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Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector
Plant reoviruses are known to exploit virion-packaging tubules formed by virus-encoding non-structural proteins for viral spread in insect vectors. Tubules are propelled by actin-based tubule motility (ABTM) to overcome membrane or tissue barriers in insect vectors. To further understand which insec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220352/ https://www.ncbi.nlm.nih.gov/pubmed/28067229 http://dx.doi.org/10.1038/srep38563 |
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author | Chen, Qian Zhang, Linghua Zhang, Yanshuang Mao, Qianzhuo Wei, Taiyun |
author_facet | Chen, Qian Zhang, Linghua Zhang, Yanshuang Mao, Qianzhuo Wei, Taiyun |
author_sort | Chen, Qian |
collection | PubMed |
description | Plant reoviruses are known to exploit virion-packaging tubules formed by virus-encoding non-structural proteins for viral spread in insect vectors. Tubules are propelled by actin-based tubule motility (ABTM) to overcome membrane or tissue barriers in insect vectors. To further understand which insect factors mediate ABTM, we utilized yeast two-hybrid and bimolecular fluorescence complementation assays to test interactions between tubule protein Pns10 of rice dwarf virus (RDV), a plant reovirus, and proteins of its insect vector, the leafhopper Nephotettix cincticeps. Tropomodulin (Tmod), vitellogenin, and lipophorin precursor of N. cincticep displayed positive and strong interaction with Pns10, and actin-associated protein Tmod interacted with Pns10 in pull-down assay and the co-immunoprecipitation system. Further, we determined Pns10 tubules associated with Tmod in cultured cells and midgut of N. cincticep. The expression dynamic of Tmod was consistent with that of Pns10 and the fluctuation of RDV accumulation. Knockdown of Tmod inhibited the Pns10 expression and viral accumulation, thus decreasing the viruliferous rates of leafhopper. These results suggested that Tmod was involved in viral spread by directly interacting with Pns10 tubules, finally promoting RDV infection. This study provided direct evidence of plant reoviruses utilizing an actin-associated protein to manipulate ABTM in insect vectors, thus facilitating viral spread. |
format | Online Article Text |
id | pubmed-5220352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52203522017-01-11 Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector Chen, Qian Zhang, Linghua Zhang, Yanshuang Mao, Qianzhuo Wei, Taiyun Sci Rep Article Plant reoviruses are known to exploit virion-packaging tubules formed by virus-encoding non-structural proteins for viral spread in insect vectors. Tubules are propelled by actin-based tubule motility (ABTM) to overcome membrane or tissue barriers in insect vectors. To further understand which insect factors mediate ABTM, we utilized yeast two-hybrid and bimolecular fluorescence complementation assays to test interactions between tubule protein Pns10 of rice dwarf virus (RDV), a plant reovirus, and proteins of its insect vector, the leafhopper Nephotettix cincticeps. Tropomodulin (Tmod), vitellogenin, and lipophorin precursor of N. cincticep displayed positive and strong interaction with Pns10, and actin-associated protein Tmod interacted with Pns10 in pull-down assay and the co-immunoprecipitation system. Further, we determined Pns10 tubules associated with Tmod in cultured cells and midgut of N. cincticep. The expression dynamic of Tmod was consistent with that of Pns10 and the fluctuation of RDV accumulation. Knockdown of Tmod inhibited the Pns10 expression and viral accumulation, thus decreasing the viruliferous rates of leafhopper. These results suggested that Tmod was involved in viral spread by directly interacting with Pns10 tubules, finally promoting RDV infection. This study provided direct evidence of plant reoviruses utilizing an actin-associated protein to manipulate ABTM in insect vectors, thus facilitating viral spread. Nature Publishing Group 2017-01-09 /pmc/articles/PMC5220352/ /pubmed/28067229 http://dx.doi.org/10.1038/srep38563 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Qian Zhang, Linghua Zhang, Yanshuang Mao, Qianzhuo Wei, Taiyun Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title | Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title_full | Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title_fullStr | Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title_full_unstemmed | Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title_short | Tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
title_sort | tubules of plant reoviruses exploit tropomodulin to regulate actin-based tubule motility in insect vector |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220352/ https://www.ncbi.nlm.nih.gov/pubmed/28067229 http://dx.doi.org/10.1038/srep38563 |
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