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Presence of Intact Hepatitis B Virions in Exosomes
Hepatitis B virus (HBV) was identified as an enveloped DNA virus with a diameter of 42 nm. Multivesicular bodies play a central role in HBV egress and exosome biogenesis. In light of this, it was studied whether intact virions wrapped in exosomes are released by HBV-producing cells. Robust methods f...
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Published in: | Cellular and molecular gastroenterology and hepatology 2023-01, Vol.15 (1), p.237-259 |
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creator | Wu, Qingyan Glitscher, Mirco Tonnemacher, Susanne Schollmeier, Anja Raupach, Jan Zahn, Tobias Eberle, Regina Krijnse-Locker, Jacomine Basic, Michael Hildt, Eberhard |
description | Hepatitis B virus (HBV) was identified as an enveloped DNA virus with a diameter of 42 nm. Multivesicular bodies play a central role in HBV egress and exosome biogenesis. In light of this, it was studied whether intact virions wrapped in exosomes are released by HBV-producing cells.
Robust methods for efficient separation of exosomes from virions were established. Exosomes were subjected to limited detergent treatment for release of viral particles. Electron microscopy of immunogold labeled ultrathin sections of purified exosomes was performed for characterization of exosomal HBV. Exosome formation/release was affected by inhibitors or Crispr/Cas-mediated gene silencing. Infectivity/uptake of exosomal HBV was investigated in susceptible and non-susceptible cells.
Exosomes could be isolated from supernatants of HBV-producing cells, which are characterized by the presence of exosomal and HBV markers. These exosomal fractions could be separated from the fractions containing free virions. Limited detergent treatment of exosomes causes stepwise release of intact HBV virions and naked capsids. Inhibition of exosome morphogenesis impairs the release of exosome-wrapped HBV. Electron microscopy confirmed the presence of intact virions in exosomes. Moreover, the presence of large hepatitis B virus surface antigen on the surface of exosomes derived from HBV expressing cells was observed, which conferred exosome-encapsulated HBV initiating infection in susceptible cells in a , large hepatitis B virus surface antigen/Na+–taurocholate co-transporting polypeptide-dependent manner. The uptake of exosomal HBV with low efficiency was also observed in non-permissive cells.
These data indicate that a fraction of intact HBV virions can be released as exosomes. This reveals a so far not described release pathway for HBV.
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doi_str_mv | 10.1016/j.jcmgh.2022.09.012 |
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Robust methods for efficient separation of exosomes from virions were established. Exosomes were subjected to limited detergent treatment for release of viral particles. Electron microscopy of immunogold labeled ultrathin sections of purified exosomes was performed for characterization of exosomal HBV. Exosome formation/release was affected by inhibitors or Crispr/Cas-mediated gene silencing. Infectivity/uptake of exosomal HBV was investigated in susceptible and non-susceptible cells.
Exosomes could be isolated from supernatants of HBV-producing cells, which are characterized by the presence of exosomal and HBV markers. These exosomal fractions could be separated from the fractions containing free virions. Limited detergent treatment of exosomes causes stepwise release of intact HBV virions and naked capsids. Inhibition of exosome morphogenesis impairs the release of exosome-wrapped HBV. Electron microscopy confirmed the presence of intact virions in exosomes. Moreover, the presence of large hepatitis B virus surface antigen on the surface of exosomes derived from HBV expressing cells was observed, which conferred exosome-encapsulated HBV initiating infection in susceptible cells in a , large hepatitis B virus surface antigen/Na+–taurocholate co-transporting polypeptide-dependent manner. The uptake of exosomal HBV with low efficiency was also observed in non-permissive cells.
These data indicate that a fraction of intact HBV virions can be released as exosomes. This reveals a so far not described release pathway for HBV.
▪</description><identifier>ISSN: 2352-345X</identifier><identifier>EISSN: 2352-345X</identifier><identifier>DOI: 10.1016/j.jcmgh.2022.09.012</identifier><identifier>PMID: 36184032</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antigens, Surface - metabolism ; Detergents - metabolism ; Exosomes ; Hepatitis B - metabolism ; Hepatitis B virus - genetics ; Humans ; MVB ; Original Research ; Ultrathin Cryosection ; Virion ; Virion Egress ; Virus-host Interaction</subject><ispartof>Cellular and molecular gastroenterology and hepatology, 2023-01, Vol.15 (1), p.237-259</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.</rights><rights>2022 The Authors 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-f45f0b0d509cb7e33bd60592a9fadefecc57d9d998161323c8a7f1b56c359cc23</citedby><cites>FETCH-LOGICAL-c459t-f45f0b0d509cb7e33bd60592a9fadefecc57d9d998161323c8a7f1b56c359cc23</cites><orcidid>0000-0002-3020-9564</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676402/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2352345X22002077$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,3536,27905,27906,45761,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36184032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Qingyan</creatorcontrib><creatorcontrib>Glitscher, Mirco</creatorcontrib><creatorcontrib>Tonnemacher, Susanne</creatorcontrib><creatorcontrib>Schollmeier, Anja</creatorcontrib><creatorcontrib>Raupach, Jan</creatorcontrib><creatorcontrib>Zahn, Tobias</creatorcontrib><creatorcontrib>Eberle, Regina</creatorcontrib><creatorcontrib>Krijnse-Locker, Jacomine</creatorcontrib><creatorcontrib>Basic, Michael</creatorcontrib><creatorcontrib>Hildt, Eberhard</creatorcontrib><title>Presence of Intact Hepatitis B Virions in Exosomes</title><title>Cellular and molecular gastroenterology and hepatology</title><addtitle>Cell Mol Gastroenterol Hepatol</addtitle><description>Hepatitis B virus (HBV) was identified as an enveloped DNA virus with a diameter of 42 nm. Multivesicular bodies play a central role in HBV egress and exosome biogenesis. In light of this, it was studied whether intact virions wrapped in exosomes are released by HBV-producing cells.
Robust methods for efficient separation of exosomes from virions were established. Exosomes were subjected to limited detergent treatment for release of viral particles. Electron microscopy of immunogold labeled ultrathin sections of purified exosomes was performed for characterization of exosomal HBV. Exosome formation/release was affected by inhibitors or Crispr/Cas-mediated gene silencing. Infectivity/uptake of exosomal HBV was investigated in susceptible and non-susceptible cells.
Exosomes could be isolated from supernatants of HBV-producing cells, which are characterized by the presence of exosomal and HBV markers. These exosomal fractions could be separated from the fractions containing free virions. Limited detergent treatment of exosomes causes stepwise release of intact HBV virions and naked capsids. Inhibition of exosome morphogenesis impairs the release of exosome-wrapped HBV. Electron microscopy confirmed the presence of intact virions in exosomes. Moreover, the presence of large hepatitis B virus surface antigen on the surface of exosomes derived from HBV expressing cells was observed, which conferred exosome-encapsulated HBV initiating infection in susceptible cells in a , large hepatitis B virus surface antigen/Na+–taurocholate co-transporting polypeptide-dependent manner. The uptake of exosomal HBV with low efficiency was also observed in non-permissive cells.
These data indicate that a fraction of intact HBV virions can be released as exosomes. This reveals a so far not described release pathway for HBV.
▪</description><subject>Antigens, Surface - metabolism</subject><subject>Detergents - metabolism</subject><subject>Exosomes</subject><subject>Hepatitis B - metabolism</subject><subject>Hepatitis B virus - genetics</subject><subject>Humans</subject><subject>MVB</subject><subject>Original Research</subject><subject>Ultrathin Cryosection</subject><subject>Virion</subject><subject>Virion Egress</subject><subject>Virus-host Interaction</subject><issn>2352-345X</issn><issn>2352-345X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kM9LwzAUx4MoKrq_QJAevay-JE27HBR0-GMw0IOKt5Cmr5rSNjPphv73dm6OefH0Hrzvj8eHkBMKMQWanldxZZq395gBYzHIGCjbIYeMCzbkiXjd3doPyCCECgBokqUZiH1ywFM6SoCzQ8IePQZsDUaujCZtp00X3eNMd7azIbqOXqy3rg2RbaObTxdcg-GY7JW6DjhYzyPyfHvzNL4fTh_uJuOr6dAkQnbDMhEl5FAIkCbPkPO8SEFIpmWpCyzRGJEVspByRFPKGTcjnZU0F6nhQhrD-BG5XOXO5nmDhcG287pWM28b7b-U01b9vbT2Xb25hZJpliawDDhbB3j3McfQqcYGg3WtW3TzoFjGQHIQVPRSvpIa70LwWG5qKKglcFWpH-BqCVyBVD3w3nW6_eHG84u3F1ysBNhzWlj0Khi7pF1Yj6ZThbP_FnwDRquSvQ</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Wu, Qingyan</creator><creator>Glitscher, Mirco</creator><creator>Tonnemacher, Susanne</creator><creator>Schollmeier, Anja</creator><creator>Raupach, Jan</creator><creator>Zahn, Tobias</creator><creator>Eberle, Regina</creator><creator>Krijnse-Locker, Jacomine</creator><creator>Basic, Michael</creator><creator>Hildt, Eberhard</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3020-9564</orcidid></search><sort><creationdate>20230101</creationdate><title>Presence of Intact Hepatitis B Virions in Exosomes</title><author>Wu, Qingyan ; Glitscher, Mirco ; Tonnemacher, Susanne ; Schollmeier, Anja ; Raupach, Jan ; Zahn, Tobias ; Eberle, Regina ; Krijnse-Locker, Jacomine ; Basic, Michael ; Hildt, Eberhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-f45f0b0d509cb7e33bd60592a9fadefecc57d9d998161323c8a7f1b56c359cc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antigens, Surface - metabolism</topic><topic>Detergents - metabolism</topic><topic>Exosomes</topic><topic>Hepatitis B - metabolism</topic><topic>Hepatitis B virus - genetics</topic><topic>Humans</topic><topic>MVB</topic><topic>Original Research</topic><topic>Ultrathin Cryosection</topic><topic>Virion</topic><topic>Virion Egress</topic><topic>Virus-host Interaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Qingyan</creatorcontrib><creatorcontrib>Glitscher, Mirco</creatorcontrib><creatorcontrib>Tonnemacher, Susanne</creatorcontrib><creatorcontrib>Schollmeier, Anja</creatorcontrib><creatorcontrib>Raupach, Jan</creatorcontrib><creatorcontrib>Zahn, Tobias</creatorcontrib><creatorcontrib>Eberle, Regina</creatorcontrib><creatorcontrib>Krijnse-Locker, Jacomine</creatorcontrib><creatorcontrib>Basic, Michael</creatorcontrib><creatorcontrib>Hildt, Eberhard</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cellular and molecular gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Qingyan</au><au>Glitscher, Mirco</au><au>Tonnemacher, Susanne</au><au>Schollmeier, Anja</au><au>Raupach, Jan</au><au>Zahn, Tobias</au><au>Eberle, Regina</au><au>Krijnse-Locker, Jacomine</au><au>Basic, Michael</au><au>Hildt, Eberhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presence of Intact Hepatitis B Virions in Exosomes</atitle><jtitle>Cellular and molecular gastroenterology and hepatology</jtitle><addtitle>Cell Mol Gastroenterol Hepatol</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>15</volume><issue>1</issue><spage>237</spage><epage>259</epage><pages>237-259</pages><issn>2352-345X</issn><eissn>2352-345X</eissn><abstract>Hepatitis B virus (HBV) was identified as an enveloped DNA virus with a diameter of 42 nm. Multivesicular bodies play a central role in HBV egress and exosome biogenesis. In light of this, it was studied whether intact virions wrapped in exosomes are released by HBV-producing cells.
Robust methods for efficient separation of exosomes from virions were established. Exosomes were subjected to limited detergent treatment for release of viral particles. Electron microscopy of immunogold labeled ultrathin sections of purified exosomes was performed for characterization of exosomal HBV. Exosome formation/release was affected by inhibitors or Crispr/Cas-mediated gene silencing. Infectivity/uptake of exosomal HBV was investigated in susceptible and non-susceptible cells.
Exosomes could be isolated from supernatants of HBV-producing cells, which are characterized by the presence of exosomal and HBV markers. These exosomal fractions could be separated from the fractions containing free virions. Limited detergent treatment of exosomes causes stepwise release of intact HBV virions and naked capsids. Inhibition of exosome morphogenesis impairs the release of exosome-wrapped HBV. Electron microscopy confirmed the presence of intact virions in exosomes. Moreover, the presence of large hepatitis B virus surface antigen on the surface of exosomes derived from HBV expressing cells was observed, which conferred exosome-encapsulated HBV initiating infection in susceptible cells in a , large hepatitis B virus surface antigen/Na+–taurocholate co-transporting polypeptide-dependent manner. The uptake of exosomal HBV with low efficiency was also observed in non-permissive cells.
These data indicate that a fraction of intact HBV virions can be released as exosomes. This reveals a so far not described release pathway for HBV.
▪</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>36184032</pmid><doi>10.1016/j.jcmgh.2022.09.012</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0002-3020-9564</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, Surface - metabolism Detergents - metabolism Exosomes Hepatitis B - metabolism Hepatitis B virus - genetics Humans MVB Original Research Ultrathin Cryosection Virion Virion Egress Virus-host Interaction |
title | Presence of Intact Hepatitis B Virions in Exosomes |
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