Cargando…

Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice

Vesicular trafficking is an important dynamic process that facilitates intracellular transport of biological macromolecules and their release into the extracellular environment. However, little is known about whether or how plant viruses utilize intracellular vesicles to their advantage. Here, we re...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lu, Liu, Wenwen, Zhang, Xiaowan, Li, Li, Wang, Xifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435234/
https://www.ncbi.nlm.nih.gov/pubmed/34390118
http://dx.doi.org/10.1111/mpp.13109
_version_ 1783751751363461120
author Zhang, Lu
Liu, Wenwen
Zhang, Xiaowan
Li, Li
Wang, Xifeng
author_facet Zhang, Lu
Liu, Wenwen
Zhang, Xiaowan
Li, Li
Wang, Xifeng
author_sort Zhang, Lu
collection PubMed
description Vesicular trafficking is an important dynamic process that facilitates intracellular transport of biological macromolecules and their release into the extracellular environment. However, little is known about whether or how plant viruses utilize intracellular vesicles to their advantage. Here, we report that southern rice black‐streaked dwarf virus (SRBSDV) enters intracellular vesicles in epithelial cells of its insect vector by engaging VAMP7 and Vti1a proteins in the soluble N‐ethylmaleimide‐sensitive factor attachment protein receptor (SNARE) complex. The major outer capsid protein P10 of SRBSDV was shown to interact with VAMP7 and Vti1a of the white‐backed planthopper and promote the fusion of vesicles into a large vesicle, which finally fused with the plasma membrane to release virions from midgut epithelial cells. Downregulation of the expression of either VAMP7 or Vti1a did not affect viral entry and accumulation in the gut, but significantly reduced viral accumulation in the haemolymph. It also did not affect virus acquisition, but significantly reduced the virus transmission efficiency to rice. Our data reveal a critical mechanism by which a plant reovirus hijacks the vesicle transport system to overcome the midgut escape barrier in vector insects and provide new insights into the role of the SNARE complex in viral transmission and the potential for developing novel strategies of viral disease control.
format Online
Article
Text
id pubmed-8435234
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84352342021-09-15 Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice Zhang, Lu Liu, Wenwen Zhang, Xiaowan Li, Li Wang, Xifeng Mol Plant Pathol Original Articles Vesicular trafficking is an important dynamic process that facilitates intracellular transport of biological macromolecules and their release into the extracellular environment. However, little is known about whether or how plant viruses utilize intracellular vesicles to their advantage. Here, we report that southern rice black‐streaked dwarf virus (SRBSDV) enters intracellular vesicles in epithelial cells of its insect vector by engaging VAMP7 and Vti1a proteins in the soluble N‐ethylmaleimide‐sensitive factor attachment protein receptor (SNARE) complex. The major outer capsid protein P10 of SRBSDV was shown to interact with VAMP7 and Vti1a of the white‐backed planthopper and promote the fusion of vesicles into a large vesicle, which finally fused with the plasma membrane to release virions from midgut epithelial cells. Downregulation of the expression of either VAMP7 or Vti1a did not affect viral entry and accumulation in the gut, but significantly reduced viral accumulation in the haemolymph. It also did not affect virus acquisition, but significantly reduced the virus transmission efficiency to rice. Our data reveal a critical mechanism by which a plant reovirus hijacks the vesicle transport system to overcome the midgut escape barrier in vector insects and provide new insights into the role of the SNARE complex in viral transmission and the potential for developing novel strategies of viral disease control. John Wiley and Sons Inc. 2021-08-13 /pmc/articles/PMC8435234/ /pubmed/34390118 http://dx.doi.org/10.1111/mpp.13109 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zhang, Lu
Liu, Wenwen
Zhang, Xiaowan
Li, Li
Wang, Xifeng
Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title_full Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title_fullStr Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title_full_unstemmed Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title_short Southern rice black‐streaked dwarf virus hijacks SNARE complex of its insect vector for its effective transmission to rice
title_sort southern rice black‐streaked dwarf virus hijacks snare complex of its insect vector for its effective transmission to rice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435234/
https://www.ncbi.nlm.nih.gov/pubmed/34390118
http://dx.doi.org/10.1111/mpp.13109
work_keys_str_mv AT zhanglu southernriceblackstreakeddwarfvirushijackssnarecomplexofitsinsectvectorforitseffectivetransmissiontorice
AT liuwenwen southernriceblackstreakeddwarfvirushijackssnarecomplexofitsinsectvectorforitseffectivetransmissiontorice
AT zhangxiaowan southernriceblackstreakeddwarfvirushijackssnarecomplexofitsinsectvectorforitseffectivetransmissiontorice
AT lili southernriceblackstreakeddwarfvirushijackssnarecomplexofitsinsectvectorforitseffectivetransmissiontorice
AT wangxifeng southernriceblackstreakeddwarfvirushijackssnarecomplexofitsinsectvectorforitseffectivetransmissiontorice