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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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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. |
format | Online Article Text |
id | pubmed-6014366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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