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High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits

Animals are under constant selective pressure from a myriad of diverse pathogens. Microsporidia are ubiquitous animal parasites, but the influence they exert on shaping animal genomes is mostly unknown. Using multiplexed competition assays, we measured the impact of four different species of microsp...

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Autores principales: Mok, Calvin, Xiao, Meng A., Wan, Yin C., Zhao, Winnie, Ahmed, Shanzeh M., Luallen, Robert J., Reinke, Aaron W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030041/
https://www.ncbi.nlm.nih.gov/pubmed/36893187
http://dx.doi.org/10.1371/journal.ppat.1011225
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author Mok, Calvin
Xiao, Meng A.
Wan, Yin C.
Zhao, Winnie
Ahmed, Shanzeh M.
Luallen, Robert J.
Reinke, Aaron W.
author_facet Mok, Calvin
Xiao, Meng A.
Wan, Yin C.
Zhao, Winnie
Ahmed, Shanzeh M.
Luallen, Robert J.
Reinke, Aaron W.
author_sort Mok, Calvin
collection PubMed
description Animals are under constant selective pressure from a myriad of diverse pathogens. Microsporidia are ubiquitous animal parasites, but the influence they exert on shaping animal genomes is mostly unknown. Using multiplexed competition assays, we measured the impact of four different species of microsporidia on 22 wild isolates of Caenorhabditis elegans. This resulted in the identification and confirmation of 13 strains with significantly altered population fitness profiles under infection conditions. One of these identified strains, JU1400, is sensitive to an epidermal-infecting species by lacking tolerance to infection. JU1400 is also resistant to an intestinal-infecting species and can specifically recognize and destroy this pathogen. Genetic mapping of JU1400 demonstrates that these two opposing phenotypes are caused by separate loci. Transcriptional analysis reveals the JU1400 sensitivity to epidermal microsporidia infection results in a response pattern that shares similarity to toxin-induced responses. In contrast, we do not observe JU1400 intestinal resistance being regulated at the transcriptional level. The transcriptional response to these four microsporidia species is conserved, with C. elegans strain-specific differences in potential immune genes. Together, our results show that phenotypic differences to microsporidia infection amongst C. elegans are common and that animals can evolve species-specific genetic interactions.
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spelling pubmed-100300412023-03-22 High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits Mok, Calvin Xiao, Meng A. Wan, Yin C. Zhao, Winnie Ahmed, Shanzeh M. Luallen, Robert J. Reinke, Aaron W. PLoS Pathog Research Article Animals are under constant selective pressure from a myriad of diverse pathogens. Microsporidia are ubiquitous animal parasites, but the influence they exert on shaping animal genomes is mostly unknown. Using multiplexed competition assays, we measured the impact of four different species of microsporidia on 22 wild isolates of Caenorhabditis elegans. This resulted in the identification and confirmation of 13 strains with significantly altered population fitness profiles under infection conditions. One of these identified strains, JU1400, is sensitive to an epidermal-infecting species by lacking tolerance to infection. JU1400 is also resistant to an intestinal-infecting species and can specifically recognize and destroy this pathogen. Genetic mapping of JU1400 demonstrates that these two opposing phenotypes are caused by separate loci. Transcriptional analysis reveals the JU1400 sensitivity to epidermal microsporidia infection results in a response pattern that shares similarity to toxin-induced responses. In contrast, we do not observe JU1400 intestinal resistance being regulated at the transcriptional level. The transcriptional response to these four microsporidia species is conserved, with C. elegans strain-specific differences in potential immune genes. Together, our results show that phenotypic differences to microsporidia infection amongst C. elegans are common and that animals can evolve species-specific genetic interactions. Public Library of Science 2023-03-09 /pmc/articles/PMC10030041/ /pubmed/36893187 http://dx.doi.org/10.1371/journal.ppat.1011225 Text en © 2023 Mok et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mok, Calvin
Xiao, Meng A.
Wan, Yin C.
Zhao, Winnie
Ahmed, Shanzeh M.
Luallen, Robert J.
Reinke, Aaron W.
High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title_full High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title_fullStr High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title_full_unstemmed High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title_short High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits
title_sort high-throughput phenotyping of infection by diverse microsporidia species reveals a wild c. elegans strain with opposing resistance and susceptibility traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030041/
https://www.ncbi.nlm.nih.gov/pubmed/36893187
http://dx.doi.org/10.1371/journal.ppat.1011225
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