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Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection
Baculoviruses are virulent pathogens that infect a wide range of insects. They initiate infections via specific interactions between the structural proteins on the envelopes of occlusion-derived virions (ODVs) and the midgut cell surface receptors in hosts. However, host factors that are hijacked by...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668127/ https://www.ncbi.nlm.nih.gov/pubmed/36383572 http://dx.doi.org/10.1371/journal.ppat.1010938 |
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author | Liang, Yanting Xu, Weifan Zhou, Yanyan Gao, Yun Tian, Huan Wu, Xiaofeng Xu, Yusong Wang, Huabing |
author_facet | Liang, Yanting Xu, Weifan Zhou, Yanyan Gao, Yun Tian, Huan Wu, Xiaofeng Xu, Yusong Wang, Huabing |
author_sort | Liang, Yanting |
collection | PubMed |
description | Baculoviruses are virulent pathogens that infect a wide range of insects. They initiate infections via specific interactions between the structural proteins on the envelopes of occlusion-derived virions (ODVs) and the midgut cell surface receptors in hosts. However, host factors that are hijacked by baculoviruses for efficient infection remain largely unknown. In this study, we identified a membrane-associated protein sucrose hydrolase (BmSUH) as an ODV binding factor during Bombyx mori nucleopolyhedrovirus (BmNPV) primary infection. BmSUH was specifically expressed in the midgut microvilli where the ODV-midgut fusion happened. Knockout of BmSUH by CRISPR/Cas9 resulted in a significantly higher survival rate after BmNPV orally infection. Liquid chromatography-tandem mass spectrometry analysis and co-immunoprecipitation analysis demonstrated that PIF protein complex required for ODV binding could interact with BmSUH. Furthermore, fluorescence dequenching assay showed that the amount of ODV binding and fusion to the midgut decreased in BmSUH mutants compared to wild-type silkworm, suggesting the role of BmSUH as an ODV binding factor that mediates the ODV entry process. Based on a multilevel survey, the data showed that BmSUH acted as a host factor that facilitates BmNPV oral infection. More generally, this study indicated that disrupting essential protein-protein interactions required for baculovirus efficient entry may be broadly applicable to against viral infection. |
format | Online Article Text |
id | pubmed-9668127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96681272022-11-17 Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection Liang, Yanting Xu, Weifan Zhou, Yanyan Gao, Yun Tian, Huan Wu, Xiaofeng Xu, Yusong Wang, Huabing PLoS Pathog Research Article Baculoviruses are virulent pathogens that infect a wide range of insects. They initiate infections via specific interactions between the structural proteins on the envelopes of occlusion-derived virions (ODVs) and the midgut cell surface receptors in hosts. However, host factors that are hijacked by baculoviruses for efficient infection remain largely unknown. In this study, we identified a membrane-associated protein sucrose hydrolase (BmSUH) as an ODV binding factor during Bombyx mori nucleopolyhedrovirus (BmNPV) primary infection. BmSUH was specifically expressed in the midgut microvilli where the ODV-midgut fusion happened. Knockout of BmSUH by CRISPR/Cas9 resulted in a significantly higher survival rate after BmNPV orally infection. Liquid chromatography-tandem mass spectrometry analysis and co-immunoprecipitation analysis demonstrated that PIF protein complex required for ODV binding could interact with BmSUH. Furthermore, fluorescence dequenching assay showed that the amount of ODV binding and fusion to the midgut decreased in BmSUH mutants compared to wild-type silkworm, suggesting the role of BmSUH as an ODV binding factor that mediates the ODV entry process. Based on a multilevel survey, the data showed that BmSUH acted as a host factor that facilitates BmNPV oral infection. More generally, this study indicated that disrupting essential protein-protein interactions required for baculovirus efficient entry may be broadly applicable to against viral infection. Public Library of Science 2022-11-16 /pmc/articles/PMC9668127/ /pubmed/36383572 http://dx.doi.org/10.1371/journal.ppat.1010938 Text en © 2022 Liang 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 Liang, Yanting Xu, Weifan Zhou, Yanyan Gao, Yun Tian, Huan Wu, Xiaofeng Xu, Yusong Wang, Huabing Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title | Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title_full | Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title_fullStr | Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title_full_unstemmed | Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title_short | Midgut membrane protein BmSUH facilitates Bombyx mori nucleopolyhedrovirus oral infection |
title_sort | midgut membrane protein bmsuh facilitates bombyx mori nucleopolyhedrovirus oral infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668127/ https://www.ncbi.nlm.nih.gov/pubmed/36383572 http://dx.doi.org/10.1371/journal.ppat.1010938 |
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