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Hepatitis B virus hijacks TSG101 to facilitate egress via multiple vesicle bodies
Hepatitis B virus (HBV) chronically infects 296 million individuals and there is no cure. As an important step of viral life cycle, the mechanisms of HBV egress remain poorly elucidated. With proteomic approach to identify capsid protein (HBc) associated host factors and siRNA screen, we uncovered t...
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Published in: | PLoS pathogens 2023-05, Vol.19 (5), p.e1011382-e1011382 |
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creator | Zheng, Yingcheng Wang, Mengfei Li, Sitong Bu, Yanan Xu, Zaichao Zhu, Guoguo Wu, Chuanjian Zhao, Kaitao Li, Aixin Chen, Quan Wang, Jingjing Hua, Rong Teng, Yan Zhao, Li Cheng, Xiaoming Xia, Yuchen |
description | Hepatitis B virus (HBV) chronically infects 296 million individuals and there is no cure. As an important step of viral life cycle, the mechanisms of HBV egress remain poorly elucidated. With proteomic approach to identify capsid protein (HBc) associated host factors and siRNA screen, we uncovered tumor susceptibility gene 101 (TSG101). Knockdown of TSG101 in HBV-producing cells, HBV-infected cells and HBV transgenic mice suppressed HBV release. Co-immunoprecipitation and site mutagenesis revealed that VFND motif in TSG101 and Lys-96 ubiquitination in HBc were essential for TSG101-HBc interaction. In vitro ubiquitination experiment demonstrated that UbcH6 and NEDD4 were potential E2 ubiquitin-conjugating enzyme and E3 ligase that catalyzed HBc ubiquitination, respectively. PPAY motif in HBc and Cys-867 in NEDD4 were required for HBc ubiquitination, TSG101-HBc interaction and HBV egress. Transmission electron microscopy confirmed that TSG101 or NEDD4 knockdown reduces HBV particles count in multivesicular bodies (MVBs). Our work indicates that TSG101 recognition for NEDD4 ubiquitylated HBc is critical for MVBs mediated HBV egress. |
doi_str_mv | 10.1371/journal.ppat.1011382 |
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As an important step of viral life cycle, the mechanisms of HBV egress remain poorly elucidated. With proteomic approach to identify capsid protein (HBc) associated host factors and siRNA screen, we uncovered tumor susceptibility gene 101 (TSG101). Knockdown of TSG101 in HBV-producing cells, HBV-infected cells and HBV transgenic mice suppressed HBV release. Co-immunoprecipitation and site mutagenesis revealed that VFND motif in TSG101 and Lys-96 ubiquitination in HBc were essential for TSG101-HBc interaction. In vitro ubiquitination experiment demonstrated that UbcH6 and NEDD4 were potential E2 ubiquitin-conjugating enzyme and E3 ligase that catalyzed HBc ubiquitination, respectively. PPAY motif in HBc and Cys-867 in NEDD4 were required for HBc ubiquitination, TSG101-HBc interaction and HBV egress. Transmission electron microscopy confirmed that TSG101 or NEDD4 knockdown reduces HBV particles count in multivesicular bodies (MVBs). Our work indicates that TSG101 recognition for NEDD4 ubiquitylated HBc is critical for MVBs mediated HBV egress.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1011382</identifier><identifier>PMID: 37224147</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Antibodies ; Antigens ; Autophagy ; Biology and Life Sciences ; Capsid protein ; Cell culture ; Complications and side effects ; Development and progression ; DNA-Binding Proteins - genetics ; Egress ; Genetic aspects ; Genetic screening ; Genomes ; Heparan sulfate ; Hepatitis ; Hepatitis B ; Hepatitis B virus ; Hepatitis B virus - genetics ; Host-virus relationships ; Immunoprecipitation ; Infections ; Life cycles ; Mass spectrometry ; Medicine and health sciences ; Mice ; Mice, Transgenic ; Mutagenesis ; Physiological aspects ; Proteins ; Proteomics ; Research and Analysis Methods ; Scientific imaging ; siRNA ; Transcription Factors - genetics ; Transgenic animals ; Transgenic mice ; Transmission electron microscopy ; Ubiquitin ; Ubiquitin-conjugating enzyme ; Ubiquitin-protein ligase ; Ubiquitination ; Viral proteins ; Viruses</subject><ispartof>PLoS pathogens, 2023-05, Vol.19 (5), p.e1011382-e1011382</ispartof><rights>Copyright: © 2023 Zheng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Zheng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Zheng et al 2023 Zheng et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c662t-a4825b9e01ee499a5d410b07e808372a3282c7a5362589fde026ab023b3bac283</citedby><cites>FETCH-LOGICAL-c662t-a4825b9e01ee499a5d410b07e808372a3282c7a5362589fde026ab023b3bac283</cites><orcidid>0000-0001-8460-3893</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2826806113/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2826806113?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37224147$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Meyers, Craig</contributor><creatorcontrib>Zheng, Yingcheng</creatorcontrib><creatorcontrib>Wang, Mengfei</creatorcontrib><creatorcontrib>Li, Sitong</creatorcontrib><creatorcontrib>Bu, Yanan</creatorcontrib><creatorcontrib>Xu, Zaichao</creatorcontrib><creatorcontrib>Zhu, Guoguo</creatorcontrib><creatorcontrib>Wu, Chuanjian</creatorcontrib><creatorcontrib>Zhao, Kaitao</creatorcontrib><creatorcontrib>Li, Aixin</creatorcontrib><creatorcontrib>Chen, Quan</creatorcontrib><creatorcontrib>Wang, Jingjing</creatorcontrib><creatorcontrib>Hua, Rong</creatorcontrib><creatorcontrib>Teng, Yan</creatorcontrib><creatorcontrib>Zhao, Li</creatorcontrib><creatorcontrib>Cheng, Xiaoming</creatorcontrib><creatorcontrib>Xia, Yuchen</creatorcontrib><title>Hepatitis B virus hijacks TSG101 to facilitate egress via multiple vesicle bodies</title><title>PLoS pathogens</title><addtitle>PLoS Pathog</addtitle><description>Hepatitis B virus (HBV) chronically infects 296 million individuals and there is no cure. As an important step of viral life cycle, the mechanisms of HBV egress remain poorly elucidated. With proteomic approach to identify capsid protein (HBc) associated host factors and siRNA screen, we uncovered tumor susceptibility gene 101 (TSG101). Knockdown of TSG101 in HBV-producing cells, HBV-infected cells and HBV transgenic mice suppressed HBV release. Co-immunoprecipitation and site mutagenesis revealed that VFND motif in TSG101 and Lys-96 ubiquitination in HBc were essential for TSG101-HBc interaction. In vitro ubiquitination experiment demonstrated that UbcH6 and NEDD4 were potential E2 ubiquitin-conjugating enzyme and E3 ligase that catalyzed HBc ubiquitination, respectively. PPAY motif in HBc and Cys-867 in NEDD4 were required for HBc ubiquitination, TSG101-HBc interaction and HBV egress. Transmission electron microscopy confirmed that TSG101 or NEDD4 knockdown reduces HBV particles count in multivesicular bodies (MVBs). Our work indicates that TSG101 recognition for NEDD4 ubiquitylated HBc is critical for MVBs mediated HBV egress.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Autophagy</subject><subject>Biology and Life Sciences</subject><subject>Capsid protein</subject><subject>Cell culture</subject><subject>Complications and side effects</subject><subject>Development and progression</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Egress</subject><subject>Genetic aspects</subject><subject>Genetic screening</subject><subject>Genomes</subject><subject>Heparan sulfate</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - genetics</subject><subject>Host-virus relationships</subject><subject>Immunoprecipitation</subject><subject>Infections</subject><subject>Life cycles</subject><subject>Mass spectrometry</subject><subject>Medicine and health sciences</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mutagenesis</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Proteomics</subject><subject>Research and Analysis Methods</subject><subject>Scientific imaging</subject><subject>siRNA</subject><subject>Transcription Factors - genetics</subject><subject>Transgenic animals</subject><subject>Transgenic mice</subject><subject>Transmission electron microscopy</subject><subject>Ubiquitin</subject><subject>Ubiquitin-conjugating enzyme</subject><subject>Ubiquitin-protein ligase</subject><subject>Ubiquitination</subject><subject>Viral proteins</subject><subject>Viruses</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqVkktv1DAUhSMEog_4BwgisYHFDH7FdlZVqaAdqQJBy9pynJvUQyYOtjMq_x6HSasO6gZl4cj-zrn3Ht0se4XRElOBP6zd6HvdLYdBxyVGGFNJnmSHuCjoQlDBnj74P8iOQlgjxDDF_Hl2QAUhDDNxmH27gKS30Yb8Y761fgz5jV1r8zPk11fnyTaPLm-0sZ2NOkIOrYcQEqnzzdhFO3SQbyFYk87K1RbCi-xZo7sAL-fzOPvx-dP12cXi8uv56uz0cmE4J3GhmSRFVQLCAKwsdVEzjCokQCKZ2tOUSGKELignhSybGhDhukKEVrTShkh6nL3Z-Q6dC2pOI6gk4xLxFEciVjuidnqtBm832v9WTlv198L5Vmkfp9YVwSUmtUh9VCXjmFU1R6IpCBhTC8knr5O52lhtoDbQR6-7PdP9l97eqNZtFUYESSaL5PBudvDu1wghqo0NBrpO9-DGqXFcEiFpOY329h_08fFmqtVpAts3LhU2k6k6FQXmKCU5lV0-QqWvho01rofGpvs9wfs9QWIi3MZWjyGo1dX3_2C_7LNsxxrvQvDQ3IeHkZo2-m5INW20mjc6yV4_DP5edLfC9A9MfO6_</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Zheng, Yingcheng</creator><creator>Wang, Mengfei</creator><creator>Li, Sitong</creator><creator>Bu, Yanan</creator><creator>Xu, Zaichao</creator><creator>Zhu, Guoguo</creator><creator>Wu, Chuanjian</creator><creator>Zhao, Kaitao</creator><creator>Li, Aixin</creator><creator>Chen, Quan</creator><creator>Wang, Jingjing</creator><creator>Hua, Rong</creator><creator>Teng, Yan</creator><creator>Zhao, Li</creator><creator>Cheng, Xiaoming</creator><creator>Xia, Yuchen</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8460-3893</orcidid></search><sort><creationdate>20230501</creationdate><title>Hepatitis B virus hijacks TSG101 to facilitate egress via multiple vesicle bodies</title><author>Zheng, Yingcheng ; Wang, Mengfei ; Li, Sitong ; Bu, Yanan ; Xu, Zaichao ; Zhu, Guoguo ; Wu, Chuanjian ; Zhao, Kaitao ; Li, Aixin ; Chen, Quan ; Wang, Jingjing ; Hua, Rong ; Teng, Yan ; Zhao, Li ; Cheng, Xiaoming ; Xia, Yuchen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c662t-a4825b9e01ee499a5d410b07e808372a3282c7a5362589fde026ab023b3bac283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>Autophagy</topic><topic>Biology and Life Sciences</topic><topic>Capsid protein</topic><topic>Cell culture</topic><topic>Complications and side effects</topic><topic>Development and progression</topic><topic>DNA-Binding Proteins - 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As an important step of viral life cycle, the mechanisms of HBV egress remain poorly elucidated. With proteomic approach to identify capsid protein (HBc) associated host factors and siRNA screen, we uncovered tumor susceptibility gene 101 (TSG101). Knockdown of TSG101 in HBV-producing cells, HBV-infected cells and HBV transgenic mice suppressed HBV release. Co-immunoprecipitation and site mutagenesis revealed that VFND motif in TSG101 and Lys-96 ubiquitination in HBc were essential for TSG101-HBc interaction. In vitro ubiquitination experiment demonstrated that UbcH6 and NEDD4 were potential E2 ubiquitin-conjugating enzyme and E3 ligase that catalyzed HBc ubiquitination, respectively. PPAY motif in HBc and Cys-867 in NEDD4 were required for HBc ubiquitination, TSG101-HBc interaction and HBV egress. Transmission electron microscopy confirmed that TSG101 or NEDD4 knockdown reduces HBV particles count in multivesicular bodies (MVBs). 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subjects | Animals Antibodies Antigens Autophagy Biology and Life Sciences Capsid protein Cell culture Complications and side effects Development and progression DNA-Binding Proteins - genetics Egress Genetic aspects Genetic screening Genomes Heparan sulfate Hepatitis Hepatitis B Hepatitis B virus Hepatitis B virus - genetics Host-virus relationships Immunoprecipitation Infections Life cycles Mass spectrometry Medicine and health sciences Mice Mice, Transgenic Mutagenesis Physiological aspects Proteins Proteomics Research and Analysis Methods Scientific imaging siRNA Transcription Factors - genetics Transgenic animals Transgenic mice Transmission electron microscopy Ubiquitin Ubiquitin-conjugating enzyme Ubiquitin-protein ligase Ubiquitination Viral proteins Viruses |
title | Hepatitis B virus hijacks TSG101 to facilitate egress via multiple vesicle bodies |
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