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14 pages, 2529 KiB  
Article
Short-Term Phosphorus Fertilization Alters Soil Fungal Community in Long-Term Phosphorus-Deprived Yellow Soil Paddy Fields
by Huan Yang, Yehua Yang, Huaqing Zhu, Han Xiong, Yarong Zhang, Yanling Liu, Xingcheng Huang, Yu Li and Taiming Jiang
Agriculture 2025, 15(3), 280; https://doi.org/10.3390/agriculture15030280 - 28 Jan 2025
Abstract
Phosphorus (P) in soil is important in the process by which soil microbial communities regulate soil enzyme activity. We aim to explore how short-term P fertilization affects the composition and functionality of the soil fungal community, offering insights into the complex responses of [...] Read more.
Phosphorus (P) in soil is important in the process by which soil microbial communities regulate soil enzyme activity. We aim to explore how short-term P fertilization affects the composition and functionality of the soil fungal community, offering insights into the complex responses of soil fungi to fertilization. Soil samples from a long-term experiment with no P fertilization were collected for pot experiments. The pot experiment included four treatments: non-P fertilizer (NK), chemical P fertilizer (NPK), 1/2 organic fertilizer + 1/2 chemical fertilizer (MNP), and organic fertilizer (M). High-throughput sequencing was employed to analyze the composition, diversity, and functionality of soil fungal communities. Results showed that short-term P addition significantly increased the soil fungal Shannon and Pielou e indices, with increases of 34.48%~59.00% and 29.79%~53.19%, respectively. Ascomycota and Basidiomycota were the most abundant fungal phyla, whereas Cladosporium and Emericellopsis were the most abundant genera. The main factors affecting soil fungal community composition were total nitrogen (TN) and organic matter (OM). A linear discriminant analysis effect size (LEfSe) analysis indicated that Mortierellomycota were significantly enriched under the NPK treatment. A FUNGuild analysis revealed that, compared to the NK treatment, the relative abundance of Animal Pathogen–Endophyte–Lichen Parasite–Plant Pathogen–Wood Saprotroph was reduced by 67.54%, 46.93%, and 44.10% under NPK, MNP, and M treatments, respectively. The relative abundance of Plant Pathogen was less than 1% in the NPK and the MNP treatments. These results indicate that short-term P addition increased soil nutrient levels and soil fungal community diversity. Chemical P fertilizer significantly improved the fungal community structure in yellow paddy soils, enhancing beneficial fungi and suppressing pathogens. Full article
(This article belongs to the Section Agricultural Soils)
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<p>Relative abundances of soil fungi at the phylum (<b>a</b>) and genus (<b>b</b>) levels. NK, non-P fertilizer; NPK, chemical P fertilizer; MNP, 1/2 organic fertilizer + 1/2 chemical fertilizer; M, organic fertilizer.</p>
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<p>The principal component analysis (PCA) of soil fungi at the phylum (<b>a</b>) and genus (<b>b</b>) levels. NK, non-P fertilizer; NPK, chemical P fertilizer; MNP, 1/2 organic fertilizer + 1/2 chemical fertilizer; M, organic fertilizer.</p>
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<p>The LEfSe analysis of the soil fungal communities. Only taxa meeting an LDA significance threshold of 2 for fungal communities are shown. The five rings of the cladogram represent phyla (innermost), classes, orders, families, and genera (outermost). NK, non-P fertilizer; NPK, chemical P fertilizer; MNP, 1/2 organic fertilizer + 1/2 chemical fertilizer; M, organic fertilizer.</p>
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<p>FUNGuild function prediction of soil fungal communities. NK, non-P fertilizer; NPK, chemical P fertilizer; MNP, 1/2 organic fertilizer + 1/2 chemical fertilizer; M, organic fertilizer.</p>
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<p>The redundancy analysis of soil physicochemical properties in relation to different sample groups (<b>a</b>) and fungal phyla (<b>b</b>). OM, organic matter; TN, total N; AP, available P; AK, available K. NK, non-P fertilizer; NPK, chemical P fertilizer; MNP, 1/2 organic fertilizer + 1/2 chemical fertilizer; M, organic fertilizer.</p>
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19 pages, 3972 KiB  
Article
Exploring Marine Natural Compounds: Innovative Therapeutic Candidates Against Chagas Disease Through Virtual Screening and Molecular Dynamics
by Carlos Eliel Maya-Ramírez, Asmae Saih, Alfonso Méndez Tenorio, Carlos Wong Baeza, Benjamín Nogueda Torres and Juan Carlos Santiago Hernández
Life 2025, 15(2), 192; https://doi.org/10.3390/life15020192 - 28 Jan 2025
Viewed by 114
Abstract
Chagas disease, caused by the protozoan Trypanosoma cruzi, represents a significant public health challenge, particularly in Latin America’s endemic regions. The limited efficacy and frequent adverse effects of current treatments underscore the need for novel therapeutic options. This research explores marine natural [...] Read more.
Chagas disease, caused by the protozoan Trypanosoma cruzi, represents a significant public health challenge, particularly in Latin America’s endemic regions. The limited efficacy and frequent adverse effects of current treatments underscore the need for novel therapeutic options. This research explores marine natural compounds as potential candidates for Chagas disease treatment using virtual screening and in silico evaluation methods. Techniques such as molecular docking, drug-likeness evaluation, and pharmacokinetic analysis were employed to identify promising anti-parasitic compounds. Among the candidates, chandrananimycin A, venezueline A, and dispacamide demonstrated high binding affinities to key targets in T. cruzi alongside favorable docking scores and compliance with essential drug-likeness criteria. Pharmacokinetic profiling further supported their therapeutic potential, revealing desirable properties like effective absorption and minimal toxicity. These findings underscore the promise of marine-derived compounds as a valuable source of new drugs, emphasizing the need for further in vitro and in vivo investigations to elucidate their molecular mechanisms and optimize their development as viable treatments for Chagas disease. Full article
(This article belongs to the Section Pharmaceutical Science)
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<p>2D interaction map of TcBDF2 bromodomain–ligand complexes. The color code is shown that indicates the type of interaction generated in Discovery Studio, and each complex is also indicated according to the corresponding number in <a href="#life-15-00192-t003" class="html-table">Table 3</a>.</p>
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<p>RMSD plot of the ligands, the Y axis in angstroms, and the X axis in nanoseconds indicates the evolution of ligand stability with respect to the protein and its pocket. The plot shows the values of Complexes 8, 23, and 31 and the reference ligand (bromosporine).</p>
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<p>Protein RMSF profiles for the Compound 8, 23, and 31 and bromosporine complexes.</p>
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<p>ROG profiles for Compounds 8, 23, and 31 and bromosporine complexes.</p>
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<p>SASA (solvent accessible surface area) profiles for Compounds 8, 23, and 31 and bromosporine complexes.</p>
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<p>HBONDS (hydrogen bonds) profiles for Compounds 8, 23, and 31 and bromosporine complexes.</p>
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<p>PCA (principal component analysis) profiles for Compounds 8, 23, and 31 and bromosporine complexes.</p>
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<p>DCCM (dynamic cross-correlation matrix) profiles for Compounds 8, 23, and 31 and bromosporine complexes.</p>
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15 pages, 2834 KiB  
Article
Populations of Heterodera schachtii Differ in Susceptibility to Rhizosphere Bacteria Structured by Plant Age
by Rasha Haj Nuaima, Eva Tanneau and Holger Heuer
Microorganisms 2025, 13(2), 289; https://doi.org/10.3390/microorganisms13020289 - 28 Jan 2025
Viewed by 198
Abstract
Rhizosphere microbes, particularly bacteria, are essential for controlling plant-parasitic nematodes (PPNs) through various mechanisms. However, the plant’s age and the genetic composition of nematode populations can significantly influence the inhibitory effectiveness of these microbes against the beet cyst nematode Heterodera schachtii. In [...] Read more.
Rhizosphere microbes, particularly bacteria, are essential for controlling plant-parasitic nematodes (PPNs) through various mechanisms. However, the plant’s age and the genetic composition of nematode populations can significantly influence the inhibitory effectiveness of these microbes against the beet cyst nematode Heterodera schachtii. In this study, rhizosphere microbes were isolated from 39-day-old and 69-day-old resistant oilseed radish plants to evaluate their impact on the penetration of the second-stage juveniles (J2s) originating from four genetically distinct H. schachtii populations. The suppression of J2s penetration by the attached microbes varied across the nematode populations, which displayed differing levels of aggressiveness toward the resistant oilseed radish. Furthermore, differences in the alpha and beta diversity of rhizosphere bacteria were observed between the 39-day-old and 69-day-old plants, leading to variations in the bacterial attachment among the four nematode populations. In summary, the effectiveness of resistant catch crops against H. schachtii is influenced by the pathogenicity of the nematode populations and their interactions with the rhizosphere microbial community shaped by the plant’s age. Full article
(This article belongs to the Section Plant Microbe Interactions)
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<p>The bacterial attachment to J2s originated from four populations of <span class="html-italic">H. schachtii</span> (Kerpen-Buir, Elsdorf, and Acholshausen from Germany, and one from Ireland). The number of colony-forming units (CFU) formed by bacterial cells attached to J2 was determined after incubation at 28 °C overnight in the rhizosphere suspension of 39-day-old resistant oilseed radish “Colonel”. Different letters indicate significant differences in the counts of CFU/J2 among populations (Wilcoxon test, <span class="html-italic">t</span>-test, <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 12).</p>
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<p>The effect of the rhizosphere microbes isolated from 39-day-old plants of resistant oilseed radish “Colonel” on J2 penetration of <span class="html-italic">H. schachtii</span> populations into roots of 7-day-old oilseed radish “Colonel”. Comparisons were carried out within the same population across different treatments indicated by lowercase letters or between different populations within the same treatment indicated by uppercase letters (Wilcoxon test, <span class="html-italic">t</span>-test, <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 6).</p>
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<p>The effect of rhizosphere microbes isolated from 69-day-old resistant oilseed radish “Colonel” plants on J2s penetration of <span class="html-italic">H. schachtii</span> into the roots of 7-day-old oilseed radish “Colonel”. Comparisons were made within the same population across different treatments indicated by lowercase letters and between populations within the same treatment indicated by uppercase letters (Wilcoxon test, <span class="html-italic">t</span>-test, <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 6).</p>
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<p>Relative abundances of rhizosphere bacteria at the phylum level, isolated from 39-day-old (p1) and 69-day-old (p2) resistant oilseed radish (Colonel) and attached to J2s originating from four populations of <span class="html-italic">H. schachtii</span>. Each population is represented by four sample replicates per treatment. The bar chart illustrates the top 11 bacterial communities with the highest relative abundances.</p>
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<p>Shannon indices calculated for bacterial diversity of 16S rRNA, based on Illumina sequencing of rhizosphere bacteria isolated from 39-day-old (<b>A</b>) and 69-day-old (<b>B</b>) resistant oilseed radish “Colonel”. The bacteria were attached to J2s originating from four populations of <span class="html-italic">H. schachtii</span>. Each population is represented by four sample replicates per treatment. Different lowercase letters indicate significant differences in diversity among population-attached bacteria and rhizosphere bacteria within the same treatment, while different uppercase letters indicate significant differences between the two treatments for the same population or rhizosphere bacteria (Wilcoxon test, <span class="html-italic">t</span>-test, <span class="html-italic">p</span> &lt; 0.05, <span class="html-italic">n</span> = 4).</p>
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<p>Heatmap of beta diversity for rhizosphere bacteria isolated from 39-day-old (Rhizosphere 1) and 69-day-old (Rhizosphere 2) resistant oilseed radish “Colonel” and attached to J2s originating from four populations of <span class="html-italic">H. schachtii</span>. Each population is represented by four sample replicates per treatment. The two values in each grid cell represent the weighted (quantitative) and unweighted (qualitative) UniFrac distances, respectively.</p>
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17 pages, 3029 KiB  
Article
Evaluation of Serum Supplementation on the Development of Haemonchus contortus Larvae In Vitro and on Compound Screening Results
by Sandani S. Thilakarathne, Aya C. Taki, Tao Wang, Cameron Nowell, Bill C. H. Chang and Robin B. Gasser
Int. J. Mol. Sci. 2025, 26(3), 1118; https://doi.org/10.3390/ijms26031118 - 28 Jan 2025
Viewed by 243
Abstract
A high-throughput platform for assessing the activity of synthetic or natural compounds on the motility and development of Haemonchus contortus larvae has been established for identifying new anthelmintic compounds active against strongylid nematodes. This study evaluated the impact of serum supplementation on larval [...] Read more.
A high-throughput platform for assessing the activity of synthetic or natural compounds on the motility and development of Haemonchus contortus larvae has been established for identifying new anthelmintic compounds active against strongylid nematodes. This study evaluated the impact of serum supplementation on larval development, motility and survival in vitro and its implications for phenotypic compound screening. Of five blood components assessed, 7.5% sheep serum significantly enhanced larval development, motility and survival compared to the original medium (LB*), leading to the formulation of an improved medium (LBS*). Proteomic analysis revealed marked differences in protein expression in larvae cultured in LBS* versus LB*, including molecules associated with structural integrity and metabolic processes. The phenotypic screening of 240 compounds (“Global Priority Box” from Medicines Malaria Venture) using LBS* yielded results distinct from those in LB*, highlighting the effect of culture conditions on screening assessments. These findings indicate/emphasise the critical need to evaluate and optimise culture media for physiologically relevant conditions in screening platforms, improving the reliability of anthelmintic discovery. Full article
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<p>Evaluation of the growth/development, motility and survival of <span class="html-italic">H. contortus</span> larvae in vitro in the presence or absence of serum. (<b>A</b>) Graphs showing the mean length and width of larvae (mean ± standard deviation, SD) maintained in culture medium LB* or LBS*—data derived from two independent experiments. (<b>B</b>) Motility of larvae in LB* or LBS* measured using established methods (<a href="#sec2dot3-ijms-26-01118" class="html-sec">Section 2.3</a>)—data points represent 18 replicates; mean ± standard error of the mean (SEM). Statistical analysis was conducted using non-parametric (Kruskal–Wallis) one-way ANOVA or Dunn’s multiple comparison test. A black arrow indicates the optimum percentage (7.5%) of serum. *** indicates a significant difference (<span class="html-italic">p</span> &lt; 0.001), and ns is not significant. (<b>C</b>) Representative images of larvae in LB* or LBS* exposed to Sytox Green stain with reference to larvae exposed to the positive control compound M-666; 4-times magnification (fluorescent green = dead). M-666 likely acts on the respiratory chain and is lethal to larvae (for xL3, IC<sub>50</sub> = 0. 19 µM; for L4, IC<sub>50</sub> = 0.002 µM; cf. [<a href="#B38-ijms-26-01118" class="html-bibr">38</a>,<a href="#B39-ijms-26-01118" class="html-bibr">39</a>]).</p>
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<p>(<b>A</b>) Representative images of larvae of <span class="html-italic">Haemonchus contortus</span> in LB* and LBS* cultured for 168 h or 336 h and subsequently stained with iodine (10-times magnification) or Hoechst 33342 (20×/NA0.75 DRY objective). Anus (black arrow) and genital primordium (purple asterisk) are indicated (scale bar = 50 µm). Although larvae cultured in LB* did not exhibit sexual differentiation, those cultured in LBS* displayed clear dimorphism, in accordance with those originally described by Veglia [<a href="#B6-ijms-26-01118" class="html-bibr">6</a>]. In female larvae, the genital primordium was consistently positioned closer to the anus, whereas in male larvae, it was located approximately midway along the body. (<b>B</b>) Genital primordium of representative larvae in LB* or LBS* at 168 h observed using 25×/NA0.95 WATER objective (Leica Microsystems; ~70-times magnification; scale bar = 20 µm).</p>
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<p>Results of the primary screen of the Global Health Priority Box compounds (n = 240) against exsheathed third-stage larvae (xL3s) of <span class="html-italic">Haemonchus contortus</span> using medium LB* (<b>A</b>) and LBS* (<b>B</b>). All test and positive control compounds were tested at 20 µM. Each dot represents an individual test compound. Mean ± standard error of the mean (SEM) indicated for negative and positive control compounds (eight data points for monepantel, and four for moxidectin and M-666) and negative controls (16 data points for LB* and LBS*). The Z′-factor calculated was 0.83.</p>
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<p>Analyses of somatic proteomes and differentially expressed proteins in the larvae of <span class="html-italic">Haemonchus contortus</span> cultured in medium LB* or LBS* for 168 h. (<b>A</b>) A heatmap showing relative protein abundance in larvae incubated in LB* or LBS*. Protein abundance (low to high) is shown in light to dark blue. Rows indicate individual proteins. Columns indicate six replicate samples representing larvae cultured in LB* (i.e., LB*1 to LB*6) or LBS* (LBS*1 to LBS*6). (<b>B</b>) Volcano plots of differentially expressed proteins identified between the LB* vs. LBS* (difference LB*-LBS*). Proteins that were upregulated and downregulated were in blue and purple, respectively. Proteins that were not significant are indicated in grey. Log<sub>2</sub> (fold change) ≥ 2 and adjusted (<span class="html-italic">p</span>-value) ≤ 0.05. (<b>C</b>) The pie chart showing the distribution of the molecular functions (gene ontology (GO) level 2) of proteins quantified in larvae in LBS*. (<b>D</b>) Enriched biological processes and associated pathways (<span class="html-italic">Kyoto Encyclopedia of Genes and Genomes</span>, KEGG) of differentially expressed proteins in larvae LBS*. KEGG pathways sorted according to the numbers (in ascending order) of proteins in the main categories: orange (A09120—genetic information processing), blue (A09100—metabolism) and brown (A09150—organismal systems).</p>
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26 pages, 2753 KiB  
Article
Duplication of a Type-P5B-ATPase in Laverania and Avian Malaria Parasites and Implications About the Evolution of Plasmodium
by Mark F. Wiser
Parasitologia 2025, 5(1), 6; https://doi.org/10.3390/parasitologia5010006 - 27 Jan 2025
Viewed by 376
Abstract
Two related P-type ATPases, designated as ATPase1 and ATPase3, were identified in Plasmodium falciparum. These two ATPases exhibit very similar gene and protein structures and are most similar to P5B-ATPases. There are some differences in the predicted substrate-binding sites of ATPase1 and [...] Read more.
Two related P-type ATPases, designated as ATPase1 and ATPase3, were identified in Plasmodium falciparum. These two ATPases exhibit very similar gene and protein structures and are most similar to P5B-ATPases. There are some differences in the predicted substrate-binding sites of ATPase1 and ATPase3 that suggest different functions for these two ATPases. Orthologues of ATPase3 were identified in all Plasmodium species, including the related Hepatocystis and Haemoproteus. ATPase3 orthologues could also be identified in all apicomplexan species, but no clear orthologues were identified outside of the Apicomplexa. In contrast, ATPase1 orthologues were only found in the Laverania, avian Plasmodium species, and Haemoproteus. ATPase1 likely arose from a duplication of the ATPase3 gene early in the evolution of malaria parasites. These results support a model in which early malaria parasites split into two clades. One clade consists of mammalian malaria parasites and Hepatocystis but excludes P. falciparum and related Laverania. The other clade includes Haemoproteus, avian Plasmodium species, and Laverania. This contrasts to recent models that suggest all mammalian malaria parasites form a monophyletic group, and all avian malaria parasites form a separate monophyletic group. ATPase1 may be a useful taxonomic/phylogenetic character for the phylogeny of Haemosporidia. Full article
14 pages, 291 KiB  
Article
Nutritional Potential and Low Heavy Metals Content of Oryctes monoceros (Olivier, 1789) and Rhynchophorus phoenicis (Fabricius, 1801) Adults, Two Coleopteran Species Consumed in Togo
by Fègbawè Badanaro, Narcis Barsan, Mamatchi Mélila, Kamilou Ouro-Sama, Koami Améyran, Florin-Marian Nedeff, Oana Irimia and Valentin Nedeff
Appl. Sci. 2025, 15(3), 1317; https://doi.org/10.3390/app15031317 - 27 Jan 2025
Viewed by 295
Abstract
Oryctes monoceros (Olivier, 1789) (Scarabaeidae) and Rhynchophorus phoenicis (Fabricius, 1801) (Curculionidae) are two insects generally known as formidable pests of oil palms and coconuts trees. Although little known, different developmental stages of these insects are consumed. The aim of this study is to [...] Read more.
Oryctes monoceros (Olivier, 1789) (Scarabaeidae) and Rhynchophorus phoenicis (Fabricius, 1801) (Curculionidae) are two insects generally known as formidable pests of oil palms and coconuts trees. Although little known, different developmental stages of these insects are consumed. The aim of this study is to determine the composition of these adult Coleopteran species in order to promote their consumption as a strategy for enhancing food security. Chemical analyses were carried out on adults of both species. Samples of O. monoceros and R. phoenicis were collected in three localities in Togo. The ash, protein, vitamin, and lipid contents were determined according to the AOAC reference methods. The fiber contents were obtained by the method of Weende. The minerals and heavy metals were analyzed by atomic absorption spectrophotometry and colorimetry. Fatty acid composition was determined by gas chromatography. The results showed the average protein content ranges from 44.32 ± 0.83 to 45.89 ± 0.83%. The lipid level is between 15.06 ± 0.28% and 14.64 ± 0.54. Their lipids contain unsaturated fatty acids, notably oleic (40.84 ± 0.112 vs. 40.84 ± 0.11%), linoleic (4.49 ± 0.00 vs. 5.07 ± 0.02%), and α-linolenic (5.07 ± 0.02 vs. 6.35 ± 0.01%) acid. They are excellent sources of minerals and vitamins. They are also free of heavy metals. These species could, therefore, contribute to the nutritional balance of consumers. They deserve to be better promoted for human consumption, as they could make a significant contribution to the fight against malnutrition and constitute a novel food source. Full article
16 pages, 647 KiB  
Review
Parasitism by Entomopathogenic Fungi and Insect Host Defense Strategies
by Dinghai Zhang, Haidi Qi and Feng Zhang
Microorganisms 2025, 13(2), 283; https://doi.org/10.3390/microorganisms13020283 - 27 Jan 2025
Viewed by 300
Abstract
Entomopathogenic fungi, a group of insect pathogens, are characterized by high insecticidal efficacy and minimal environmental impact. They are commonly used as biopesticides for pest control due to their significant practical value. We here classify entomopathogenic fungi according to the process of fungal [...] Read more.
Entomopathogenic fungi, a group of insect pathogens, are characterized by high insecticidal efficacy and minimal environmental impact. They are commonly used as biopesticides for pest control due to their significant practical value. We here classify entomopathogenic fungi according to the process of fungal infection in hosts, changes in host behavior during infection, and mechanisms of spore transmission, and review the strategies employed by insects to resist infection, including physical barrier defenses, immune system defenses, and behavioral avoidance of fungal pathogens. This review also discusses the pathogenic mechanisms of fungi on insects and the closely linked co-evolution between fungal pathogens and insect defenses. In conclusion, a perspective on future research is provided, emphasizing the impact of insect population density and spore concentration in the environment on disease outbreaks. Full article
(This article belongs to the Section Molecular Microbiology and Immunology)
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<p>The mechanisms of entomopathogenic fungi invading hosts. The figure depicts the infection process of entomopathogenic fungi in insects. Fungal spores attach to the insect’s surface, form appressoria to penetrate the cuticle, and develop mycelium inside the host. As the fungus spreads, it kills the host, proliferates, and produces new spores, which are then dispersed to infect other insects, completing the infection cycle.</p>
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18 pages, 2971 KiB  
Article
Efficacy of LaAg Vaccine Associated with Saponin Against Leishmania amazonensis Infection
by Mirian França de Mello, Patrícia de Almeida Machado, Pollyanna Stephanie Gomes, Gabriel Oliveira-Silva, Monique Pacheco Duarte Carneiro, Tadeu Diniz Ramos, Juliana Elena Silveira Pratti, Raquel Peralva, Luan Firmino-Cruz, Alda Maria Da-Cruz, Luciana Covre, Daniel Claúdio Oliveira Gomes, Bartira Rossi-Bergmann, Eduardo Fonseca Pinto, Alessandra Marcia da Fonseca-Martins and Herbert Leonel de Matos Guedes
Vaccines 2025, 13(2), 129; https://doi.org/10.3390/vaccines13020129 - 27 Jan 2025
Viewed by 300
Abstract
Background/Objectives: The total lysate of Leishmania amazonensis (LaAg) is one of the most extensively studied vaccine formulations against leishmaniasis. Despite demonstrating safety and immunogenicity when administered intramuscularly, LaAg has failed to show efficacy in clinical trials and, in some cases, has even been [...] Read more.
Background/Objectives: The total lysate of Leishmania amazonensis (LaAg) is one of the most extensively studied vaccine formulations against leishmaniasis. Despite demonstrating safety and immunogenicity when administered intramuscularly, LaAg has failed to show efficacy in clinical trials and, in some cases, has even been associated with an enhanced susceptibility to infection. Adjuvants, which are molecules or compounds added to antigens to enhance the immunogenicity or modulate the immune response, are frequently employed in vaccine studies. This study aimed to evaluate different adjuvants to improve the protective efficacy of LaAg in L.amazonensis infection using a BALB/c mouse model. Methods: BALB/c mice were immunized with LaAg in combination with various adjuvants. The delayed-type hypersensitivity (DTH) test was assessed by measuring the infected paw and was used to evaluate the immunogenicity and to determine the most effective adjuvant. The immune response was analyzed through flow cytometry, focusing on cytokine production, immune cell recruitment and lesion size, alongside the control of parasite load at the infection site. The expression levels of iNOS and TGF-β were quantified using RT-qPCR, while IgG1, IgG2a and IgE antibody levels were determined via ELISA. Results: Among the adjuvants tested, only saponin (SAP) elicited a significant DTH response following LaAg challenge. SAP enhanced the immunogenicity of LaAg, as evidenced by increased IFN-γ-producing CD4+ and CD8+ T cells in the draining lymph nodes at 18 h post-challenge. Additionally, SAP facilitated the recruitment of lymphocytes, macrophages, neutrophils and eosinophils to the infection site. Conclusions: The LaAg + SAP combination conferred partial protection, as demonstrated by a reduction in lesion size and the partial control of parasite load. In conclusion, the addition of SAP as an adjuvant to LaAg effectively modulates the immune response, enhancing the vaccine’s protective efficacy. These findings provide valuable insights into the development of improved vaccines against L.amazonensis infection. Full article
(This article belongs to the Special Issue Recent Advances in Vaccine Adjuvants and Formulation)
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<p>DTH response in BALB/c immunized with LaAg and different adjuvants. BALB/c mice were vaccinated twice, with an interval of one week between doses, intramuscularly with 100 μg of LaAg alone or associated with different adjuvants, namely CFA (80 µL/dose), SAP (100 μg/dose) or AddaVax<sup>TM</sup> (50 µL/dose); in the control group, 100 μL of PBS was used. One week after the last vaccine dose, they were challenged in the footpad with LaAg, <span class="html-italic">L.amazonensis</span> or <span class="html-italic">L.amazonensis</span> and LaAg. Swelling was measured at times of 0, 18, 24 and 48 h after challenge. (<b>A</b>) Challenge with 100 μg LaAg. (<b>B</b>) Challenged with live <span class="html-italic">L.amazonensis</span> in stationary phase (2 × 10<sup>6</sup> promastigotes). (<b>C</b>) Challenged with live <span class="html-italic">L.amazonensis</span> in stationary phase (2 × 10<sup>6</sup> promastigotes) and 1 week after new challenge with 10 μg of LaAg. These results refer to one independent experiment and each group consisted of five animals. Results were expressed as mean ± SD (<span class="html-italic">n</span> = 5). * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 in relation to the PBS group.</p>
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<p>Phenotypic analysis of IFN-γ-, IL-10- and IL-4-producing CD4<sup>+</sup> and CD8<sup>+</sup> T cells in BALB/c mice vaccinated with LaAg + SAP. BALB/c mice were vaccinated twice intramuscularly, with an interval of 1 week between doses, and euthanized 3 days after the second vaccine dose. Phenotypic analysis of popliteal lymph nodes was carried out. Frequency (<b>A</b>) and absolute number (<b>B</b>) of IFN-γ-producing CD4<sup>+</sup> cells. Frequency (<b>C</b>) and absolute number (<b>D</b>) of IFN-γ-producing CD8<sup>+</sup> cells. Frequency (<b>E</b>) and absolute number (<b>F</b>) of IL-10-producing CD4<sup>+</sup> cells. Frequency (<b>G</b>) and absolute number (<b>H</b>) of IL-10-producing CD8<sup>+</sup> cells. Frequency (<b>I</b>) and absolute number (<b>J</b>) of IL-4-producing CD4<sup>+</sup> cells. Frequency (<b>K</b>) and absolute number (<b>L</b>) of IL-4-producing CD8<sup>+</sup> cells. These results refer to one independent experiment, with five animals per group. Results were obtained using FlowJo software and expressed as mean ± SD (<span class="html-italic">n</span> = 5). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 in relation to the PBS group.</p>
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<p>Antibody levels increased in mice vaccinated with LaAg + SAP. BALB/c mice were vaccinated twice intramuscularly, with an interval of 1 week between doses and euthanization 3 days after the second vaccine dose. The levels of IgG1, IgG2a and IgE antibodies in the plasma of the animals were determined. (<b>A</b>) IgG1 antibody level. (<b>B</b>) IgG2a antibody level. (<b>C</b>) IgE antibody level. This result refers to one independent experiment, with five animals per group. Results were expressed as mean ± SD. *** <span class="html-italic">p</span> &lt; 0.001 in relation to the PBS group.</p>
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<p>Cutaneous DTH and vascular permeability in BALB/c mice previously immunized with LaAg + SAP and their immunogenic controls, and after being challenged with <span class="html-italic">L.amazonensis</span>. (<b>A</b>) Illustrative photographs of the representative footpads of each group (there was no distance parameter control for photography) 18 h after challenge. These results refer to three independent experiments, with five animals per group. (<b>B</b>) Optical density (O.D.) of Evans blue dye. The data represent the subtraction of the O.D. of infected footpads to uninfected footpads. These data refer to one independent experiment, with three animals per group. All these results were expressed as mean ± SD. * <span class="html-italic">p</span> &lt; 0.05 in relation to the PBS group.</p>
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<p>Histology of the footpads of BALB/c mice vaccinated with LaAg + SAP and challenged with <span class="html-italic">L.amazonensis</span>. BALB/c mice were immunized, infected with <span class="html-italic">L.amazonensis</span> and 18 h after challenge, the animals were euthanized. The infected footpads were fixed in paraformaldehyde and decalcified with EDTA. Sections of 4 μm were made followed by hematoxylin and eosin staining for counting. (<b>A</b>) Total cell count. (<b>B</b>) Neutrophils/field. (<b>C</b>) Eosinophils/field. (<b>D</b>) Macrophages/field. (<b>E</b>) Lymphocytes/field. (<b>F</b>) Mast cells/field. These results refer to one independent experiment, with five animals per group. The results were expressed as mean ± SD (<span class="html-italic">n</span> = 5). * <span class="html-italic">p</span> &lt; 0.05 and ** <span class="html-italic">p</span> &lt; 0.01 in relation to the PBS group.</p>
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<p>Phenotypic analysis of IFN-γ-, IL-10- and IL-4-producing CD4<sup>+</sup> and CD8<sup>+</sup> T cells in BALB/c mice vaccinated with LaAg + SAP and challenged with <span class="html-italic">L.amazonensis</span>. BALB/c mice were vaccinated twice intramuscularly, with an interval of one week between doses, challenged with <span class="html-italic">L.amazonensis</span> seven days after the last dose and euthanized 18 h after challenge. Phenotypic analysis of the popliteal lymph nodes was carried out. Frequency (<b>A</b>) and absolute number (<b>B</b>) of IFN-γ-producing CD4<sup>+</sup> cells. Frequency (<b>C</b>) and absolute number (<b>D</b>) of IFN-γ-producing CD8<sup>+</sup> cells. Frequency (<b>E</b>) and absolute number (<b>F</b>) of IL-10-producing CD4<sup>+</sup> cells. Frequency (<b>G</b>) and absolute number (<b>H</b>) of IL-10-producing CD8<sup>+</sup> cells. Frequency (<b>I</b>) and absolute number (<b>J</b>) of IL-4-producing CD4<sup>+</sup> cells. Frequency (<b>K</b>) and absolute number (<b>L</b>) of IL-4-producing CD8<sup>+</sup> cells. These results refer to one independent experiment, with five animals per group. Results were obtained using the FlowJo software and expressed as mean ± SD (<span class="html-italic">n</span> = 5). * <span class="html-italic">p</span> &lt; 0.05 in relation to the PBS group.</p>
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<p>Efficacy of the LaAg + SAP vaccine in protecting against <span class="html-italic">L.amazonensis</span> infection in BALB/c mice. (<b>A</b>) Lesion size that was followed for 50 days after infection. Footpad thicknesses were monitored weekly by pachymetry. (<b>B</b>) Parasite load on day 50 after infection; the result is expressed as the relative fluorescence units from macerated footpads infected with <span class="html-italic">L.amazonensis</span> (GFP). (<b>C</b>) limited dilution assay analysis of parasite load. These results refer to one independent experiment, with five animals per group. Results were expressed as mean ± SD (<span class="html-italic">n</span> = 5). * <span class="html-italic">p</span> &lt; 0.05 in relation to the PBS group.</p>
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15 pages, 1509 KiB  
Article
The First Detection of Parasite Ellobiopsis sp. on Calanoids (Crustacea: Copepoda) Inhabiting the Caspian Sea (Central Asia: West Kazakhstan)
by Moldir Aubakirova, Saule Zh. Assylbekova, Kuanysh B. Isbekov, Arkady Kim, Ainur A. Zhaksylykova and Zamira Bolatbekova
Diversity 2025, 17(2), 91; https://doi.org/10.3390/d17020091 - 27 Jan 2025
Viewed by 252
Abstract
The data on hosts of Ellobiopsis in Central Asia waterbodies are nearly non-existent. All research in this direction was conducted in other regions (Europe and Brazil). Parasitological studies were carried out in different seasons in the North and Middle Caspian Sea. Twenty-one taxa [...] Read more.
The data on hosts of Ellobiopsis in Central Asia waterbodies are nearly non-existent. All research in this direction was conducted in other regions (Europe and Brazil). Parasitological studies were carried out in different seasons in the North and Middle Caspian Sea. Twenty-one taxa were registered in zooplankton, and only dominants of community calanoids Acartia (Acanthacartia) tonsa and Calanipeda aquaedulcis were infected with Ellobiopsis sp. Calanoida C. aquaedulcis was reported for the first time as a host for Ellobiopsis. The number of parasites per host was equal to one. The body length of parasites varied from 0.10 to 0.80 mm. The highest infection degree was recorded in C. aquaedulcis (5.71%), and it varied from 2.61% to 3.35% in Acartia. The individuals in the juvenile developmental stages were infected in Calanipeda, while in Acartia, individuals in all developmental stages were vulnerable to infection. The infected calanids had reduced body lengths. The findings suggest the possible influence of Ellobiopsis sp. on quantitative variables of hosts in the Middle Caspian, especially on biomass, by reducing the body sizes of hosts. However, no effect on the abundance and biomass of the host and the structure of the zooplankton of the North Caspian Sea has been detected. Full article
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<p>Map scheme of the location of the sampling stations in the North (grey triangle) and Middle (green triangle) Caspian Sea, 2024.</p>
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<p>General forms of infected <span class="html-italic">Acartia (A.) tonsa</span> and <span class="html-italic">C. aquaedulcis</span> populations. <span class="html-italic">Acartia (A.) tonsa:</span> (<b>A</b>)—male, (<b>B</b>)—female, (<b>C</b>,<b>D</b>)—juvenile copepodid (stage IV–V), (<b>E</b>)<span class="html-italic">—Ellobiopsis</span> sp. (red square—the trophomere; red circle—gonomers), (<b>F</b>)—juvenile copepodid (stage III), (<b>G</b>)—nauplii. <span class="html-italic">C. aquaedulcis:</span> (<b>H</b>)—nauplii, (<b>I</b>)—juvenile copepodid (stage IV–V), (<b>J</b>)—<span class="html-italic">Ellobiopsis</span> sp.</p>
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<p>General forms of infected <span class="html-italic">Acartia (A.) tonsa</span> and <span class="html-italic">C. aquaedulcis</span> populations. <span class="html-italic">Acartia (A.) tonsa:</span> (<b>A</b>)—male, (<b>B</b>)—female, (<b>C</b>,<b>D</b>)—juvenile copepodid (stage IV–V), (<b>E</b>)<span class="html-italic">—Ellobiopsis</span> sp. (red square—the trophomere; red circle—gonomers), (<b>F</b>)—juvenile copepodid (stage III), (<b>G</b>)—nauplii. <span class="html-italic">C. aquaedulcis:</span> (<b>H</b>)—nauplii, (<b>I</b>)—juvenile copepodid (stage IV–V), (<b>J</b>)—<span class="html-italic">Ellobiopsis</span> sp.</p>
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<p>A dendrogram of the similarity of zooplankton species composition in different periods of study of North and Middle Caspian Sea.</p>
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11 pages, 1291 KiB  
Article
Accuracy of Genomic Predictions for Resistance to Gastrointestinal Parasites in Australian Merino Sheep
by Brenda Vera, Elly A. Navajas, Elize Van Lier, Beatriz Carracelas, Pablo Peraza and Gabriel Ciappesoni
Genes 2025, 16(2), 159; https://doi.org/10.3390/genes16020159 - 26 Jan 2025
Viewed by 325
Abstract
Infection by gastrointestinal nematodes (GINs) in sheep is a significant health issue that affects animal welfare and leads to economic losses in the production sector. Genetic selection for parasite resistance has shown promise in improving animal health and productivity. This study aimed to [...] Read more.
Infection by gastrointestinal nematodes (GINs) in sheep is a significant health issue that affects animal welfare and leads to economic losses in the production sector. Genetic selection for parasite resistance has shown promise in improving animal health and productivity. This study aimed to determine if incorporating genomic data into genetic prediction models currently used in Uruguay could improve the accuracy of breeding value estimations for GIN resistance in the Australian Merino breed. This study compared the accuracy of breeding value predictions using the BLUP (Best Linear Unbiased Prediction) and ssGBLUP (single-step genomic BLUP) models on partial and complete data sets, including 32,713 phenotyped and 3238 genotyped animals. The quality of predictions was evaluated using a linear regression method, focusing on 145 rams. The inclusion of genomic data increased the average individual accuracies by 4% for genotyped and phenotyped animals. For animals with genomic and non-phenotyped data, the accuracy improvement reached 8%. Of these, one group of animals that benefited from an ssGBLUP evaluation came from a facility with a strong connection to the informative nucleus and showed an average increase of 20% in their individual accuracy. Additionally, ssGBLUP slightly outperformed BLUP in terms of prediction quality. These findings demonstrate the potential of genomic information to improve the accuracy of breeding value predictions for parasite resistance in sheep. The integration of genomic data, particularly in non-phenotyped animals, offers a promising tool for enhancing genetic selection in Australian Merino sheep to improve resistance to gastrointestinal parasites. Full article
(This article belongs to the Special Issue Genetics and Genomics of Sheep and Goat)
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<p>Workflow for comparing individual accuracies and quality estimators between BLUP and ssGBLUP models.</p>
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<p>(G)EBV accuracies in validation population (<b>A</b>) without and (<b>C</b>) with FEC phenotype. Boxplot diagrams for accuracy increase using ssGBLUP compared to BLUP in evaluations (<b>B</b>) without phenotype and (<b>D</b>) with phenotype.</p>
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16 pages, 1315 KiB  
Systematic Review
Tick Diversity and Distribution of Pathogen in Ticks Collected from Wild Animals and Vegetation in Africa
by Roland Eric Yessinou, Aldric Koumassou, Haruna Baba Galadima, Hospice Nanoukon-Ahigan, Souaïbou Farougou and Martin Pfeffer
Pathogens 2025, 14(2), 116; https://doi.org/10.3390/pathogens14020116 - 25 Jan 2025
Viewed by 470
Abstract
Ticks are important vectors of a wide range of pathogens with significant medical and veterinary importance. Different tick species occupy different habitats with an overall widespread geographical distribution. In addition to their role as reservoirs or vectors, ticks are involved in maintaining pathogens [...] Read more.
Ticks are important vectors of a wide range of pathogens with significant medical and veterinary importance. Different tick species occupy different habitats with an overall widespread geographical distribution. In addition to their role as reservoirs or vectors, ticks are involved in maintaining pathogens in the environment and among wild and domestic animals. In this study, tick species infesting wild animals, as well as collected from the environment and their pathogens reported in 17 countries in Africa between 2003 and 2023, were collected according to the PRISMA guidelines. Data on ticks resulted in a total of 40 different tick species from 35 different wild animal species. Among the ticks, 34 infectious agents were noted including parasitic (Babesia, Theileria, Hepatozoon, Eimeria), bacterial (Anaplasma, Bartonella, Borrelia, Candidatus Midichloria mitochondrii, Candidatus Allocryptoplasma spp., Coxiella, Ehrlichia, Francisella, and Rickettsia), and a surprisingly high diversity of viral pathogens (Bunyamwera virus, Crimean-Congo Haemorhagic Fever virus, Ndumu virus, Semliki Forest virus, Thogoto virus, West Nile virus). These results highlight the public health and veterinary importance of the information on tick-borne infections. This knowledge is essential to strive to implement programs for sustainable control of ticks and tick-borne diseases. Full article
(This article belongs to the Collection Advances in Tick Research)
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<p>PRISMA flow diagram describing the process of selecting eligible studies for review systematic on pathogens identified in ticks collected in wildlife and vegetation.</p>
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<p>Pathogens reported in wildlife-infesting ticks in Africa. Candidatus is either Midichloria mitochondrii or <span class="html-italic">Allocryptoplasma</span> spp. Virus is either CCHFV, Ndumu-, Bunyamwea-, Semliki Forest-, West Nile-, or Thogoto virus.</p>
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20 pages, 6451 KiB  
Article
Overcoming Printed Circuit Board Limitations in an Energy Harvester with Amplitude Shift Keying and Pulse Width Modulation Communication Decoder Using Practical Design Solutions
by Mohamad Al Sabbagh, Rony E. Amaya, Mustapha Chérif-Eddine Yagoub and Abdullah M. Almohaimeed
Electronics 2025, 14(3), 485; https://doi.org/10.3390/electronics14030485 - 25 Jan 2025
Viewed by 255
Abstract
This paper presents PCB design solutions for implementing a radiative-field RF energy harvester with an ASK-PWM decoding communication scheme using available commercial components. The paper provides the design approach and tackles key challenges such as the impact of inductive parasitic effects at the [...] Read more.
This paper presents PCB design solutions for implementing a radiative-field RF energy harvester with an ASK-PWM decoding communication scheme using available commercial components. The paper provides the design approach and tackles key challenges such as the impact of inductive parasitic effects at the output of the harvester, how to maintain the PCE at a constant value regardless of the time constant at the output of the communication path’s rectifier, and the difficulty of changing the aspect ratio of the discrete inverter used for PWM decoding. These challenges are addressed by using multiple capacitors connected in parallel at the output of the rectifier to reduce inductive parasitic effects, adding a series resistor in the communication path’s rectifier to isolate its loading from impacting the PCE, and utilizing a potentiometer in the inverter to realize PWM decoding on PCB. The system was manufactured using FR-4 substrate material with a size of 5 cm × 4 cm × 0.6 cm, harvesting energy at the ISM frequency of 924 MHz with a PCE of 42.12% at a bit rate of 15 Kbps. Moreover, the system consumes only 355 μW of power and maintains correct harvesting and decoding operation in the antenna separation range of 6–12 cm. This work aims to provide an alternative to IC realization by implementing the system entirely using commercial discrete components, reducing costs, adding flexibility, reducing development time, and allowing for simple debugging. Full article
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<p>Proposed harvesting ASK-PWM circuit with contribution highlighted in dashed boxes.</p>
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<p>Illustrative plots of ASK-PWM demodulator and decoder.</p>
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<p>Voltage doubler design in ADS: (<b>a</b>) schematic, (<b>b</b>) matching simulation, and (<b>c</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>E</mi> <mi>H</mi> </mrow> </msub> </semantics></math> (blue) and <math display="inline"><semantics> <mrow> <mi>P</mi> <mi>C</mi> <mi>E</mi> </mrow> </semantics></math> (red) simulations.</p>
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<p>Inductive parasitic effect on harvested voltage: (<b>a</b>) transient simulations of schematic without <math display="inline"><semantics> <msub> <mi>L</mi> <mi>P</mi> </msub> </semantics></math>, (<b>b</b>) schematic’s frequency response, (<b>c</b>) original layout with transient co-simulation, (<b>d</b>) original layout’s frequency response, (<b>e</b>) modified layout with transient co-simulation, and (<b>f</b>) modified layout’s frequency response.</p>
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<p>A plot showing the relationship between the RF swing at the output and the number of shunt capacitive branches with blue dashed lines highlighting successive voltage reduction.</p>
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<p>Interface between harvester and communication paths.</p>
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<p>Frequency response of the communication path: (<b>a</b>) test bench schematic, and (<b>b</b>) simulation with different <math display="inline"><semantics> <msub> <mi>C</mi> <mn>3</mn> </msub> </semantics></math> values.</p>
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<p>Transient response of the circuit in <a href="#electronics-14-00485-f006" class="html-fig">Figure 6</a> when: (<b>a</b>) <math display="inline"><semantics> <msub> <mi>C</mi> <mn>3</mn> </msub> </semantics></math> = 10 pF, and (<b>b</b>) <math display="inline"><semantics> <msub> <mi>C</mi> <mn>3</mn> </msub> </semantics></math> = 1000 pF.</p>
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<p>Voltage reduction by adjusting <math display="inline"><semantics> <msub> <mi>R</mi> <mrow> <mi>e</mi> <mi>q</mi> </mrow> </msub> </semantics></math>: (<b>a</b>) voltage drop without <math display="inline"><semantics> <msub> <mi>R</mi> <mi>M</mi> </msub> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>P</mi> <mi>C</mi> <mi>E</mi> </mrow> </semantics></math> of harvesting path without <math display="inline"><semantics> <msub> <mi>R</mi> <mi>M</mi> </msub> </semantics></math> in the communication’s path, (<b>c</b>) voltage drop with <math display="inline"><semantics> <msub> <mi>R</mi> <mi>M</mi> </msub> </semantics></math>, and (<b>d</b>) <math display="inline"><semantics> <mrow> <mi>P</mi> <mi>C</mi> <mi>E</mi> </mrow> </semantics></math> of the harvester’s path with <math display="inline"><semantics> <msub> <mi>R</mi> <mi>M</mi> </msub> </semantics></math> added in the communication’s path.</p>
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<p>ASK filter and demodulator simulations: (<b>a</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>C</mi> <mi>O</mi> <mi>M</mi> <mi>M</mi> </mrow> </msub> </semantics></math>; (<b>b</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>E</mi> <mi>N</mi> <mi>V</mi> </mrow> </msub> </semantics></math> and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>C</mi> <mi>M</mi> </mrow> </msub> </semantics></math>; (<b>c</b>) <math display="inline"><semantics> <mrow> <mi>C</mi> <mi>L</mi> <mi>K</mi> </mrow> </semantics></math>; and (<b>d</b>) voltage difference between <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>E</mi> <mi>N</mi> <mi>V</mi> </mrow> </msub> </semantics></math> and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>C</mi> <mi>M</mi> </mrow> </msub> </semantics></math> during idle mode to reduce switching errors.</p>
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<p>Simulations of the proposed discrete PWM decoder showing: (<b>a</b>) “0010” repetitive <math display="inline"><semantics> <mrow> <mi>C</mi> <mi>L</mi> <mi>K</mi> </mrow> </semantics></math>, (<b>b</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>S</mi> <mi>K</mi> </mrow> </msub> </semantics></math> and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>R</mi> <mi>E</mi> <mi>F</mi> </mrow> </msub> </semantics></math>, and (<b>c</b>) recovered data <math display="inline"><semantics> <msub> <mi>V</mi> <mi>D</mi> </msub> </semantics></math>.</p>
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<p>Experimental work showing: (<b>a</b>) printed circuit, and (<b>b</b>) measurements setup.</p>
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<p>Waveform measurements obtained from oscilloscope showing: (<b>a</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>E</mi> <mi>H</mi> </mrow> </msub> </semantics></math> (red) and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>R</mi> <mi>E</mi> <mi>G</mi> </mrow> </msub> </semantics></math> (blue); (<b>b</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>C</mi> <mi>O</mi> <mi>M</mi> <mi>M</mi> </mrow> </msub> </semantics></math>; (<b>c</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>E</mi> <mi>N</mi> <mi>V</mi> </mrow> </msub> </semantics></math> (red) and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>C</mi> <mi>M</mi> </mrow> </msub> </semantics></math> (blue); (<b>d</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>S</mi> <mi>K</mi> </mrow> </msub> </semantics></math> (red) and <math display="inline"><semantics> <msub> <mi>V</mi> <mrow> <mi>R</mi> <mi>E</mi> <mi>F</mi> </mrow> </msub> </semantics></math> (blue); (<b>e</b>) <math display="inline"><semantics> <msub> <mi>V</mi> <mi>D</mi> </msub> </semantics></math> (red) and <math display="inline"><semantics> <mrow> <mi>C</mi> <mi>L</mi> <mi>K</mi> </mrow> </semantics></math> (blue); and (<b>f</b>) measured distance validation.</p>
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<p>A plot showing synchronization between <math display="inline"><semantics> <msub> <mi>V</mi> <mi>D</mi> </msub> </semantics></math> and <math display="inline"><semantics> <mrow> <mi>C</mi> <mi>L</mi> <mi>K</mi> </mrow> </semantics></math>, allowing data recovery and storage.</p>
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17 pages, 6717 KiB  
Article
An H-Bridge Switched Tank Converter with Reduced Inductance
by Xinxin Yang, Runquan Meng, Huajian Li, Jiahui Zhang, Xiang Bai and Ruishu Li
Electronics 2025, 14(3), 472; https://doi.org/10.3390/electronics14030472 - 24 Jan 2025
Viewed by 247
Abstract
Due to the restrictions of the operating environment and on-site space conditions, the energy routing devices used in Antarctic research stations must have a compact structure and require the internal power converter to have a high enough power density to reduce its size, [...] Read more.
Due to the restrictions of the operating environment and on-site space conditions, the energy routing devices used in Antarctic research stations must have a compact structure and require the internal power converter to have a high enough power density to reduce its size, so the internal DC/DC conversion link of the energy router adopts a two-stage voltage regulation scheme. In this paper, a Switched Tank Converter (STC) is used to realize the coarse voltage adjustment of the first stage. In order to further improve the power density of the STC, this paper integrates the half bridge with the same switching action in the STC, and several resonant slots share one inductor to obtain an H-bridge STC with reduced inductance. At the same time, an improved control method is proposed to solve the influence of passive device parameter error and the parasitic parameter on the resonant frequency by adjusting the on-time value of the switch on the rectifier side. This control method can effectively solve the influence of the passive device parameter difference on the converter without adding new devices, ensure the power density advantage of the converter, and improve efficiency. Finally, the validity and rationality of the circuit and the improved control method are verified by simulation and experiment. The experimental result shows that the H-bridge STC with reduced inductance has a power density of 1041 W/in3 at 600 W, which greatly improves the overall operating efficiency of the energy router. Full article
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<p>Switched Tank Converter topology.</p>
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<p>Traditional PWM control signal.</p>
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<p>H-bridge Switched Tank Converter (STC) topology.</p>
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<p>Equivalent circuit of H-bridge STC: (<b>a</b>) signal <span class="html-italic">Φ</span><sub>1</sub> control; (<b>b</b>) signal <span class="html-italic">Φ</span><sub>2</sub> control.</p>
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<p>Single-inductance H-bridge STC topology.</p>
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<p>Conventional PWM control and ideally inductor current waveform.</p>
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<p>Equivalent circuit of single-inductance H-bridge STC: (<b>a</b>) working mode 1; (<b>b</b>) working mode 2.</p>
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<p>Inductor current waveform under traditional control method.</p>
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<p>The improved control method and inductor current waveforms: (<b>a</b>) the improved control sequence; (<b>b</b>) the inductor current waveform under the improved control method.</p>
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<p>Comparison of total power loss of MOSFET.</p>
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<p>Inductor current simulation waveforms under traditional control method.</p>
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<p>Output voltage simulation waveform under traditional control method.</p>
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<p>Inductor current simulation waveform under improved control method.</p>
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<p>Output voltage simulation waveform under improved control method.</p>
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<p>Capacitor voltage simulation waveforms under improved control method.</p>
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<p>The experimental platform.</p>
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<p>Experimental circuit board: (<b>a</b>) single-inductance H-bridge STC hardware circuit board; (<b>b</b>) comparison of 3D PCB.</p>
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<p>Experimental waveform of inductor current under traditional control method.</p>
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<p>Experimental waveform of output voltage under traditional control.</p>
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<p>Experimental waveform of output voltage under improved control method.</p>
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<p>Experimental waveforms of resonant capacitor voltage and output voltage under improved control.</p>
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<p>Experimental waveforms of non-resonant capacitor voltage and output voltage under improved control.</p>
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23 pages, 6414 KiB  
Article
New Species of Byssosphaeria (Melanommataceae, Pleosporales) from the Mexican Tropical Montane Cloud Forest
by Aurora Cobos-Villagrán, Abigail Pérez-Valdespino, Ricardo Valenzuela, César Ramiro Martínez-González, Isolda Luna-Vega, Lourdes Villa-Tanaca, Aída Verónica Rodríguez-Tovar and Tania Raymundo
J. Fungi 2025, 11(2), 89; https://doi.org/10.3390/jof11020089 - 24 Jan 2025
Viewed by 372
Abstract
Byssosphaeria Cooke is a monophyletic genus of the family Melanommataceae. The genus is characterized by ascomata smaller than 1000 µm, globose, well-developed subiculum, with a flat ostiole, and yellow-orange or reddish-brown color around the ostiole. The peridium is composed of an external layer [...] Read more.
Byssosphaeria Cooke is a monophyletic genus of the family Melanommataceae. The genus is characterized by ascomata smaller than 1000 µm, globose, well-developed subiculum, with a flat ostiole, and yellow-orange or reddish-brown color around the ostiole. The peridium is composed of an external layer of irregular cells followed by an internal layer of thinner cells. Clavate asci have fusiform ascospores, a hyaline-to-brown color, with one or more septa. The genus Byssosphaeria is composed of 29 species: saprophytes, endophytes, and parasites of woody angiosperms, and they are found in wood, leaves, and other decaying substrates. The distribution of these species is cosmopolitan, and four species have been described in Mexico. This study describes, through morphological characteristics and the phylogenetic analysis of molecular markers (ITS, SSU, LSU, tef1-α), four new species of Byssosphaeria: B. bautistae, B. chrysostoma, B. neorhodomphala, and B. neoschiedermayriana. These species are saprophytes on wood rot and are distributed in mountainous mesophilic forests from the states of Hidalgo, Puebla, and Oaxaca. The significance of this study is in the diversity of this genus in Mexico since eight species have been described. Full article
(This article belongs to the Special Issue Ascomycota: Diversity, Taxonomy and Phylogeny, 2nd Edition)
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<p>Phylogenetic reconstruction based on the concatenated ITS, LSU, SSU, and <span class="html-italic">tef1-α</span> sequence alignment. Maximum parsimony and Bayesian analyses recovered identical topologies concerning the relationships among the main clades of <span class="html-italic">Byssosphaeria</span> members. For each node, the following values are provided: maximum parsimony (MP ≥ 70%, left)/maximum likelihood bootstrap (ML ≥ 70%, middle) and the Bayesian inference posterior probability (BIPP ≥ 0.85, right). The scale bar represents the expected number of nucleotide substitutions per site.</p>
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<p><span class="html-italic">Byssosphaeria bautistae</span> (T. Raymundo 6308, holotype). (<b>A</b>) Pseudothecia on the host surface/appearance of ascomata on the host; (<b>B</b>) close-up of pseudothecia and color around the ostiole; (<b>C</b>) longitudinal section of the pseudothecia and peridium; (<b>D</b>) asci; (<b>E</b>) ascospores with KOH; and (<b>F</b>) ascospores (phase-contrast).</p>
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<p><span class="html-italic">Byssosphaeria chrysostoma</span> (T. Raymundo 6221, holotype). (<b>A</b>) Pseudothecia on the host surface/appearance of ascomata on the host; (<b>B</b>) close-up of pseudothecia, color around the ostiole; (<b>C</b>) longitudinal section of the pseudothecia and peridium; (<b>D</b>) asci; (<b>E</b>) ascospores with KOH; and (<b>F</b>,<b>G</b>) ascospores (phase-contrast).</p>
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<p><span class="html-italic">Byssosphaeria neorhodomphala</span> (E. Escudero-Leyva 190, holotype). (<b>A</b>) Pseudothecia on the host surface/appearance of ascomata on the host; (<b>B</b>) close-up of pseudothecia, color around the ostiole; (<b>C</b>) longitudinal section of the pseudothecia and peridium; (<b>D</b>) asci; (<b>E</b>) ascospores with KOH; and (<b>F</b>) ascospores (phase-contrast).</p>
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<p><span class="html-italic">Byssosphaeria neoschiedermayriana</span> (R. Valenzuela 16092, holtype). (<b>A</b>) Pseudothecia on the host surface/appearance of ascomata on the host; (<b>B</b>) close-up of pseudothecia, color around the ostiole; (<b>C</b>) longitudinal section of the pseudothecia and peridium; (<b>D</b>) asci; (<b>E</b>) ascospores with KOH; and (<b>F</b>,<b>G</b>) ascospores (phase-contrast).</p>
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<p>Localities of the species of <span class="html-italic">Byssosphaeria</span> in Mexico.</p>
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23 pages, 1685 KiB  
Review
Crosstalk Between Abiotic and Biotic Stresses Responses and the Role of Chloroplast Retrograde Signaling in the Cross-Tolerance Phenomena in Plants
by Muhammad Kamran, Paweł Burdiak and Stanisław Karpiński
Cells 2025, 14(3), 176; https://doi.org/10.3390/cells14030176 - 23 Jan 2025
Viewed by 332
Abstract
In the natural environment, plants are simultaneously exposed to multivariable abiotic and biotic stresses. Typical abiotic stresses are changes in temperature, light intensity and quality, water stress (drought, flood), microelements availability, salinity, air pollutants, and others. Biotic stresses are caused by other organisms, [...] Read more.
In the natural environment, plants are simultaneously exposed to multivariable abiotic and biotic stresses. Typical abiotic stresses are changes in temperature, light intensity and quality, water stress (drought, flood), microelements availability, salinity, air pollutants, and others. Biotic stresses are caused by other organisms, such as pathogenic bacteria and viruses or parasites. This review presents the current state-of-the-art knowledge on programmed cell death in the cross-tolerance phenomena and its conditional molecular and physiological regulators, which simultaneously regulate plant acclimation, defense, and developmental responses. It highlights the role of the absorbed energy in excess and its dissipation as heat in the induction of the chloroplast retrograde phytohormonal, electrical, and reactive oxygen species signaling. It also discusses how systemic- and network-acquired acclimation and acquired systemic resistance are mutually regulated and demonstrates the role of non-photochemical quenching and the dissipation of absorbed energy in excess as heat in the cross-tolerance phenomenon. Finally, new evidence that plants evolved one molecular system to regulate cell death, acclimation, and cross-tolerance are presented and discussed. Full article
(This article belongs to the Section Cell Signaling)
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<p>Model of the chloroplast retrograde signaling pathways that regulate cell death (CD) and integrate immune defenses and plant acclimation responses—cross-tolerance to biotic and abiotic stresses. The red lighting-like symbol on the top demonstrates the absorption of energy in excess (AEE) required for electrical charge separation in P680. AEE induces the overproduction of electrons and protons, and thus in non-photochemical quenching (NPQ), heat, and electrical signaling waves. The excess of electrons leads to increased reactive oxygen species (ROS) production and a higher reduction in the plastoquinone (PQ) pool. This triggers redox changes in the stroma in ascorbate, glutathione, and other redox pair component pools, which regulate carbonic anhydrases (CA) activities, and thus, the CO<sub>2</sub>/O<sub>2</sub> ratio near RuBisCO and sugar production. This, in turn, triggers phytohormone precursor synthesis and photorespiration as a photosynthetic electron sink, which further increases ROS production in peroxisomes and mitochondria and regulates stomatal conductance and programmed cell death (PCD). Chloroplast stroma can be directly connected via stormless with the nucleus, and ES-, ROS-, heat-, and other-signaling molecules or dual transcription factors can be directly transduced to the nucleus and specifically alter nuclear-encoded gene expression and cross-tolerance to abiotic and biotic stresses. This happens in most foliar cells, but some cells induce PCD when the chloroplast outer membrane is disintegrated due to AEE, heat, salicylic acid (SA), and ethylene (ET) signaling. Red wavy-like and black lightning-like arrows show heat and electrical signaling waves, respectively. Solid lines show the confirmed regulatory signaling pathways, while dashed lines show hypothetical signaling pathways. Modified version from Karpiński and colleagues (2014) [<a href="#B11-cells-14-00176" class="html-bibr">11</a>] based on new data [<a href="#B15-cells-14-00176" class="html-bibr">15</a>,<a href="#B16-cells-14-00176" class="html-bibr">16</a>,<a href="#B17-cells-14-00176" class="html-bibr">17</a>,<a href="#B18-cells-14-00176" class="html-bibr">18</a>,<a href="#B19-cells-14-00176" class="html-bibr">19</a>,<a href="#B20-cells-14-00176" class="html-bibr">20</a>,<a href="#B21-cells-14-00176" class="html-bibr">21</a>,<a href="#B22-cells-14-00176" class="html-bibr">22</a>,<a href="#B23-cells-14-00176" class="html-bibr">23</a>,<a href="#B24-cells-14-00176" class="html-bibr">24</a>,<a href="#B41-cells-14-00176" class="html-bibr">41</a>,<a href="#B42-cells-14-00176" class="html-bibr">42</a>,<a href="#B78-cells-14-00176" class="html-bibr">78</a>,<a href="#B89-cells-14-00176" class="html-bibr">89</a>,<a href="#B90-cells-14-00176" class="html-bibr">90</a>,<a href="#B91-cells-14-00176" class="html-bibr">91</a>,<a href="#B92-cells-14-00176" class="html-bibr">92</a>,<a href="#B93-cells-14-00176" class="html-bibr">93</a>,<a href="#B94-cells-14-00176" class="html-bibr">94</a>,<a href="#B95-cells-14-00176" class="html-bibr">95</a>,<a href="#B96-cells-14-00176" class="html-bibr">96</a>].</p>
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<p>Systemic and network communication of non-photochemical quenching (NPQ) changes between photosystem II and mesophyll cells within and between plants. Electrical signaling (ES) and reactive oxygen species (ROS) waves can induce wavy-like changes in the NPQ value within a chloroplast, between all chloroplasts in the cell, in a whole leaf, in all leaves of a plant, and within the community-dwelling plants, such as the dandelion or <span class="html-italic">Arabidopsis</span>, when leaves of neighboring plants are in physical contact [<a href="#B18-cells-14-00176" class="html-bibr">18</a>,<a href="#B19-cells-14-00176" class="html-bibr">19</a>,<a href="#B20-cells-14-00176" class="html-bibr">20</a>,<a href="#B21-cells-14-00176" class="html-bibr">21</a>,<a href="#B22-cells-14-00176" class="html-bibr">22</a>,<a href="#B23-cells-14-00176" class="html-bibr">23</a>,<a href="#B24-cells-14-00176" class="html-bibr">24</a>]. ES and ROS waves transmitted from stressed cells across the whole plant and between plants regulate NPQ- and plastoquinone pool-dependent chloroplast retrograde signaling to induce systemic-acquired acclimation (SAA) (yellow-wavy arrows) in a plant and network-acquired acclimation (NAA) (red-wavy arrows) between plants. Physical contact and electrical conductivity (e.g., a drop of water or high relative humidity) are necessary for NAA. In both transmitter and receiver plants, ES causes spatiotemporal variations in energy quenching (NPQ) (solid black line), the following induction of the ROS wave (solid green line), and electrical signaling (ES) (solid blue line). The yellow lighting-like symbol indicates the stress stimuli. Water droplets show the humidity. Interdependent ion fluxes in the plants cause its variable amplitude. (Model modified from Szechyńska-Hebda et al. (2022) [<a href="#B23-cells-14-00176" class="html-bibr">23</a>]).</p>
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