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A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors
Viruses can hijack autophagosomes as the nonlytic release vehicles in cultured host cells. However, how autophagosome-mediated viral spread occurs in infected host tissues or organs in vivo remains poorly understood. Here, we report that an important rice reovirus, rice gall dwarf virus (RGDV) hijac...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119444/ https://www.ncbi.nlm.nih.gov/pubmed/35533206 http://dx.doi.org/10.1371/journal.ppat.1010506 |
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author | Jia, Dongsheng Liang, Qifu Liu, Huan Li, Guangjun Zhang, Xiaofeng Chen, Qian Wang, Aiming Wei, Taiyun |
author_facet | Jia, Dongsheng Liang, Qifu Liu, Huan Li, Guangjun Zhang, Xiaofeng Chen, Qian Wang, Aiming Wei, Taiyun |
author_sort | Jia, Dongsheng |
collection | PubMed |
description | Viruses can hijack autophagosomes as the nonlytic release vehicles in cultured host cells. However, how autophagosome-mediated viral spread occurs in infected host tissues or organs in vivo remains poorly understood. Here, we report that an important rice reovirus, rice gall dwarf virus (RGDV) hijacks autophagosomes to traverse multiple insect membrane barriers in the midgut and salivary gland of leafhopper vector to enhance viral spread. Such virus-containing double-membraned autophagosomes are prevented from degradation, resulting in increased viral propagation. Mechanistically, viral nonstructural protein Pns11 induces autophagy and embeds itself in the autophagosome membranes. The autophagy-related protein 5 (ATG5)-ATG12 conjugation is essential for initial autophagosome membrane biogenesis. RGDV Pns11 specifically interacts with ATG5, both in vitro and in vivo. Silencing of ATG5 or Pns11 expression suppresses ATG8 lipidation, autophagosome formation, and efficient viral propagation. Thus, Pns11 could directly recruit ATG5-ATG12 conjugation to induce the formation of autophagosomes, facilitating viral spread within the insect bodies. Furthermore, Pns11 potentially blocks autophagosome degradation by directly targeting and mediating the reduced expression of N-glycosylated Lamp1 on lysosomal membranes. Taken together, these results highlight how RGDV remodels autophagosomes to benefit viral propagation in its insect vector. |
format | Online Article Text |
id | pubmed-9119444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-91194442022-05-20 A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors Jia, Dongsheng Liang, Qifu Liu, Huan Li, Guangjun Zhang, Xiaofeng Chen, Qian Wang, Aiming Wei, Taiyun PLoS Pathog Research Article Viruses can hijack autophagosomes as the nonlytic release vehicles in cultured host cells. However, how autophagosome-mediated viral spread occurs in infected host tissues or organs in vivo remains poorly understood. Here, we report that an important rice reovirus, rice gall dwarf virus (RGDV) hijacks autophagosomes to traverse multiple insect membrane barriers in the midgut and salivary gland of leafhopper vector to enhance viral spread. Such virus-containing double-membraned autophagosomes are prevented from degradation, resulting in increased viral propagation. Mechanistically, viral nonstructural protein Pns11 induces autophagy and embeds itself in the autophagosome membranes. The autophagy-related protein 5 (ATG5)-ATG12 conjugation is essential for initial autophagosome membrane biogenesis. RGDV Pns11 specifically interacts with ATG5, both in vitro and in vivo. Silencing of ATG5 or Pns11 expression suppresses ATG8 lipidation, autophagosome formation, and efficient viral propagation. Thus, Pns11 could directly recruit ATG5-ATG12 conjugation to induce the formation of autophagosomes, facilitating viral spread within the insect bodies. Furthermore, Pns11 potentially blocks autophagosome degradation by directly targeting and mediating the reduced expression of N-glycosylated Lamp1 on lysosomal membranes. Taken together, these results highlight how RGDV remodels autophagosomes to benefit viral propagation in its insect vector. Public Library of Science 2022-05-09 /pmc/articles/PMC9119444/ /pubmed/35533206 http://dx.doi.org/10.1371/journal.ppat.1010506 Text en © 2022 Jia et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Jia, Dongsheng Liang, Qifu Liu, Huan Li, Guangjun Zhang, Xiaofeng Chen, Qian Wang, Aiming Wei, Taiyun A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title | A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title_full | A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title_fullStr | A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title_full_unstemmed | A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title_short | A nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
title_sort | nonstructural protein encoded by a rice reovirus induces an incomplete autophagy to promote viral spread in insect vectors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119444/ https://www.ncbi.nlm.nih.gov/pubmed/35533206 http://dx.doi.org/10.1371/journal.ppat.1010506 |
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