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Widespread signatures of selection for secreted peptidases in a fungal plant pathogen
BACKGROUND: Fungal plant pathogens secrete a large arsenal of hydrolytic enzymes during the course of infection, including peptidases. Secreted peptidases have been extensively studied for their role as effectors. In this study, we combined transcriptomics, comparative genomics and evolutionary anal...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784588/ https://www.ncbi.nlm.nih.gov/pubmed/29368587 http://dx.doi.org/10.1186/s12862-018-1123-3 |
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author | Krishnan, Parvathy Ma, Xin McDonald, Bruce A. Brunner, Patrick C. |
author_facet | Krishnan, Parvathy Ma, Xin McDonald, Bruce A. Brunner, Patrick C. |
author_sort | Krishnan, Parvathy |
collection | PubMed |
description | BACKGROUND: Fungal plant pathogens secrete a large arsenal of hydrolytic enzymes during the course of infection, including peptidases. Secreted peptidases have been extensively studied for their role as effectors. In this study, we combined transcriptomics, comparative genomics and evolutionary analyses to investigate all 39 secreted peptidases in the fungal wheat pathogen Zymoseptoria tritici and its close relatives Z. pseudotritici and Z. ardabiliae. RESULTS: RNA-seq data revealed that a majority of the secreted peptidases displayed differential transcription during the course of Z. tritici infection, indicative of specialization for different stages in the life cycle. Evolutionary analyses detected widespread evidence of adaptive evolution acting on at least 28 of the peptidases. A few peptidases displayed lineage-specific rates of molecular evolution, suggesting altered selection pressure in Z. tritici following host specialization on domesticated wheat. The peptidases belonging to MEROPS families A1 and G1 emerged as a particularly interesting group that may play key roles in host-pathogen co-evolution, host adaptation and pathogenicity. Sister genes in the A1 and G1 families showed accelerated substitution rates after gene duplications. CONCLUSIONS: These results suggest widespread evolution of secreted peptidases leading to novel gene functions, consistent with predicted models of “escape from adaptive conflict” and “neo-functionalization”. Our analyses identified candidate genes worthy of functional analyses that may encode effector functions, for example by suppressing plant defenses during the biotrophic phase of infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1123-3) contains suppl ementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5784588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57845882018-02-07 Widespread signatures of selection for secreted peptidases in a fungal plant pathogen Krishnan, Parvathy Ma, Xin McDonald, Bruce A. Brunner, Patrick C. BMC Evol Biol Research Article BACKGROUND: Fungal plant pathogens secrete a large arsenal of hydrolytic enzymes during the course of infection, including peptidases. Secreted peptidases have been extensively studied for their role as effectors. In this study, we combined transcriptomics, comparative genomics and evolutionary analyses to investigate all 39 secreted peptidases in the fungal wheat pathogen Zymoseptoria tritici and its close relatives Z. pseudotritici and Z. ardabiliae. RESULTS: RNA-seq data revealed that a majority of the secreted peptidases displayed differential transcription during the course of Z. tritici infection, indicative of specialization for different stages in the life cycle. Evolutionary analyses detected widespread evidence of adaptive evolution acting on at least 28 of the peptidases. A few peptidases displayed lineage-specific rates of molecular evolution, suggesting altered selection pressure in Z. tritici following host specialization on domesticated wheat. The peptidases belonging to MEROPS families A1 and G1 emerged as a particularly interesting group that may play key roles in host-pathogen co-evolution, host adaptation and pathogenicity. Sister genes in the A1 and G1 families showed accelerated substitution rates after gene duplications. CONCLUSIONS: These results suggest widespread evolution of secreted peptidases leading to novel gene functions, consistent with predicted models of “escape from adaptive conflict” and “neo-functionalization”. Our analyses identified candidate genes worthy of functional analyses that may encode effector functions, for example by suppressing plant defenses during the biotrophic phase of infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1123-3) contains suppl ementary material, which is available to authorized users. BioMed Central 2018-01-24 /pmc/articles/PMC5784588/ /pubmed/29368587 http://dx.doi.org/10.1186/s12862-018-1123-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Krishnan, Parvathy Ma, Xin McDonald, Bruce A. Brunner, Patrick C. Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title | Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title_full | Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title_fullStr | Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title_full_unstemmed | Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title_short | Widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
title_sort | widespread signatures of selection for secreted peptidases in a fungal plant pathogen |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784588/ https://www.ncbi.nlm.nih.gov/pubmed/29368587 http://dx.doi.org/10.1186/s12862-018-1123-3 |
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