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Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae

Botryosphaeriaceae are an important fungal family that cause woody plant diseases worldwide. Recent studies have established a correlation between environmental factors and disease expression; however, less is known about factors that trigger these diseases. The current study reports on the 43.3 Mb...

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Autores principales: Yan, Ji Ye, Zhao, Wen Sheng, Chen, Zhen, Xing, Qi Kai, Zhang, Wei, Chethana, K W Thilini, Xue, Min Feng, Xu, Jian Ping, Phillips, Alan J L, Wang, Yong, Liu, Jian Hua, Liu, Mei, Zhou, Ying, Jayawardena, Ruvishika S, Manawasinghe, Ishara S, Huang, Jin Bao, Qiao, Guang Hang, Fu, Chun Yuan, Guo, Fei Fei, Dissanayake, Asha J, Peng, You Liang, Hyde, Kevin D, Li, Xing Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824938/
https://www.ncbi.nlm.nih.gov/pubmed/29036669
http://dx.doi.org/10.1093/dnares/dsx040
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author Yan, Ji Ye
Zhao, Wen Sheng
Chen, Zhen
Xing, Qi Kai
Zhang, Wei
Chethana, K W Thilini
Xue, Min Feng
Xu, Jian Ping
Phillips, Alan J L
Wang, Yong
Liu, Jian Hua
Liu, Mei
Zhou, Ying
Jayawardena, Ruvishika S
Manawasinghe, Ishara S
Huang, Jin Bao
Qiao, Guang Hang
Fu, Chun Yuan
Guo, Fei Fei
Dissanayake, Asha J
Peng, You Liang
Hyde, Kevin D
Li, Xing Hong
author_facet Yan, Ji Ye
Zhao, Wen Sheng
Chen, Zhen
Xing, Qi Kai
Zhang, Wei
Chethana, K W Thilini
Xue, Min Feng
Xu, Jian Ping
Phillips, Alan J L
Wang, Yong
Liu, Jian Hua
Liu, Mei
Zhou, Ying
Jayawardena, Ruvishika S
Manawasinghe, Ishara S
Huang, Jin Bao
Qiao, Guang Hang
Fu, Chun Yuan
Guo, Fei Fei
Dissanayake, Asha J
Peng, You Liang
Hyde, Kevin D
Li, Xing Hong
author_sort Yan, Ji Ye
collection PubMed
description Botryosphaeriaceae are an important fungal family that cause woody plant diseases worldwide. Recent studies have established a correlation between environmental factors and disease expression; however, less is known about factors that trigger these diseases. The current study reports on the 43.3 Mb de novo genome of Lasiodiplodia theobromae and five other genomes of Botryosphaeriaceae pathogens. Botryosphaeriaceous genomes showed an expansion of gene families associated with cell wall degradation, nutrient uptake, secondary metabolism and membrane transport, which contribute to adaptations for wood degradation. Transcriptome analysis revealed that genes involved in carbohydrate catabolism, pectin, starch and sucrose metabolism, and pentose and glucuronate interconversion pathways were induced during infection. Furthermore, genes in carbohydrate-binding modules, lysine motif domain and the glycosyl hydrolase gene families were induced by high temperature. Among these genes, overexpression of two selected putative lignocellulase genes led to increased virulence in the transformants. These results demonstrate the importance of high temperatures in opportunistic infections. This study also presents a set of Botryosphaeriaceae-specific effectors responsible for the identification of virulence-related pathogen-associated molecular patterns and demonstrates their active participation in suppressing hypersensitive responses. Together, these findings significantly expand our understanding of the determinants of pathogenicity or virulence in Botryosphaeriaceae and provide new insights for developing management strategies against them.
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spelling pubmed-58249382018-02-28 Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae Yan, Ji Ye Zhao, Wen Sheng Chen, Zhen Xing, Qi Kai Zhang, Wei Chethana, K W Thilini Xue, Min Feng Xu, Jian Ping Phillips, Alan J L Wang, Yong Liu, Jian Hua Liu, Mei Zhou, Ying Jayawardena, Ruvishika S Manawasinghe, Ishara S Huang, Jin Bao Qiao, Guang Hang Fu, Chun Yuan Guo, Fei Fei Dissanayake, Asha J Peng, You Liang Hyde, Kevin D Li, Xing Hong DNA Res Full Papers Botryosphaeriaceae are an important fungal family that cause woody plant diseases worldwide. Recent studies have established a correlation between environmental factors and disease expression; however, less is known about factors that trigger these diseases. The current study reports on the 43.3 Mb de novo genome of Lasiodiplodia theobromae and five other genomes of Botryosphaeriaceae pathogens. Botryosphaeriaceous genomes showed an expansion of gene families associated with cell wall degradation, nutrient uptake, secondary metabolism and membrane transport, which contribute to adaptations for wood degradation. Transcriptome analysis revealed that genes involved in carbohydrate catabolism, pectin, starch and sucrose metabolism, and pentose and glucuronate interconversion pathways were induced during infection. Furthermore, genes in carbohydrate-binding modules, lysine motif domain and the glycosyl hydrolase gene families were induced by high temperature. Among these genes, overexpression of two selected putative lignocellulase genes led to increased virulence in the transformants. These results demonstrate the importance of high temperatures in opportunistic infections. This study also presents a set of Botryosphaeriaceae-specific effectors responsible for the identification of virulence-related pathogen-associated molecular patterns and demonstrates their active participation in suppressing hypersensitive responses. Together, these findings significantly expand our understanding of the determinants of pathogenicity or virulence in Botryosphaeriaceae and provide new insights for developing management strategies against them. Oxford University Press 2018-02 2017-10-03 /pmc/articles/PMC5824938/ /pubmed/29036669 http://dx.doi.org/10.1093/dnares/dsx040 Text en © The Author 2017. 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
Yan, Ji Ye
Zhao, Wen Sheng
Chen, Zhen
Xing, Qi Kai
Zhang, Wei
Chethana, K W Thilini
Xue, Min Feng
Xu, Jian Ping
Phillips, Alan J L
Wang, Yong
Liu, Jian Hua
Liu, Mei
Zhou, Ying
Jayawardena, Ruvishika S
Manawasinghe, Ishara S
Huang, Jin Bao
Qiao, Guang Hang
Fu, Chun Yuan
Guo, Fei Fei
Dissanayake, Asha J
Peng, You Liang
Hyde, Kevin D
Li, Xing Hong
Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title_full Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title_fullStr Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title_full_unstemmed Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title_short Comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of Botryosphaeriaceae
title_sort comparative genome and transcriptome analyses reveal adaptations to opportunistic infections in woody plant degrading pathogens of botryosphaeriaceae
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824938/
https://www.ncbi.nlm.nih.gov/pubmed/29036669
http://dx.doi.org/10.1093/dnares/dsx040
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