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A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem
Numerous insects transmit viruses together with saliva to plant phloem, but the roles of saliva components remain elusive. Here, we report that calcium-binding protein (CBP), a universal insect saliva protein, is modified to benefit horizontal transmission of a devastating rice reovirus into plant p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897447/ https://www.ncbi.nlm.nih.gov/pubmed/35246603 http://dx.doi.org/10.1038/s42003-022-03160-y |
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author | Wu, Wei Yi, Ge Lv, Xinwei Mao, Qianzhuo Wei, Taiyun |
author_facet | Wu, Wei Yi, Ge Lv, Xinwei Mao, Qianzhuo Wei, Taiyun |
author_sort | Wu, Wei |
collection | PubMed |
description | Numerous insects transmit viruses together with saliva to plant phloem, but the roles of saliva components remain elusive. Here, we report that calcium-binding protein (CBP), a universal insect saliva protein, is modified to benefit horizontal transmission of a devastating rice reovirus into plant phloem. CBP effectively competes with virus-induced filaments to target and traverse actin-based apical plasmalemma into saliva-stored cavities in salivary glands of leafhopper vector. Thus, the inhibition of CBP expression by viral infection facilitates filament-mediated viral secretion into salivary cavities and then into plant phloem. Furthermore, virus-mediated reduction of CBP secretion causes an increase of cytosolic Ca(2+) levels in rice, triggering substantial callose deposition and H(2)O(2) production. Thus, viruliferous vectors encounter stronger feeding barriers, probe more frequently, and secrete more saliva into plants, ultimately enhancing viral transmission. We thus conclude that the inhibition of CBP secretion facilitates viral secretion and increases host defense response to benefit viral transmission. |
format | Online Article Text |
id | pubmed-8897447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88974472022-03-08 A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem Wu, Wei Yi, Ge Lv, Xinwei Mao, Qianzhuo Wei, Taiyun Commun Biol Article Numerous insects transmit viruses together with saliva to plant phloem, but the roles of saliva components remain elusive. Here, we report that calcium-binding protein (CBP), a universal insect saliva protein, is modified to benefit horizontal transmission of a devastating rice reovirus into plant phloem. CBP effectively competes with virus-induced filaments to target and traverse actin-based apical plasmalemma into saliva-stored cavities in salivary glands of leafhopper vector. Thus, the inhibition of CBP expression by viral infection facilitates filament-mediated viral secretion into salivary cavities and then into plant phloem. Furthermore, virus-mediated reduction of CBP secretion causes an increase of cytosolic Ca(2+) levels in rice, triggering substantial callose deposition and H(2)O(2) production. Thus, viruliferous vectors encounter stronger feeding barriers, probe more frequently, and secrete more saliva into plants, ultimately enhancing viral transmission. We thus conclude that the inhibition of CBP secretion facilitates viral secretion and increases host defense response to benefit viral transmission. Nature Publishing Group UK 2022-03-04 /pmc/articles/PMC8897447/ /pubmed/35246603 http://dx.doi.org/10.1038/s42003-022-03160-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Wei Yi, Ge Lv, Xinwei Mao, Qianzhuo Wei, Taiyun A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title | A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title_full | A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title_fullStr | A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title_full_unstemmed | A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title_short | A leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
title_sort | leafhopper saliva protein mediates horizontal transmission of viral pathogens from insect vectors into rice phloem |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897447/ https://www.ncbi.nlm.nih.gov/pubmed/35246603 http://dx.doi.org/10.1038/s42003-022-03160-y |
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