{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhao P"],"funding":["Chinese Academy of Sciences, Strategic Priority Research Program Grant","National Natural Science Foundation of China-Yunnan Joint Fund","National Natural Science Foundation of China","China Postdoctoral Science Foundation"],"pagination":["eaav9801"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6703867"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["5(8)"],"pubmed_abstract":["A parasite-infected host may promote performance of associated insect vectors; but possible parasite effects on nonvector insects have been largely unexplored. Here, we show that <i>Begomovirus</i>, the largest genus of plant viruses and transmitted exclusively by whitefly, reprogram plant immunity to promote the fitness of the vector and suppress performance of nonvector insects (i.e., cotton bollworm and aphid). Infected plants accumulated begomoviral βC1 proteins in the phloem where they were bound to the plant transcription factor WRKY20. This viral hijacking of WRKY20 spatiotemporally redeployed plant chemical immunity within the leaf and had the asymmetrical benefiting effects on the begomoviruses and its whitefly vectors while negatively affecting two nonvector competitors. This typ"],"journal":["Science advances"],"pubmed_title":["Viruses mobilize plant immunity to deter nonvector insect herbivores."],"pmcid":["PMC6703867"],"funding_grant_id":["31830073","XDB11040300","31390421","2016M600142","31701783","31522046","31672001"],"pubmed_authors":["Kliebenstein DJ","Liu SS","Fang RX","Li R","Yao X","Sun Y","Wang M","Zou Z","Cai C","Wang Q","Zhao P","Du J","Ye J"],"additional_accession":[]},"is_claimable":false,"name":"Viruses mobilize plant immunity to deter nonvector insect herbivores.","description":"A parasite-infected host may promote performance of associated insect vectors; but possible parasite effects on nonvector insects have been largely unexplored. Here, we show that <i>Begomovirus</i>, the largest genus of plant viruses and transmitted exclusively by whitefly, reprogram plant immunity to promote the fitness of the vector and suppress performance of nonvector insects (i.e., cotton bollworm and aphid). Infected plants accumulated begomoviral βC1 proteins in the phloem where they were bound to the plant transcription factor WRKY20. This viral hijacking of WRKY20 spatiotemporally redeployed plant chemical immunity within the leaf and had the asymmetrical benefiting effects on the begomoviruses and its whitefly vectors while negatively affecting two nonvector competitors. This typ","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Aug","modification":"2026-05-07T05:31:03.756Z","creation":"2019-08-31T07:06:48Z"},"accession":"S-EPMC6703867","cross_references":{"pubmed":["31457079"],"doi":["10.1126/sciadv.aav9801"]}}