Cargando…

Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal

The oomycetes are a class of microscopic, filamentous eukaryotes within the stramenopiles-alveolate-Rhizaria (SAR) supergroup and include ecologically significant animal and plant pathogens. Oomycetes secrete large arsenals of effector proteins that degrade host cell components, manipulate host immu...

Descripción completa

Detalles Bibliográficos
Autores principales: McGowan, Jamie, Fitzpatrick, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700374/
https://www.ncbi.nlm.nih.gov/pubmed/29202039
http://dx.doi.org/10.1128/mSphere.00408-17
_version_ 1783281109804515328
author McGowan, Jamie
Fitzpatrick, David A.
author_facet McGowan, Jamie
Fitzpatrick, David A.
author_sort McGowan, Jamie
collection PubMed
description The oomycetes are a class of microscopic, filamentous eukaryotes within the stramenopiles-alveolate-Rhizaria (SAR) supergroup and include ecologically significant animal and plant pathogens. Oomycetes secrete large arsenals of effector proteins that degrade host cell components, manipulate host immune responses, and induce necrosis, enabling parasitic colonization. This study investigated the expansion and evolution of effectors in 37 oomycete species in 4 oomycete orders, including Albuginales, Peronosporales, Pythiales, and Saprolegniales species. Our results highlight the large expansions of effector protein families, including glycoside hydrolases, pectinases, and necrosis-inducing proteins, in Phytophthora species. Species-specific expansions, including expansions of chitinases in Aphanomyces astaci and Pythium oligandrum, were detected. Novel effectors which may be involved in suppressing animal immune responses in Ap. astaci and Py. insidiosum were also identified. Type 2 necrosis-inducing proteins with an unusual phylogenetic history were also located in a number of oomycete species. We also investigated the "RxLR" effector complement of all 37 species and, as expected, observed large expansions in Phytophthora species numbers. Our results provide in-depth sequence information on all putative RxLR effectors from all 37 species. This work represents an up-to-date in silico catalogue of the effector arsenal of the oomycetes based on the 37 genomes currently available. IMPORTANCE The oomycetes are a class of microscopic, filamentous eukaryotes and include ecologically significant animal and plant pathogens. Oomycetes secrete large arsenals of effector proteins that degrade host cell components, manipulate host immune responses, and induce necrosis, enabling parasitic colonization. In this study, we catalogued the number and evolution of effectors in 37 oomycete species whose genomes have been completely sequenced. Large expansions of effector protein families in Phytophthora species, including glycoside hydrolases, pectinases, and necrosis-inducing proteins, were observed. Species-specific expansions were detected, including chitinases in Aphanomyces astaci and Pythium oligandrum. Novel effectors which may be involved in suppressing animal immune responses were identified in Ap. astaci and Py. oligandrum. Type 2 necrosis-inducing proteins with an unusual phylogenetic history were also located. This work represents an up-to-date in silico catalogue of the effector arsenal of the oomycetes based on the 37 genomes currently available.
format Online
Article
Text
id pubmed-5700374
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-57003742017-12-01 Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal McGowan, Jamie Fitzpatrick, David A. mSphere Research Article The oomycetes are a class of microscopic, filamentous eukaryotes within the stramenopiles-alveolate-Rhizaria (SAR) supergroup and include ecologically significant animal and plant pathogens. Oomycetes secrete large arsenals of effector proteins that degrade host cell components, manipulate host immune responses, and induce necrosis, enabling parasitic colonization. This study investigated the expansion and evolution of effectors in 37 oomycete species in 4 oomycete orders, including Albuginales, Peronosporales, Pythiales, and Saprolegniales species. Our results highlight the large expansions of effector protein families, including glycoside hydrolases, pectinases, and necrosis-inducing proteins, in Phytophthora species. Species-specific expansions, including expansions of chitinases in Aphanomyces astaci and Pythium oligandrum, were detected. Novel effectors which may be involved in suppressing animal immune responses in Ap. astaci and Py. insidiosum were also identified. Type 2 necrosis-inducing proteins with an unusual phylogenetic history were also located in a number of oomycete species. We also investigated the "RxLR" effector complement of all 37 species and, as expected, observed large expansions in Phytophthora species numbers. Our results provide in-depth sequence information on all putative RxLR effectors from all 37 species. This work represents an up-to-date in silico catalogue of the effector arsenal of the oomycetes based on the 37 genomes currently available. IMPORTANCE The oomycetes are a class of microscopic, filamentous eukaryotes and include ecologically significant animal and plant pathogens. Oomycetes secrete large arsenals of effector proteins that degrade host cell components, manipulate host immune responses, and induce necrosis, enabling parasitic colonization. In this study, we catalogued the number and evolution of effectors in 37 oomycete species whose genomes have been completely sequenced. Large expansions of effector protein families in Phytophthora species, including glycoside hydrolases, pectinases, and necrosis-inducing proteins, were observed. Species-specific expansions were detected, including chitinases in Aphanomyces astaci and Pythium oligandrum. Novel effectors which may be involved in suppressing animal immune responses were identified in Ap. astaci and Py. oligandrum. Type 2 necrosis-inducing proteins with an unusual phylogenetic history were also located. This work represents an up-to-date in silico catalogue of the effector arsenal of the oomycetes based on the 37 genomes currently available. American Society for Microbiology 2017-11-22 /pmc/articles/PMC5700374/ /pubmed/29202039 http://dx.doi.org/10.1128/mSphere.00408-17 Text en Copyright © 2017 McGowan and Fitzpatrick. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
McGowan, Jamie
Fitzpatrick, David A.
Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title_full Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title_fullStr Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title_full_unstemmed Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title_short Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
title_sort genomic, network, and phylogenetic analysis of the oomycete effector arsenal
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700374/
https://www.ncbi.nlm.nih.gov/pubmed/29202039
http://dx.doi.org/10.1128/mSphere.00408-17
work_keys_str_mv AT mcgowanjamie genomicnetworkandphylogeneticanalysisoftheoomyceteeffectorarsenal
AT fitzpatrickdavida genomicnetworkandphylogeneticanalysisoftheoomyceteeffectorarsenal