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Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors
Maintenance of a balance between the levels of viral replication and selective pressure from the immune systems of insect vectors is one of the prerequisites for efficient transmission of insect-borne propagative phytoviruses. The mechanism regulating the adaptation of RNA viruses to insect vectors...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984632/ https://www.ncbi.nlm.nih.gov/pubmed/33690727 http://dx.doi.org/10.1371/journal.ppat.1009424 |
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author | Zhao, Wan Yu, Jinting Jiang, Feng Wang, Wei Kang, Le Cui, Feng |
author_facet | Zhao, Wan Yu, Jinting Jiang, Feng Wang, Wei Kang, Le Cui, Feng |
author_sort | Zhao, Wan |
collection | PubMed |
description | Maintenance of a balance between the levels of viral replication and selective pressure from the immune systems of insect vectors is one of the prerequisites for efficient transmission of insect-borne propagative phytoviruses. The mechanism regulating the adaptation of RNA viruses to insect vectors by genomic variation remains unknown. Our previous study demonstrated an extension of the 3’-untranslated terminal region (UTR) of two genomic segments of rice stripe virus (RSV). In the present study, a reverse genetic system for RSV in human cells and an insect vector, the small brown planthopper Laodelphax striatellus, was used to demonstrate that the 3’-terminal extensions suppressed viral replication in vector insects by inhibiting promoter activity due to structural interference with the panhandle structure formed by viral 3’- and 5’-UTRs. The extension sequence in the viral RNA1 segment was targeted by an endogenous insect microRNA, miR-263a, which decreased the inhibitory effect of the extension sequence on viral promoter activity. Surprisingly, the expression of miR-263a was negatively regulated by RSV infection. This elaborate coordination between terminal variation of the viral genome and endogenous insect microRNAs controls RSV replication in planthopper, thus reflecting a distinct strategy of adaptation of phytoviruses to insect vectors. |
format | Online Article Text |
id | pubmed-7984632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-79846322021-04-01 Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors Zhao, Wan Yu, Jinting Jiang, Feng Wang, Wei Kang, Le Cui, Feng PLoS Pathog Research Article Maintenance of a balance between the levels of viral replication and selective pressure from the immune systems of insect vectors is one of the prerequisites for efficient transmission of insect-borne propagative phytoviruses. The mechanism regulating the adaptation of RNA viruses to insect vectors by genomic variation remains unknown. Our previous study demonstrated an extension of the 3’-untranslated terminal region (UTR) of two genomic segments of rice stripe virus (RSV). In the present study, a reverse genetic system for RSV in human cells and an insect vector, the small brown planthopper Laodelphax striatellus, was used to demonstrate that the 3’-terminal extensions suppressed viral replication in vector insects by inhibiting promoter activity due to structural interference with the panhandle structure formed by viral 3’- and 5’-UTRs. The extension sequence in the viral RNA1 segment was targeted by an endogenous insect microRNA, miR-263a, which decreased the inhibitory effect of the extension sequence on viral promoter activity. Surprisingly, the expression of miR-263a was negatively regulated by RSV infection. This elaborate coordination between terminal variation of the viral genome and endogenous insect microRNAs controls RSV replication in planthopper, thus reflecting a distinct strategy of adaptation of phytoviruses to insect vectors. Public Library of Science 2021-03-10 /pmc/articles/PMC7984632/ /pubmed/33690727 http://dx.doi.org/10.1371/journal.ppat.1009424 Text en © 2021 Zhao 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 Zhao, Wan Yu, Jinting Jiang, Feng Wang, Wei Kang, Le Cui, Feng Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title | Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title_full | Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title_fullStr | Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title_full_unstemmed | Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title_short | Coordination between terminal variation of the viral genome and insect microRNAs regulates rice stripe virus replication in insect vectors |
title_sort | coordination between terminal variation of the viral genome and insect micrornas regulates rice stripe virus replication in insect vectors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984632/ https://www.ncbi.nlm.nih.gov/pubmed/33690727 http://dx.doi.org/10.1371/journal.ppat.1009424 |
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