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Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali
Horizontal gene transfer (HGT) often has strong benefits for fungi. In a study of samples from apple canker in Shaanxi Province, China, diverse microbes, along with the necrotrophic pathogen Valsa mali, were found to colonize the apple bark, thus providing ample opportunity for HGT to occur. In the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025739/ https://www.ncbi.nlm.nih.gov/pubmed/27634406 http://dx.doi.org/10.1038/srep33129 |
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author | Yin, Zhiyuan Zhu, Baitao Feng, Hao Huang, Lili |
author_facet | Yin, Zhiyuan Zhu, Baitao Feng, Hao Huang, Lili |
author_sort | Yin, Zhiyuan |
collection | PubMed |
description | Horizontal gene transfer (HGT) often has strong benefits for fungi. In a study of samples from apple canker in Shaanxi Province, China, diverse microbes, along with the necrotrophic pathogen Valsa mali, were found to colonize the apple bark, thus providing ample opportunity for HGT to occur. In the present study, we identified 32 HGT events in V. mali by combining phyletic distribution-based methods with phylogenetic analyses. Most of these HGTs were from bacteria, whereas several others were from eukaryotes. Three HGTs putatively functioned in competition with actinomycetes, some of which showed a significant inhibitory effect on V. mali. Three HGTs that were probably involved in nitrogen uptake were also identified. Ten HGTs were thought to be involved in pathogenicity because they were related to known virulence factors, including cell wall-degrading enzymes and candidate effector proteins. HGT14, together with HGT32, was shown to contribute to bleomycin resistance of V. mali.These results suggest that HGT drives the adaptive evolution of V. mali. The HGTs identified here provide new clues for unveiling the adaptation mechanisms and virulence determinants of V. mali. |
format | Online Article Text |
id | pubmed-5025739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50257392016-09-22 Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali Yin, Zhiyuan Zhu, Baitao Feng, Hao Huang, Lili Sci Rep Article Horizontal gene transfer (HGT) often has strong benefits for fungi. In a study of samples from apple canker in Shaanxi Province, China, diverse microbes, along with the necrotrophic pathogen Valsa mali, were found to colonize the apple bark, thus providing ample opportunity for HGT to occur. In the present study, we identified 32 HGT events in V. mali by combining phyletic distribution-based methods with phylogenetic analyses. Most of these HGTs were from bacteria, whereas several others were from eukaryotes. Three HGTs putatively functioned in competition with actinomycetes, some of which showed a significant inhibitory effect on V. mali. Three HGTs that were probably involved in nitrogen uptake were also identified. Ten HGTs were thought to be involved in pathogenicity because they were related to known virulence factors, including cell wall-degrading enzymes and candidate effector proteins. HGT14, together with HGT32, was shown to contribute to bleomycin resistance of V. mali.These results suggest that HGT drives the adaptive evolution of V. mali. The HGTs identified here provide new clues for unveiling the adaptation mechanisms and virulence determinants of V. mali. Nature Publishing Group 2016-09-16 /pmc/articles/PMC5025739/ /pubmed/27634406 http://dx.doi.org/10.1038/srep33129 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yin, Zhiyuan Zhu, Baitao Feng, Hao Huang, Lili Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title | Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title_full | Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title_fullStr | Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title_full_unstemmed | Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title_short | Horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen Valsa mali |
title_sort | horizontal gene transfer drives adaptive colonization of apple trees by the fungal pathogen valsa mali |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025739/ https://www.ncbi.nlm.nih.gov/pubmed/27634406 http://dx.doi.org/10.1038/srep33129 |
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