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Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes

Obligate intracellular pathogens depend on their host for growth yet must also evade detection by host defenses. Here we investigate host adaptation in two Microsporidia, the specialist Edhazardia aedis and the generalist Vavraia culicis, pathogens of disease vector mosquitoes. Genomic analysis and...

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Autores principales: Desjardins, Christopher A., Sanscrainte, Neil D., Goldberg, Jonathan M., Heiman, David, Young, Sarah, Zeng, Qiandong, Madhani, Hiten D., Becnel, James J., Cuomo, Christina A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435813/
https://www.ncbi.nlm.nih.gov/pubmed/25968466
http://dx.doi.org/10.1038/ncomms8121
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author Desjardins, Christopher A.
Sanscrainte, Neil D.
Goldberg, Jonathan M.
Heiman, David
Young, Sarah
Zeng, Qiandong
Madhani, Hiten D.
Becnel, James J.
Cuomo, Christina A
author_facet Desjardins, Christopher A.
Sanscrainte, Neil D.
Goldberg, Jonathan M.
Heiman, David
Young, Sarah
Zeng, Qiandong
Madhani, Hiten D.
Becnel, James J.
Cuomo, Christina A
author_sort Desjardins, Christopher A.
collection PubMed
description Obligate intracellular pathogens depend on their host for growth yet must also evade detection by host defenses. Here we investigate host adaptation in two Microsporidia, the specialist Edhazardia aedis and the generalist Vavraia culicis, pathogens of disease vector mosquitoes. Genomic analysis and deep RNA-Seq across infection time courses reveal fundamental differences between these pathogens. E. aedis retains enhanced cell surface modification and signalling capacity, upregulating protein trafficking and secretion dynamically during infection. V. culicis is less dependent on its host for basic metabolites and retains a subset of spliceosomal components, with a transcriptome broadly focused on growth and replication. Transcriptional profiling of mosquito immune responses reveals that response to infection by E. aedis differs dramatically depending on the mode of infection, and that antimicrobial defensins may play a general role in mosquito defense against Microsporidia. This analysis illuminates fundamentally different evolutionary paths and host interplay of specialist and generalist pathogens.
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spelling pubmed-44358132015-06-29 Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes Desjardins, Christopher A. Sanscrainte, Neil D. Goldberg, Jonathan M. Heiman, David Young, Sarah Zeng, Qiandong Madhani, Hiten D. Becnel, James J. Cuomo, Christina A Nat Commun Article Obligate intracellular pathogens depend on their host for growth yet must also evade detection by host defenses. Here we investigate host adaptation in two Microsporidia, the specialist Edhazardia aedis and the generalist Vavraia culicis, pathogens of disease vector mosquitoes. Genomic analysis and deep RNA-Seq across infection time courses reveal fundamental differences between these pathogens. E. aedis retains enhanced cell surface modification and signalling capacity, upregulating protein trafficking and secretion dynamically during infection. V. culicis is less dependent on its host for basic metabolites and retains a subset of spliceosomal components, with a transcriptome broadly focused on growth and replication. Transcriptional profiling of mosquito immune responses reveals that response to infection by E. aedis differs dramatically depending on the mode of infection, and that antimicrobial defensins may play a general role in mosquito defense against Microsporidia. This analysis illuminates fundamentally different evolutionary paths and host interplay of specialist and generalist pathogens. Nature Pub. Group 2015-05-13 /pmc/articles/PMC4435813/ /pubmed/25968466 http://dx.doi.org/10.1038/ncomms8121 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Desjardins, Christopher A.
Sanscrainte, Neil D.
Goldberg, Jonathan M.
Heiman, David
Young, Sarah
Zeng, Qiandong
Madhani, Hiten D.
Becnel, James J.
Cuomo, Christina A
Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title_full Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title_fullStr Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title_full_unstemmed Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title_short Contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
title_sort contrasting host–pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435813/
https://www.ncbi.nlm.nih.gov/pubmed/25968466
http://dx.doi.org/10.1038/ncomms8121
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