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Comparative genomic analyses reveal the features for adaptation to nematodes in fungi

Nematophagous (NP) fungi are ecologically important components of the soil microbiome in natural ecosystems. Esteya vermicola (Ev) has been reported as a NP fungus with a poorly understood evolutionary history and mechanism of adaptation to parasitism. Furthermore, NP fungal genomic basis of lifesty...

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Autores principales: Wang, Ruizhen, Dong, Leiming, He, Ran, Wang, Qinghua, Chen, Yuequ, Qu, Liangjian, Zhang, Yong-An
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014366/
https://www.ncbi.nlm.nih.gov/pubmed/29315395
http://dx.doi.org/10.1093/dnares/dsx053
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author Wang, Ruizhen
Dong, Leiming
He, Ran
Wang, Qinghua
Chen, Yuequ
Qu, Liangjian
Zhang, Yong-An
author_facet Wang, Ruizhen
Dong, Leiming
He, Ran
Wang, Qinghua
Chen, Yuequ
Qu, Liangjian
Zhang, Yong-An
author_sort Wang, Ruizhen
collection PubMed
description Nematophagous (NP) fungi are ecologically important components of the soil microbiome in natural ecosystems. Esteya vermicola (Ev) has been reported as a NP fungus with a poorly understood evolutionary history and mechanism of adaptation to parasitism. Furthermore, NP fungal genomic basis of lifestyle was still unclear. We sequenced and annotated the Ev genome (34.2 Mbp) and integrated genetic makeup and evolution of pathogenic genes to investigate NP fungi. The results revealed that NP fungi had some abundant pathogenic genes corresponding to their niche. A number of gene families involved in pathogenicity were expanded, and some pathogenic orthologous genes underwent positive selection. NP fungi with diverse morphological features exhibit similarities of evolutionary convergence in attacking nematodes, but their genetic makeup and microscopic mechanism are different. Endoparasitic NP fungi showed similarity in large number of transporters and secondary metabolite coding genes. Noteworthy, expanded families of transporters and endo-beta-glucanase implied great genetic potential of Ev in quickly perturbing nematode metabolism and parasitic behavior. These results facilitate our understanding of NP fungal genomic features for adaptation to nematodes and lay a solid theoretical foundation for further research and application.
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spelling pubmed-60143662018-06-27 Comparative genomic analyses reveal the features for adaptation to nematodes in fungi Wang, Ruizhen Dong, Leiming He, Ran Wang, Qinghua Chen, Yuequ Qu, Liangjian Zhang, Yong-An DNA Res Full Papers Nematophagous (NP) fungi are ecologically important components of the soil microbiome in natural ecosystems. Esteya vermicola (Ev) has been reported as a NP fungus with a poorly understood evolutionary history and mechanism of adaptation to parasitism. Furthermore, NP fungal genomic basis of lifestyle was still unclear. We sequenced and annotated the Ev genome (34.2 Mbp) and integrated genetic makeup and evolution of pathogenic genes to investigate NP fungi. The results revealed that NP fungi had some abundant pathogenic genes corresponding to their niche. A number of gene families involved in pathogenicity were expanded, and some pathogenic orthologous genes underwent positive selection. NP fungi with diverse morphological features exhibit similarities of evolutionary convergence in attacking nematodes, but their genetic makeup and microscopic mechanism are different. Endoparasitic NP fungi showed similarity in large number of transporters and secondary metabolite coding genes. Noteworthy, expanded families of transporters and endo-beta-glucanase implied great genetic potential of Ev in quickly perturbing nematode metabolism and parasitic behavior. These results facilitate our understanding of NP fungal genomic features for adaptation to nematodes and lay a solid theoretical foundation for further research and application. Oxford University Press 2018-06 2018-01-05 /pmc/articles/PMC6014366/ /pubmed/29315395 http://dx.doi.org/10.1093/dnares/dsx053 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Wang, Ruizhen
Dong, Leiming
He, Ran
Wang, Qinghua
Chen, Yuequ
Qu, Liangjian
Zhang, Yong-An
Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title_full Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title_fullStr Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title_full_unstemmed Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title_short Comparative genomic analyses reveal the features for adaptation to nematodes in fungi
title_sort comparative genomic analyses reveal the features for adaptation to nematodes in fungi
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014366/
https://www.ncbi.nlm.nih.gov/pubmed/29315395
http://dx.doi.org/10.1093/dnares/dsx053
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