include truncated polypeptides having a portion of the amino acid sequence of Table 1 [SEQ ID NO: 2], or variants thereof, including truncating a series of residues including the amino terminus, Or truncated series of residues including the carboxyl terminus. Also preferred are degradation forms of the polypeptides of the present invention in a host, especially Streptococcus pneumoniae. Also, fragments characterized by structural or functional attributes, such as alpha helices and alpha helix forming regions, beta sheets and beta sheet forming regions, turns and turn forming regions, coils and coil forming regions, hydrophilic regions, hydrophobic Also preferred are a region, an alpha-amphiphilic region, a beta amphipathic region, a variable region, a surface-forming region, a substrate-binding region, and a fragment containing a high antigenic index region. Also preferred are biologically active fragments which are those that mediate or improve gluS activity and have reduced undesirable activity. Also included are fragments that are antigenic or immunogenic in animals, especially humans. Fragments containing a receptor or domain of an enzyme that confers a function essential for the survival of Streptococcus pneumoniae in an individual, especially a human, or the ability to initiate or maintain a disease, are particularly preferred. Variants that are fragments of the polypeptides of the present invention may be used for the production of corresponding full-length polypeptides by peptide synthesis, and thus these variants may be used as intermediates for producing full-length polypeptides. A variant that is a fragment of a polynucleotide of the invention may be used to synthesize a full-length polynucleotide of the invention. Polynucleotides Another aspect of the present invention relates to isolated polynucleotides, including the full length gene encoding a gluS polypeptide having the deduced amino acid sequence of Table 1 [SEQ ID NO: 2] and closely related polynucleotides And their variants. Using the information provided herein, for example, to clone and sequence a chromosomal DNA fragment from the starting material Streptococcus pneumoniae 010 0993, using the polynucleotide sequence shown in Table 1 [SEQ ID NO: 1] Standard cloning and screening as used may be used to obtain a polynucleotide of the invention encoding a gluS polypeptide, and then to obtain a full-length clone. For example, the chromosome of Streptococcus pneumoniae 010993 in E. coli or some other suitable host to obtain a polynucleotide sequence of the invention, eg, the sequence shown in Table 1 [SEQ ID NO: 1]. A typical library of clones of DNA is probed with a radiolabeled oligonucleotide, preferably 17-mer or longer, derived from the partial sequence. Clones carrying DNA identical to the probe DNA can be distinguished using stringent conditions. By sequencing the individual clones thus identified using sequencing primers designed from the original sequence, the sequence can be extended in both directions and the entire gene sequence determined. Such sequencing is conveniently performed using denatured double-stranded DNA prepared from a plasmid clone. Suitable techniques are described in Maniatis, T., Fitsch, FF and Sambrook et al., Molecular Cloning, A Laboratory Manual, Second Edition; Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York (1989). (See Screening By Hybridization 1.90 and Sequencing Denatured Double-Stranded DNA Templates 13.70). In a typical example of the present invention, the polynucleotide shown in Table 1 [SEQ ID NO: 1] was found in a DNA library derived from Streptococcus pneumoniae 0100993. The stop codons of the polynucleotide sequences in Table 1 (A) are underlined. The DNA sequence shown in Table 1 [SEQ ID NO: 1] contains an open reading frame encoding a protein having substantially the same number of amino acid residues as the number of amino acid residues shown in Table 1 [SEQ ID NO: 2]. The molecular weight can be calculated using the molecular weight of an amino acid well known in the art. The gluS of the present invention is structurally related to other proteins of the glutamyl tRNA synthetase family, as shown by the results of DNA sequencing. The protein of the present invention exhibits the greatest homology to the Bacillus subtilis glutamyl tRNA synthetase protein among known proteins. The present invention provides a polynucleotide sequence that is identical over its entire length to the coding sequence in Table 1 [SEQ ID NO: 1]. The coding sequence of the mature polypeptide or fragments thereof, as well as the coding sequence of the mature polypeptide in reading frame with other coding sequences or fragments thereof, such as sequences encoding leader or secretory sequences, pre, pro, preproprotein sequences Provided by the present invention. Polynucleotides include, for example, transcribed untranslated sequences, termination signals, ribosome binding sites, sequences that stabilize mRNA, introns, transcribed untranslated sequences such as polyadenylation signals, and additional coding sequences that encode additional amino acids. It may also contain non-coding sequences such as, but not limited to, non-coding 5 'and 3' sequences. For example, it may encode a marker sequence that facilitates purification of the fusion polypeptide. In one preferred embodiment of the invention, the marker sequence is a hexa-histidine peptide (Gentz et al., Proc. Natl. Acad. Sci., USA, 86: 821-) as provided in a pQE vector (Qiagen, Inc.). 824 (1989)) or the HA tag (Wilson et al., Cell, 37: 767 (1984)). The polynucleotides of the present invention also include, but are not limited to, structural genes and native sequences that regulate gene expression. A preferred embodiment of the present invention is a polynucleotide encoding the gluS polypeptide, comprising the nucleotide sequence shown in SEQ ID NO: 1 of Table 1. The invention also encompasses polynucleotides of the formula shown in Table 1 (C), wherein X is hydrogen at the 5 'end, Y is hydrogen or metal at the 3' end, ₁ And R _Two Is a nucleic acid residue, m is an integer of 1 to 1000 or zero, and n is an integer of 1 to 1000 or zero. The extended portion of the nucleic acid residue represented by any of the R groups (m and / or n is an integer greater than 1) may be a heteropolymer or a homopolymer, and is preferably a heteropolymer. Other preferred embodiments provide a polynucleotide wherein n is zero and m is an integer 3, 6, 9, 12, 15, 18, 21, 24, 27, or 30. In such preferred embodiments, it is most preferred that the 5 'terminal nucleic acid residue is ATG or GTG or encodes methionine. The term "polynucleotide encoding a polypeptide" as described herein above includes a polynucleotide comprising a sequence encoding a polypeptide sequence of the present invention, and in particular, a bacterial polypeptide, more particularly A polynucleotide comprising a sequence encoding a glutS polypeptide of Streptococcus pneumoniae having the amino acid sequence shown in Table 1 [SEQ ID NO: 2] is included. The term refers to a single contiguous or discontinuous region encoding a polypeptide (eg, an integrated phage or sequence of phage or sequence), with additional regions that may include coding and / or non-coding sequences. (Interrupted by insertion or editing of the sequence). Furthermore, the present invention also relates to variants of the above polynucleotide that encode variants of the polypeptide having the deduced amino acid sequence of Table 1 [SEQ ID NO: 2]. A variant that is a fragment of a polynucleotide of the invention may be used to synthesize a full-length polynucleotide of the invention. A more particularly preferred embodiment is a polynucleotide encoding a lys variant having the amino acid sequence of the gluS polypeptide of Table 1 [SEQ ID NO: 2], wherein some, a few, 5-10, 5 to 1, 1 to 3, 2, 1 or 0 amino acid residues in any combination of substitution, deletion or addition. Especially preferred among these are silent substitutions, additions and deletions, that do not alter the properties and activities of gluS. A further preferred embodiment of the present invention is a polynucleotide having at least 70% identity over its entire length to a polynucleotide encoding a gluS polypeptide having the amino acid sequence shown in Table 1 [SEQ ID NO: 2]. , And polynucleotides complementary to such polynucleotides. Alternatively, most highly preferred are polynucleotides comprising a region that is at least 80% identical over its entire length to the gluS polynucleotide of a strain of the invention, and polynucleotides complementary thereto. In this regard, polynucleotides that are at least 90% identical over their entire length are particularly preferred, particularly those with at least 95% identity, and even more at least 97% among those with at least 95% identity. It is more preferred, especially at least 98% and at least 99%, even more preferably at least 99%. A particularly preferred embodiment is a polynucleotide that encodes a polypeptide that retains substantially the same biological function or activity as the mature polypeptide encoded by the DNA in Table 1 [SEQ ID NO: 1]. The invention further relates to polynucleotides that hybridize to the sequences described herein above. In this regard, the present invention particularly relates to polynucleotides that hybridize under stringent conditions to the herein above-described polynucleotides. As used herein, the terms "stringent conditions" and "stringent hybridization conditions" refer to hybridizations that occur only when the identity between sequences is at least 95%, preferably at least 97%. An example of stringent hybridization conditions is 50% formamide. In a solution containing 5 × SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5 × Den Hearts solution, 10% dextran sulfate, and 20 μg / ml denatured, sheared salmon sperm DNA , 42 ° C overnight, followed by washing the filters in 0.1 x SSC at about 65 ° C. Hybridization and washing conditions are well known and are illustrated in Sambrook et al., Molecular Cloning, A Laboratory Manual, 2nd edition; Cold Spring Harbor, New York (1989), especially Chapter 11 thereof. The present invention also provides, under stringent hybridization conditions, a suitable library containing the complete gene for the polynucleotide sequence set forth in SEQ ID NO: 1, a probe having the sequence of the polynucleotide sequence set forth in SEQ ID NO: 1 or a fragment thereof. Also provided is a polynucleotide essentially comprising the polynucleotide sequence obtainable by screening and isolating the DNA sequence. Fragments useful for obtaining such polynucleotides include, for example, probes and primers described elsewhere herein. As discussed further herein with respect to the polynucleotide assays of the invention, for example, the polynucleotides of the invention described above may be used to isolate full length cDNA and genomic clones encoding gluS and have a high degree of sequence similarity to the gluS gene. It can be used as a hybridization probe for RNA, cDNA and genomic DNA to isolate cDNA and genomic clones of other genes. Such probes usually contain at least 15 bases. Preferably such probes have at least 30 bases and may have at least 50 bases. Particularly preferred probes have at least 30 bases and are 50 bases or less. For example, the coding region of the gluS gene can be isolated by screening by synthesizing an oligonucleotide probe using the DNA sequence shown in SEQ ID NO: 1. The labeled oligonucleotide having a sequence complementary to the sequence of the gene of the present invention is then used to screen a library of cDNA, genomic DNA or mRNA to determine to which member of the library the probe will hybridize. . The polynucleotides and polypeptides of the present invention can be used, for example, as research reagents and materials for the discovery of therapeutics and diagnostics for diseases, especially human diseases, and are discussed further herein, particularly in relation to polynucleotide assays. . The polynucleotides of the present invention, which are oligonucleotides derived from the sequences of SEQ ID NOs: 1 and / or 2, may be used in the methods described herein, but are preferably used in PCR to identify the polynucleotides identified herein. Determine whether all or part of the nucleotide is transcribed into the infected tissue. It is understood that such sequences are also useful in diagnosing the stage and type of infection achieved by the pathogen. The invention also provides polynucleotides capable of encoding a polypeptide that is a mature protein with additional amino or carboxyl terminal amino acids, or amino acids present in the mature polypeptide (e.g., one or more polypeptide chains in a mature form. If you have). Such sequences play a role in the processing of the protein from the precursor to the mature form, allowing for the transport of the protein, extending or shortening the half-life of the protein, or otherwise manipulating the protein for assay or production. Can be easier. Generally, in vivo, additional amino acids are processed by cellular enzymes and removed from the mature protein. A precursor protein having the mature form of the polypeptide fused to one or more prosequences can be an inactive form of the polypeptide. Removal of the prosequence usually activates such inactive precursors. Some or all of the prosequence can be removed prior to activation. Generally, such precursors are called proproteins. In short, the polynucleotide of the present invention is a mature protein, a mature protein to which a leader sequence is added (also referred to as a preprotein), a precursor of a mature protein having one or more prosequences which are not the leader sequence of the preprotein, Alternatively, it may encode a preproprotein that is a precursor of a proprotein having a leader sequence and one or more prosequences, which are usually removed during a processing step that produces an active and mature form of the polypeptide. . Vectors, Host Cells, Expression The present invention also relates to polynucleotides or vectors containing the polynucleotides of the present invention, host cells that are genetically engineered with vectors of the present invention, and the production of polypeptides of the present invention by recombinant techniques. Using RNA derived from the DNA construct of the present invention, such a protein can be produced using a cell-free translation system. To produce a recombinant, the host cell can be genetically engineered to incorporate an expression system or a portion thereof, or a polynucleotide of the present invention. Introduction of polynucleotides into host cells is described, for example, in Davis et al., Basic Methods in Molecular Biology (1986); Sambrook et al., Molecular Cloning; A Laboratory Manual, Second Edition; Cold Spring Harbor Laboratory Press, Cold Press. Can be performed by methods described in many standard laboratory manuals, such as Spring Harbor, New York (1989), for example, calcium phosphate transfection, DEAE-dextran mediated transfection, transvection, microinjection, positive injection. There are ionic lipid mediated transfection, electroporation, transduction, scrape loading, ballistic transduction and infection and the like. Representative of suitable hosts include bacterial cells, such as Streptococci, Staphylococci, Enterococci, E. coli, Streptomyces. And Bacillus subtiis cells; fungal cells, such as yeast cells and Aspergillus cells; insect cells, such as Drosophila S2 and Spodoptera Sf9 cells; animal cells, such as CHO, COS HeLa, C127, 3T3, BHK, 293 and Bows melanoma cells; and plant cells. Numerous expression systems can be used to produce the polypeptides of the present invention. Such vectors include chromosomal, episomal and viral derived vectors, such as bacterial plasmid derived, bacteriophage derived, transposon derived, yeast episomal derived, insertion element derived, yeast chromosomal element derived such as baculovirus, papovavirus such as SV40, Vectors derived from viruses such as vaccinia virus, adenovirus, fowlpox virus, pseudorabies virus and retrovirus, and vectors derived from combinations thereof, such as vectors derived from genetic elements of plasmids and bacteriophages, such as cosmids And phagemids. The expression system constructs may contain regulatory regions that control and cause expression. In this regard, in general, any system or vector suitable for holding, extending or expressing a polynucleotide in a host and / or expressing a polypeptide can be used for expression. Appropriate DNA sequences may be inserted into the expression system by any of a variety of well-known and conventional techniques, and are described, for example, in Sambrook et al., Molecular Cloning, A Laboratory Manual (supra). The translated protein can be incorporated into a polypeptide that expresses a suitable secretion signal for secretion into the endoplasmic reticulum lumen, periplasmic space or extracellular environment. These signals may be native to the polypeptide or they may be heterologous signals. The polypeptides of the present invention can be recovered and purified from recombinant cell culture by well-known methods, including, for example, ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, Examples include hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography, and lectin chromatography. Most preferably, high performance liquid chromatography is used for purification. If the polypeptide is denatured during isolation and / or purification, well-known techniques for protein regeneration can be used to regain an active conformation. Diagnostic Assays The present invention also relates to the use of a guS polynucleotide of the present invention for use as a diagnostic reagent. Detection of gluS in a eukaryote, particularly a mammal, and especially a human, will provide a diagnostic method for diagnosis of a disease. Eukaryotes (also referred to herein as "individuals"), particularly mammals, and especially humans, infected with an organism containing the gluS gene can be detected at the DNA level by various methods. Diagnostic nucleic acids can be obtained from cells and tissues of infected individuals, such as bone, blood, muscle, cartilage and skin. Genomic DNA may be used directly for detection, or may be amplified enzymatically by using PCR or other amplification methods prior to analysis. RNA or cDNA can also be used in the same way. Using amplification methods, prokaryotic strains present in eukaryotes, particularly mammals, and especially humans, can be characterized by genotyping prokaryotic genes. Deletions and insertions can be detected by a change in size of the amplification product when compared to the genotype of the control sequence. Point mutations can be identified by hybridizing the amplified DNA to a labeled gluS polynucleotide sequence. Perfectly matched sequences can be distinguished from mismatched duplexes by RNase digestion or by differences in melting temperatures. DNA sequence differences may be detected by detecting changes in electrophoretic mobility of DNA fragments in gels with or without denaturing agents, or by direct DNA sequencing. See, for example, Meyers et al., Science, 230: 1242 (1985). Sequence changes at specific locations may also be revealed by nuclease protection assays, such as RNase and S1 protection or chemical cleavage. See, for example, cotton et al., Proc. Natl. Acad. Sci., USA, 85: 4397-4401 (1985). Cells carrying mutations or polymorphisms in the gene of the invention may be detected at the DNA level by various techniques, for example by serotyping. For example, mutations can be detected using RT-PCR. It is particularly preferred to use RT-PCR in combination with an automatic detection system, such as GeneScan. RNA or cDNA may be used for PCR or RT-PCR for the same purpose. By way of example, PCR primers complementary to the nucleic acid encoding gluS can be used to identify and analyze mutations. Further, the present invention provides primers obtained by removing 1, 2, 3 or 4 nucleotides from the 5 'and / or 3' end of these primers. These primers may be used to, among other things, amplify gluS DNA isolated from a sample from an individual. These primers may be used to amplify a gene isolated from an infected individual, and then subject the gene to various techniques for examining DNA sequences. In this way, mutations in the DNA sequence can be detected and used to diagnose infection and serotype and / or classify infectious agents. The invention also relates to diseases, preferably bacterial infections, more preferably infections by Streptococcus pneumoniae, and most preferably otitis media, conjunctivitis, pneumonia, bacteremia, meningitis, sinusitis, empyema and endocarditis. And, most particularly, a method of diagnosing a disease such as meningitis, such as an infection of the cerebrospinal fluid, which comprises measuring the expression level of a polynucleotide having the sequence of Table 1 [SEQ ID NO: 1]. The increase is detected from a sample derived from an individual. Increasing or decreasing the expression of gluS polynucleotides can be determined by any method known in the art for quantifying polynucleotides, such as amplification, PCR, RT-PCR, RNase protection, Northern blotting and other hybridization methods. Can be measured. In addition, the diagnostic assays of the invention for detecting overexpression of gluS protein relative to normal control tissue samples may be used to detect, for example, the presence of an infection. Assay techniques that can be used to determine levels of gluS protein, in a sample derived from a host are well-known to those of skill in the art. Such assays include radioimmunoassays, competitive binding assays, Western blot analysis and ELISA assays. Antibodies Antibodies immunospecific for such polypeptides can be obtained using the polypeptides of the present invention or variants thereof, or cells expressing them, as an immunogen. As used herein, “antibody” includes monoclonal and polyclonal antibodies, chimeras, single chains, monkey and humanized antibodies, and Fab fragments, as well as Fab fragments, such as the products of an immunoglobulin expression library. Included. Antibodies raised against the polypeptides of the invention can be obtained by administering fragments, analogs or cells bearing the polypeptides or epitopes, preferably to non-human animals, using conventional laboratory methods. Monoclonal antibodies can be prepared using techniques well known to those skilled in the art, which provide antibodies produced by continuous cell line cultures. Examples include Kohler, G. and Milstein, C., Nature, 256: 495-497 (1975); Kozbor et al., Immunology Today, 4:72 (1983); Col et al., Monoclonal Antibodies and Cancer Therapy, Alan. There are various techniques as described in R Liss, Inc., pp. 77-96 (1985). Techniques described for the production of single-chain antibodies (US Pat. No. 4,946,778) can be applied to obtain single-chain antibodies to the polypeptides of the invention. In addition, antibodies such as humanized antibodies may be expressed using transgenic mice or other organisms, for example, other mammals. Alternatively, from phage display technology, from a repertoire of PCR-amplified v genes of human lymphocytes screened for having anti-polypeptide, from humans screened for having anti-gluS, Alternatively, an antibody gene having a polypeptide-binding activity can be selected from an untreated library (McCafferty, J. et al., Nature 348: 552-554 (1990); Marks, J. et al., Biotechnology 10: 779). -783 (1992)). The affinity of these antibodies can also be improved by chain shuffling (Clackson, T. et al., Nature 352: 624-628 (1991)). If there are two antigen binding domains, each domain is directed against a different epitope, termed a "bispecific" antibody. Clones expressing the polypeptide may be isolated or identified using the above antibodies, and the antibodies may be purified by affinity chromatography. Thus, in particular, antibodies against gluS are used to infect infections, especially bacterial infections, especially otitis media, conjunctivitis, pneumonia, bacteremia, meningitis, sinusitis, empyema and endocarditis, most particularly, for example, cerebrospinal fluid infection It may be used for treating diseases such as meningitis. Polypeptide variants include antigenically, epitopically or immunologically equivalent variants, and are particular embodiments of the present invention. As used herein, the term "antigenically equivalent derivative" refers to a specific product that, when formed on a protein or polypeptide in accordance with the present invention, interferes with the immediate physical interaction between a pathogen and a mammalian host. Or equivalents thereof that are specifically recognized by the above antibodies. As used herein, the term "immunologically equivalent derivative" refers to an antibody that, when used in a formulation suitable for producing antibodies in vertebrates, causes immediate physical contact between the pathogen and the mammalian host. Includes peptides or equivalents that act to interfere with the interaction. Polypeptides, such as antigenically, immunologically equivalent derivatives, or fusion proteins thereof, can be used as antigens to immunize mice or other animals, such as rats or chickens. Fusion proteins can confer stability on a polypeptide. The antigen can bind to an immunogenic carrier protein, such as by conjugation, such as bovine serum albumin (BSA) or keyhole limp et haemocyanin (KLH). Alternatively, multi-antigen peptides containing multiple copies of the protein or polypeptide, or polypeptides that are antigenically or immunologically equivalent thereto, have sufficient antigenicity to improve immunogenicity. No need to use carrier. Preferably, the antibodies or variants thereof are modified to reduce immunogenicity in the individual. For example, if the individual is a human, most preferably, the antibody is "humanized"; in this case, the complementarity-determining regions of the antibody from the hybridoma have been transplanted into human monoclonal antibodies, e.g., Jones, P. Et al., Nature 321: 522-525 (1986) or Tempest et al., Biotechnology 9: 266-273 (1991). When the polynucleotide of the present invention is used in genetic immunization, for example, direct injection of plasmid DNA into muscle (Wolff et al., Hum. Mol. Genet. 1: 363 (1992); Manthorpe et al., Hum. Gene Ther. 4: 419 (1963)), delivery of complexes of specific protein carriers with DNA (Wu et al., J. Biol. Chem. 264: 16985 (1989)), DNA co-precipitation with calcium phosphate (Benvenisty & Reshef, PNAS). 83: 9551 (1986)), DNA encapsulation in various forms of liposomes (Kaneda et al., Science 243: 375 (1989)), particle bombardment (Tang et al., Nature 356: 152 (1992); Eisenbraun et al., DNA Cell). Biol. 12: 791 (1993)) and in vivo infection with cloned retroviral vectors (Seeger et al., PNAS 81: 5849 (1984)). Antagonists and Agonists-Assays and Molecules The polypeptides of the invention may be used to evaluate the binding of small molecule substrates and ligands, for example, in cells, cell-free preparations, chemical libraries, and natural product mixtures. These substrates and ligands can be natural substrates and ligands, and can be structural or functional mimetics. See, for example, Coligan et al., Current Protocols in Imnlunology 1 (2): Chapter 5 (1991). The present invention also provides a method of screening a compound to identify (agonist) or inhibit (antagonist) the action of a gluS polypeptide or polynucleotide, in particular, a bacteriostatic and / or bactericidal compound. Also provide. The screening method is a high throughput method. For example, to screen for agonists or antagonists, a synthetic reaction mixture, a membrane compartment, a cell compartment such as a cell envelope or cell wall, or a formulation thereof, comprising a gluS polypeptide and a labeled substrate or ligand of such a polypeptide may be expressed as a gluS gonist. Alternatively, the incubation is performed in the absence or presence of a candidate compound that may be an antagonist. The ability of a candidate molecule to agonize or antagonize a gluS polypeptide is reflected in reduced binding of a labeled ligand or reduced production of a product from such a substrate. Molecules that bind and have no effect, ie, that do not induce the effects of gluS, may be the best antagonists. Molecules that bind well and increase the rate of product formation from the substrate are agonists. The production rate or level of product from the substrate can be enhanced by using a reporter system. Reporter systems useful in this regard include colorimetrically labeled substrates that are converted to products, reporter genes that respond to changes in gluS polynucleotide or polypeptide activity, and binding assays that are well known in the art. However, the present invention is not limited to these. Another example of an assay for gluS antagonists is a competition assay in which, under conditions suitable for a competition inhibition assay, gluS and potential antagonists are converted to a gluS binding molecule, a recombinant gluS binding molecule, a natural substrate or ligand, or a substrate. Alternatively, mix with the ligand mimetic. GluS can be labeled, for example, with a radioactive or colorimetric compound, and the number of gluS molecules bound to the binding molecule or converted to product can be accurately determined to assess the effects of potential antagonists. Potential antagonists include small organic molecules, peptides, polypeptides, and antibodies that bind to a polypeptide of the invention and thereby inhibit or eliminate its activity. Potential antagonists may also be small organic molecules, peptides, polypeptides, such as closely related proteins or antibodies, which bind to the same site on the binding molecule but induce the activity induced by gluS. Does, and thus interferes with the action of gluS by excluding it from binding. Potential antagonists include small molecules that bind to and occupy the binding site of the polypeptide, thereby preventing binding to cellular binding molecules, thereby disrupting normal biological activity. Examples of small molecules include, but are not limited to, small organic molecules, peptides, peptide-like molecules, and the like. Other potential antagonists include antisense molecules and the like (for descriptions of these molecules, see Okano, J., Neurochem. 56: 560 (1991); Oligodeoxy-nucleotides as Antisense Inhibitors of Gene Expression, CRC Press, Bockalaton, Florida (1988)). Preferred potential antagonists include gluS-related compounds and gluS variants. Each of the DNA sequences provided herein may be used in the discovery and development of antibacterial compounds. The encoded protein, when expressed, can be used as a target for screening for antibacterial agents. Furthermore, an antisense sequence is constructed using a DNA sequence encoding the amino-terminal region of the encoded protein or the Shine-Dalgarno sequence or other translation-enhancing sequence of each mRNA to control the expression of the target coding sequence. You can also. The present invention provides the use of the polypeptides, polynucleotides or inhibitors of the present invention to disrupt the etiology involved in the sequelae of infection and the initial physical interaction between mammalian hosts. In particular, the molecules of the present invention may be used to prevent bacterial attachment to mammalian extracellular matrix proteins on internal devices or extracellular matrix proteins in wounds, in particular the prevention of Gram-positive bacterial attachment; for example, phosphorylation of mammalian tyrosine kinases. Initiation blocks gluS protein-mediated entry into mammalian cells (Rosenshine et al., Infect. Immunol. 60: 2211 (1992)); between the mammalian extracellular matrix protein and the bacterial gluS protein. Block bacterial adhesion that mediates tissue damage; can be used to block the progression of normal pathologies in infections, initiated by other than implantation of an indwelling device or other surgical methods. The antagonists and agonists of the present invention may be used, for example, in infections, especially bacterial infections, especially otitis media, conjunctivitis, pneumonia, bacteremia, meningitis, sinusitis, empyema and endocarditis, most particularly for example in cerebrospinal fluid. It may be used to control and treat diseases such as meningitis such as infections. Vaccine Another aspect of the invention relates to a method of inducing an immunological response in an individual, especially a mammal, for protecting an individual from infection, particularly bacterial infection, most particularly Streptococcus pneumoniae infection. And / or a fragment or variant thereof sufficient to generate an antibody and / or a T cell immune response. Also provided is a method wherein such an immunological response slows bacterial replication. Yet another aspect of the present invention relates to a method of inducing an immunological response in an individual, the method comprising the steps of in vivo transducing gluS, or a fragment or variant thereof, whether or not the disease has been established in the individual. A nucleic acid vector that directs the expression of gluS or a fragment or variant thereof for expression is delivered to such an individual to generate, for example, an antibody and / or a T cell immune response (eg, a cytokine producing T cell or a cytotoxic T cell). Inducing an immunological response to produce antibodies that protect the individual from disease. A method for rapidly administering a gene into a desired cell includes coding on a particle. Such nucleic acid vectors may include DNA, RNA, modified nucleic acids, or DNA / RNA hybrids. A further aspect of the present invention is that an immunological response can be induced in a host or, when introduced into an induced host, induces an immunological response to gluS or a protein encoded thereby in said host. With respect to biological compositions, the compositions comprise recombinant gluS or the protein encoded thereby, and DNA that encodes and expresses an antigen against gluS or the protein encoded thereby. The immunological response may be used therapeutically or prophylactically, and the immunological response may be CTL or CD4 ⁺ It may be in the form of antibody immunity or cellular immunity, such as that generated from T cells. The gluS polypeptides or fragments thereof are combined with a co-protein capable of stabilizing the first protein but producing a fusion protein having immunogenic and protective properties, but which does not itself produce antibodies. They may be fused. Preferably, such a fusion recombinant protein solubilizes antigen co-proteins, such as lipoprotein D from Hemophilus influenzae, coexisting proteins such as glutathione-S-transferase (GST) or beta-galactosidase, And relatively large coexisting proteins that promote their production and purification. In addition, the co-protein can act as an adjuvant in the sense that it provides a universal stimulus in the immune system. The coexisting protein may be bound to either the amino or carboxy terminus of the first protein. The present invention relates to compositions, especially vaccine compositions, and methods comprising a polypeptide or polynucleotide of the invention and an immunostimulatory DNA sequence as described in Sato Y. et al., Science 273: 352 (1966). provide. The present invention has also been described, in an animal model infected with Streptococcus pneumoniae, as having been described which encodes a constant region of a bacterial cell surface protein in a DNA construct used for such genetic immunization experiments. Or, inter alia, methods of using fragments thereof are provided, which are particularly useful for identifying protein epitopes capable of stimulating a prophylactic or therapeutic immune response. This study is particularly valuable from the essential organs of animals that have succeeded in resisting and clearing bacterial infections in mammals, especially humans, for the development of preventive or therapeutic treatments for bacterial infections, especially Streptococcus pneumoniae infections. It will be possible to prepare monoclonal antibodies successfully. The polypeptide may be used as an antigen for host inoculation to obtain a specific antibody that protects against bacterial invasion, for example by inhibiting bacterial attachment to damaged tissue. Examples of tissue damage include skin or connective tissue wounds caused by, for example, mechanical, chemical or thermal damage, or by implantation of an indwelling device, or mucous membranes such as mouth, mammary gland, urethra or vaginal wounds. is there. The invention also includes a vaccine formulation that includes the immunogenic recombinant protein together with a suitable carrier. Since the protein can be degraded in the stomach, it is preferably administered parenterally, for example, subcutaneously, intramuscularly, intravenously or intradermally. Formulations suitable for parenteral administration include aqueous or non-aqueous sterilization which may contain antioxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the body fluids of the individual, preferably blood. Injectable solutions and sterile aqueous or non-aqueous suspensions which may contain suspending or thickening agents, and the like. The formulations may be presented in single-dose or multi-dose containers, for example, sealed ampules and vials, and stored in a lyophilized condition requiring only the addition of a sterile liquid carrier immediately before use. Vaccine formulations may also contain adjuvant systems that increase the immunogenicity of the formulation, such as oil-in-water or other systems well known in the art. The dosage depends on the specific activity of the vaccine and can be readily determined by routine experimentation. Although the invention has been described with respect to particular gluS proteins, the invention relates to naturally occurring proteins and fragments of similar proteins with additions, deletions or substitutions that do not substantially affect the immunogenic properties of the recombinant protein. It will be understood that it includes. Compositions, Kits and Administration The present invention also relates to compositions comprising the above-described polynucleotides or polypeptides, or agonists or antagonists thereof. The polypeptides of the present invention can be used in admixture with non-sterile or sterile carriers used for cells, tissues or organisms, for example, with a pharmaceutical carrier suitable for administration to a subject. Such compositions comprise, for example, a solvent additive or a therapeutically effective amount of a polypeptide of the invention, and a pharmaceutically acceptable carrier or excipient. Such carriers include, but are not limited to, saline, buffered saline, dextrose, water, glycerol, ethanol, and combinations thereof. The formulation should suit the mode of administration. The present invention further relates to diagnostic and pharmaceutical packs and kits comprising one or more containers filled with one or more of the above-described compositions of the present invention. The polypeptides of the present invention and other compounds may be used alone or in combination with other compounds such as therapeutic compounds. The pharmaceutical composition may be administered by any effective and convenient method, for example, topically, orally, vaginally, intravenously, intraperitoneally, intramuscularly, subcutaneously, intranasally, or intradermally. . In therapy or as a prophylactic, the active substance can be administered to the individual as an injectable composition, for example, preferably as an isotonic sterile aqueous dispersion. Alternatively, the compositions may be formulated for topical application, for example, in the form of ointments, creams, lotions, eye ointments, eye drops, ear drops, mouthwashes, impregnated bandages and suture threads, and aerosols. Ointments and creams may contain suitable conventional additives such as preservatives, solvents to aid penetration of the drug, and ointments and creams. Such topical formulations may contain compatible conventional carriers, such as cream or ointment bases and, for lotions, ethanol or oleyl alcohol. Such carriers may represent from about 1% to about 98% by weight of the formulation, more usually up to about 80% by weight of the formulation. For administration to mammals, especially humans, the daily dose of active substance is between 0.01 mg / kg and 10 mg / kg, typically around 1 mg / kg. The physician will always determine the actual dosage which will be most suitable for the individual and will vary according to age, weight and especially the individual's responsiveness. The above dosages are typical of the average case. Of course, there are individual examples where the high and low dose ranges fit, and such examples are within the scope of the present invention. Indwelling devices include surgical implants, prosthetic devices, catheters, and the like, that is, those that are introduced into the body of an individual and remain in place for an extended period of time. Such devices include, for example, artificial joints, heart valves, pacemakers, vascular grafts, vascular catheters, cerebrospinal fluid shunts, urinary catheters, continuous ambulatory peritoneal dialysis (CAPD) catheters, and the like. . The compositions of the present invention may be administered by injection to achieve a systemic effect against relevant bacteria shortly before insertion of the indwelling device. After surgery, treatment may continue for as long as the device is present in the body. In addition, it can be used on covers that spread during surgical procedures to protect against bacterial wound infections, especially those of Streptococcus pneumoniae. Many orthopedic surgeons believe that humans with prosthetic joints should be considered for antibiotic prophylaxis before dental treatments that can result in bacteremia. Delayed severe infection is a serious complication that sometimes leads to loss of prosthetic joints, with significant morbidity and mortality. It is therefore possible in this context to extend the use of active substances as an alternative to prophylactic antibiotics. In addition to the treatments described above, the compositions of the present invention may generally be used as wound healing agents to prevent bacteria from adhering to exposed matrix proteins in wound tissue, and in dental treatment by antibiotics. It may be used prophylactically instead of or in combination with prophylaxis. Alternatively, the composition of the present invention may be used to bathe an indwelling device immediately prior to insertion. For soaking wounds or indwelling devices, the active substance is preferably at a concentration of 1 μg / ml to 10 mg / ml. Conveniently, the vaccine composition is in an injectable form. Conventional immune adjuvants may be used to enhance the immune response. A unit dose suitable for vaccination is 0.5-5 μg / kg of antigen, and such doses are preferably administered 1-3 times at 1-3 week intervals. For the compounds of the present invention, no adverse toxicological effects are observed that would prevent administration to appropriate individuals in the dosage ranges indicated. Each document disclosed herein is considered to be incorporated herein by reference in its entirety. Any patent application for which this application claims priority is deemed to be incorporated herein by reference in its entirety. EXAMPLES The following examples, except as described in detail, are performed using standard techniques well known to those skilled in the art. The examples are given for illustrative purposes only and do not limit the invention. Example 1: Selection of strain, production of library and sequencing The polynucleotide having the DNA sequence shown in SEQ ID NO: 1 was used to prepare a live clone of a chromosomal DNA of Streptococcus pneumoniae in E. coli. Obtained from Rally. In some cases, flanking DNA sequences of SEQ ID NO: 1 have been constructed using sequencing data from two or more clones containing overlapping Streptococcus pneumoniae DNA. The library can be produced by a usual method, for example, the following methods 1 and 2. Total cellular DNA is isolated from Streptococcus pneumoniae 0100993 according to standard methods and size fractionated by one of two methods. Method 1 Whole cell DNA is mechanically sheared through an injection needle to size fractionate according to standard methods. Fragments up to 11 kbp in size are blunt-ended by treatment with exonuclease and DNA polymerase and an EcoRI linker is added. The fragment is ligated into the vector Lambda ZapII that has been cut with EcoRI, the library is packaged by standard methods, and E. coli is then packaged with the packaged library. Infect E. coli. The library is amplified by standard methods. Method 2 Whole cell DNA is partially hydrolyzed with one restriction enzyme or a combination of restriction enzymes that appropriately yields a series of fragments for cloning into a library vector (eg, RsaI, PalI, AluI, Bshl235I), Such fragments are size fractionated according to standard methods. An EcoRI linker is ligated to the DNA and the fragment, then ligated to the vector Lambda ZapII that has been cut with EcoRI, the library is packaged by standard methods, and E. coli Infect E. coli. The library is amplified by standard methods. Example 2 Characterization of GluS Aminoacyl measuring enzyme-mediated incorporation of radiolabeled amino acids into tRNA as trichloroacetic acid precipitable radioactivity from radiolabeled amino acids in the presence of tRNA and ATP May be measured by a chemical method (Hughes J, Mellows G and Soughton S, 1980, FEBS Letters, 122: 322-324). Thus, an inhibitor of glutamyl tRNA synthetase can be detected by a decrease in trichloroacetic acid precipitable radioactivity relative to a control. Alternatively, glutamyl tRNA synthetase inhibitors can be detected using a partial PPi / ATP exchange reaction catalyzed by tRNA synthetase (measuring the production of radiolabeled ATP from PPi) (Calender R & Berg). P, 1996, Biochemistry, 5, 1681-1690).

──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. ⁷ Identification symbol FI Theme coat ゛ (Reference) A61P 31/04 C12N 1/15 C07K 16/12 1/19 C12N 1/15 1/21 1/19 9 / 12 1/21 C12Q 1/48 5/10 C12R 1:46) 9/12 C12N 15/00 ZNAA C12Q 1/48 5/00 A // (C12N 15/09 ZNA A61K 37/02 C12R 1:46) C12R 1:46) (72) Inventor Wang Min No. 302 Centennial Drive, Blue Bell, Pennsylvania, United States 19422

Claims (1)

[Claims]   1. (A) a polypeptide encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2 A polynucleotide having at least 70% identity to the nucleotide;   (B) a polynucleotide that is complementary to the polynucleotide of (a);   (C) gluS residue contained in the deposited strain Streptococcus pneumoniae Polynucleotides encoding the same mature polypeptide expressed by the gene A polynucleotide having at least 70% identity to   (D) at least 15 of the polynucleotides of (a), (b) or (c); Polynucleotides containing consecutive bases An isolated polynucleotide comprising a polynucleotide sequence selected from the group consisting of:   2. The polynucleotide of claim 1, which is DNA.   3. 2. The polynucleotide of claim 1, which is an RNA.   4. 3. The polynucleotide of claim 2, comprising the nucleic acid sequence set forth in SEQ ID NO: 1.   5. 3. The polynucleotide of claim 2, comprising the nucleotide set forth in SEQ ID NO: 1.   6. Claims 1. Encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2. 2 polynucleotide.   7. A vector comprising the polynucleotide of claim 1.   8. A host cell comprising the vector of claim 7.   9. A polypeptide encoded by the DNA from the host cell of claim 8. A method for producing a polypeptide, comprising expressing   10. A method for producing a gluS polypeptide or fragment, said method comprising: Culturing the host of claim 8 under conditions sufficient to produce the peptide or fragment. A method that includes:   11. An amino acid that is at least 70% identical to the amino acid sequence of SEQ ID NO: 2 A polypeptide comprising a noic acid sequence.   12. A polypeptide comprising the amino acid sequence shown in SEQ ID NO: 2.   13. An antibody against the polypeptide of claim 11.   14． An antagonist that inhibits the activity or expression of the polypeptide of claim 11. .   15. Administering to the individual a therapeutically effective amount of the polypeptide of claim 11. , A method of treating an individual in need of a gluS polypeptide.   16. Administering to the individual a therapeutically effective amount of the antagonist of claim 14. A method for treating an individual in need of inhibition of a gluS polypeptide.   17． A disease associated with the expression or activity of the polypeptide of claim 11 in an individual. A method of diagnosing a disease,   (A) determining the nucleic acid sequence encoding the polypeptide; and / or Or   (B) analyzing for the presence or amount of the polypeptide in a sample from the individual. When A method that includes   18. Interacting with the polypeptide of claim 11 to inhibit or inhibit its activity A method for identifying a compound to be   A polypeptide, under conditions that allow the interaction between the compound and the polypeptide, The interaction of the compound with the compound to be screened to assess Such an interaction is a detectable signal in response to the interaction of the polypeptide with the compound Associated with the second component, which can provide   The presence of a signal resulting from the interaction of the compound with the polypeptide or By detecting the absence, the compound interacts with the polypeptide and To determine whether to activate or inhibit sex A method that includes:   19. A method for inducing an immunological response in a mammal, comprising the steps of: Or sufficient to provoke a T cell immune response to protect the animal from disease. A gluS polypeptide, or a fragment or variant thereof, into a mammal A method that includes doing.   20. A method for inducing an immunological response in a mammal, comprising: The peptide or fragment or variant thereof can be expressed in vivo to Causing the animal to become ill by inducing an immunological response that produces a T cell immune response 12. The gluS polypeptide of claim 11 or a flag thereof to protect against A method comprising delivering a nucleic acid vector that directs the expression of a fragment or variant.