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Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors

Most plant viruses are vectored by insects and the interactions of virus-plant-vector have important ecological and evolutionary implications. Insect vectors often perform better on virus-infected plants. This indirect mutualism between plant viruses and insect vectors promotes the spread of virus a...

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Autores principales: Li, Ping, Liu, Chao, Deng, Wen-Hao, Yao, Dan-Mei, Pan, Li-Long, Li, Yun-Qin, Liu, Yin-Quan, Liang, Yan, Zhou, Xue-Ping, Wang, Xiao-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400417/
https://www.ncbi.nlm.nih.gov/pubmed/30789967
http://dx.doi.org/10.1371/journal.ppat.1007607
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author Li, Ping
Liu, Chao
Deng, Wen-Hao
Yao, Dan-Mei
Pan, Li-Long
Li, Yun-Qin
Liu, Yin-Quan
Liang, Yan
Zhou, Xue-Ping
Wang, Xiao-Wei
author_facet Li, Ping
Liu, Chao
Deng, Wen-Hao
Yao, Dan-Mei
Pan, Li-Long
Li, Yun-Qin
Liu, Yin-Quan
Liang, Yan
Zhou, Xue-Ping
Wang, Xiao-Wei
author_sort Li, Ping
collection PubMed
description Most plant viruses are vectored by insects and the interactions of virus-plant-vector have important ecological and evolutionary implications. Insect vectors often perform better on virus-infected plants. This indirect mutualism between plant viruses and insect vectors promotes the spread of virus and has significant agronomical effects. However, few studies have investigated how plant viruses manipulate plant defenses and promote vector performance. Begomoviruses are a prominent group of plant viruses in tropical and sub-tropical agro-ecosystems and are transmitted by whiteflies. Working with the whitefly Bemisia tabaci, begomoviruses and tobacco, we revealed that C2 protein of begomoviruses lacking DNA satellites was responsible for the suppression of plant defenses against whitefly vectors. We found that infection of plants by tomato yellow leaf curl virus (TYLCV), one of the most devastating begomoviruses worldwide, promoted the survival and reproduction of whitefly vectors. TYLCV C2 protein suppressed plant defenses by interacting with plant ubiquitin. This interaction compromised the degradation of JAZ1 protein, thus inhibiting jasmonic acid defense and the expression of MYC2-regulated terpene synthase genes. We further demonstrated that function of C2 protein among begomoviruses not associated with satellites is well conserved and ubiquitination is an evolutionarily conserved target of begomoviruses for the suppression of plant resistance to whitefly vectors. Taken together, these results demonstrate that ubiquitination inhibition by begomovirus C2 protein might be a general mechanism in begomovirus, whitefly and plant interactions.
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spelling pubmed-64004172019-03-17 Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors Li, Ping Liu, Chao Deng, Wen-Hao Yao, Dan-Mei Pan, Li-Long Li, Yun-Qin Liu, Yin-Quan Liang, Yan Zhou, Xue-Ping Wang, Xiao-Wei PLoS Pathog Research Article Most plant viruses are vectored by insects and the interactions of virus-plant-vector have important ecological and evolutionary implications. Insect vectors often perform better on virus-infected plants. This indirect mutualism between plant viruses and insect vectors promotes the spread of virus and has significant agronomical effects. However, few studies have investigated how plant viruses manipulate plant defenses and promote vector performance. Begomoviruses are a prominent group of plant viruses in tropical and sub-tropical agro-ecosystems and are transmitted by whiteflies. Working with the whitefly Bemisia tabaci, begomoviruses and tobacco, we revealed that C2 protein of begomoviruses lacking DNA satellites was responsible for the suppression of plant defenses against whitefly vectors. We found that infection of plants by tomato yellow leaf curl virus (TYLCV), one of the most devastating begomoviruses worldwide, promoted the survival and reproduction of whitefly vectors. TYLCV C2 protein suppressed plant defenses by interacting with plant ubiquitin. This interaction compromised the degradation of JAZ1 protein, thus inhibiting jasmonic acid defense and the expression of MYC2-regulated terpene synthase genes. We further demonstrated that function of C2 protein among begomoviruses not associated with satellites is well conserved and ubiquitination is an evolutionarily conserved target of begomoviruses for the suppression of plant resistance to whitefly vectors. Taken together, these results demonstrate that ubiquitination inhibition by begomovirus C2 protein might be a general mechanism in begomovirus, whitefly and plant interactions. Public Library of Science 2019-02-21 /pmc/articles/PMC6400417/ /pubmed/30789967 http://dx.doi.org/10.1371/journal.ppat.1007607 Text en © 2019 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Ping
Liu, Chao
Deng, Wen-Hao
Yao, Dan-Mei
Pan, Li-Long
Li, Yun-Qin
Liu, Yin-Quan
Liang, Yan
Zhou, Xue-Ping
Wang, Xiao-Wei
Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title_full Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title_fullStr Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title_full_unstemmed Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title_short Plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
title_sort plant begomoviruses subvert ubiquitination to suppress plant defenses against insect vectors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400417/
https://www.ncbi.nlm.nih.gov/pubmed/30789967
http://dx.doi.org/10.1371/journal.ppat.1007607
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