Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jia, Dongsheng, Liang, Qifu, Liu, Huan, Li, Guangjun, Zhang, Xiaofeng, Chen, Qian, Wang, Aiming, Wei, Taiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
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
_version_ 1784710701116293120
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
work_keys_str_mv AT jiadongsheng anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liangqifu anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liuhuan anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liguangjun anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT zhangxiaofeng anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT chenqian anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT wangaiming anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT weitaiyun anonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT jiadongsheng nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liangqifu nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liuhuan nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT liguangjun nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT zhangxiaofeng nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT chenqian nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT wangaiming nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors
AT weitaiyun nonstructuralproteinencodedbyaricereovirusinducesanincompleteautophagytopromoteviralspreadininsectvectors