Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal
ABSTRACT 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...
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American Society for Microbiology
2017
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oai:doaj.org-article:95eac1b72a354c4f81312915e6dcf1172021-11-15T15:21:52ZGenomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal10.1128/mSphere.00408-172379-5042https://doaj.org/article/95eac1b72a354c4f81312915e6dcf1172017-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00408-17https://doaj.org/toc/2379-5042ABSTRACT 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.Jamie McGowanDavid A. FitzpatrickAmerican Society for Microbiologyarticlecomparative genomicseffectorsevolutionoomycotasecretomesimilarity networkMicrobiologyQR1-502ENmSphere, Vol 2, Iss 6 (2017) |
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comparative genomics effectors evolution oomycota secretome similarity network Microbiology QR1-502 |
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comparative genomics effectors evolution oomycota secretome similarity network Microbiology QR1-502 Jamie McGowan David A. Fitzpatrick Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal |
description |
ABSTRACT 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 |
article |
author |
Jamie McGowan David A. Fitzpatrick |
author_facet |
Jamie McGowan David A. Fitzpatrick |
author_sort |
Jamie McGowan |
title |
Genomic, Network, and Phylogenetic Analysis of the Oomycete Effector Arsenal |
title_short |
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_sort |
genomic, network, and phylogenetic analysis of the oomycete effector arsenal |
publisher |
American Society for Microbiology |
publishDate |
2017 |
url |
https://doaj.org/article/95eac1b72a354c4f81312915e6dcf117 |
work_keys_str_mv |
AT jamiemcgowan genomicnetworkandphylogeneticanalysisoftheoomyceteeffectorarsenal AT davidafitzpatrick genomicnetworkandphylogeneticanalysisoftheoomyceteeffectorarsenal |
_version_ |
1718428085482684416 |