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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...

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Autores principales: Chen, Qian, Zhang, Linghua, Zhang, Yanshuang, Mao, Qianzhuo, Wei, Taiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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