Plasma membrane is the site of productive HIV-1 particle assembly
Recently proposed models that have gained wide acceptance posit that HIV-1 virion morphogenesis is initiated by targeting the major structural protein (Gag) to late endosomal membranes. Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma m...
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description | Recently proposed models that have gained wide acceptance posit that HIV-1 virion morphogenesis is initiated by targeting the major structural protein (Gag) to late endosomal membranes. Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma membrane (PM) and extracellular milieu. We present several findings that are inconsistent with this model. Specifically, we demonstrate that HIV-1 Gag is delivered to the PM, and virions are efficiently released into the extracellular medium, when late endosome motility is abolished. Furthermore, we show that HIV-1 virions are efficiently released when assembly is rationally targeted to the PM, but not when targeted to late endosomes. Recently synthesized Gag first accumulates and assembles at the PM, but a proportion is subsequently internalized via endocytosis or phagocytosis, thus accounting for observations of endosomal localization. We conclude that HIV-1 assembly is initiated and completed at the PM, and not at endosomal membranes. |
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Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma membrane (PM) and extracellular milieu. We present several findings that are inconsistent with this model. Specifically, we demonstrate that HIV-1 Gag is delivered to the PM, and virions are efficiently released into the extracellular medium, when late endosome motility is abolished. Furthermore, we show that HIV-1 virions are efficiently released when assembly is rationally targeted to the PM, but not when targeted to late endosomes. Recently synthesized Gag first accumulates and assembles at the PM, but a proportion is subsequently internalized via endocytosis or phagocytosis, thus accounting for observations of endosomal localization. We conclude that HIV-1 assembly is initiated and completed at the PM, and not at endosomal membranes.</description><identifier>ISSN: 1545-7885</identifier><identifier>ISSN: 1544-9173</identifier><identifier>EISSN: 1545-7885</identifier><identifier>DOI: 10.1371/journal.pbio.0040435</identifier><identifier>PMID: 17147474</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Actins - metabolism ; Biological Transport ; Cell Biology ; Cell Membrane - metabolism ; Cell membranes ; Cells, Cultured ; Cellular biology ; Endocytosis ; Endosomes - metabolism ; Gene Products, gag - genetics ; Gene Products, gag - metabolism ; Gene Products, gag - ultrastructure ; Genetic aspects ; HIV (Viruses) ; HIV-1 - genetics ; HIV-1 - metabolism ; HIV-1 - ultrastructure ; Humans ; Infectious Diseases ; Kinases ; Leukemia ; Macrophages - metabolism ; Membranes ; Microscopy, Electron, Transmission ; Microtubules - metabolism ; Plasma ; Proteins ; Virion - genetics ; Virion - metabolism ; Virion - ultrastructure ; Virology ; Virus Assembly ; Viruses</subject><ispartof>PLoS biology, 2006-12, Vol.4 (12), p.e435-e435</ispartof><rights>COPYRIGHT 2006 Public Library of Science</rights><rights>2006 Jouvenet 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: Jouvenet N, Neil SJD, Bess C, Johnson MC, Virgen CA, et al. (2006) Plasma Membrane Is the Site of Productive HIV-1 Particle Assembly. PLoS Biol 4(12): e435. doi:10.1371/journal.pbio.0040435</rights><rights>2006 Jouvenet et al 2006 Jouvenet et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c829t-d06c29356149fa7c8b685694a4d6b71f834fd73088506f3d772332bc193e49c03</citedby><cites>FETCH-LOGICAL-c829t-d06c29356149fa7c8b685694a4d6b71f834fd73088506f3d772332bc193e49c03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1750931/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1750931/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17147474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jouvenet, Nolwenn</creatorcontrib><creatorcontrib>Neil, Stuart J D</creatorcontrib><creatorcontrib>Bess, Cameron</creatorcontrib><creatorcontrib>Johnson, Marc C</creatorcontrib><creatorcontrib>Virgen, Cesar A</creatorcontrib><creatorcontrib>Simon, Sanford M</creatorcontrib><creatorcontrib>Bieniasz, Paul D</creatorcontrib><title>Plasma membrane is the site of productive HIV-1 particle assembly</title><title>PLoS biology</title><addtitle>PLoS Biol</addtitle><description>Recently proposed models that have gained wide acceptance posit that HIV-1 virion morphogenesis is initiated by targeting the major structural protein (Gag) to late endosomal membranes. Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma membrane (PM) and extracellular milieu. We present several findings that are inconsistent with this model. Specifically, we demonstrate that HIV-1 Gag is delivered to the PM, and virions are efficiently released into the extracellular medium, when late endosome motility is abolished. Furthermore, we show that HIV-1 virions are efficiently released when assembly is rationally targeted to the PM, but not when targeted to late endosomes. Recently synthesized Gag first accumulates and assembles at the PM, but a proportion is subsequently internalized via endocytosis or phagocytosis, thus accounting for observations of endosomal localization. We conclude that HIV-1 assembly is initiated and completed at the PM, and not at endosomal membranes.</description><subject>Actins - metabolism</subject><subject>Biological Transport</subject><subject>Cell Biology</subject><subject>Cell Membrane - metabolism</subject><subject>Cell membranes</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>Endocytosis</subject><subject>Endosomes - metabolism</subject><subject>Gene Products, gag - genetics</subject><subject>Gene Products, gag - metabolism</subject><subject>Gene Products, gag - ultrastructure</subject><subject>Genetic aspects</subject><subject>HIV (Viruses)</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - metabolism</subject><subject>HIV-1 - ultrastructure</subject><subject>Humans</subject><subject>Infectious Diseases</subject><subject>Kinases</subject><subject>Leukemia</subject><subject>Macrophages - metabolism</subject><subject>Membranes</subject><subject>Microscopy, Electron, Transmission</subject><subject>Microtubules - 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metabolism</topic><topic>Biological Transport</topic><topic>Cell Biology</topic><topic>Cell Membrane - metabolism</topic><topic>Cell membranes</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>Endocytosis</topic><topic>Endosomes - metabolism</topic><topic>Gene Products, gag - genetics</topic><topic>Gene Products, gag - metabolism</topic><topic>Gene Products, gag - ultrastructure</topic><topic>Genetic aspects</topic><topic>HIV (Viruses)</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - metabolism</topic><topic>HIV-1 - ultrastructure</topic><topic>Humans</topic><topic>Infectious Diseases</topic><topic>Kinases</topic><topic>Leukemia</topic><topic>Macrophages - metabolism</topic><topic>Membranes</topic><topic>Microscopy, Electron, Transmission</topic><topic>Microtubules - metabolism</topic><topic>Plasma</topic><topic>Proteins</topic><topic>Virion - genetics</topic><topic>Virion - metabolism</topic><topic>Virion - ultrastructure</topic><topic>Virology</topic><topic>Virus Assembly</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jouvenet, Nolwenn</creatorcontrib><creatorcontrib>Neil, Stuart J D</creatorcontrib><creatorcontrib>Bess, Cameron</creatorcontrib><creatorcontrib>Johnson, Marc C</creatorcontrib><creatorcontrib>Virgen, Cesar A</creatorcontrib><creatorcontrib>Simon, Sanford M</creatorcontrib><creatorcontrib>Bieniasz, Paul D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Opposing Viewpoints In Context</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Agriculture & Environmental Science Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - 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Thereafter, late endosome-based secretory pathways are thought to deliver Gag or assembled virions to the plasma membrane (PM) and extracellular milieu. We present several findings that are inconsistent with this model. Specifically, we demonstrate that HIV-1 Gag is delivered to the PM, and virions are efficiently released into the extracellular medium, when late endosome motility is abolished. Furthermore, we show that HIV-1 virions are efficiently released when assembly is rationally targeted to the PM, but not when targeted to late endosomes. Recently synthesized Gag first accumulates and assembles at the PM, but a proportion is subsequently internalized via endocytosis or phagocytosis, thus accounting for observations of endosomal localization. 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subjects | Actins - metabolism Biological Transport Cell Biology Cell Membrane - metabolism Cell membranes Cells, Cultured Cellular biology Endocytosis Endosomes - metabolism Gene Products, gag - genetics Gene Products, gag - metabolism Gene Products, gag - ultrastructure Genetic aspects HIV (Viruses) HIV-1 - genetics HIV-1 - metabolism HIV-1 - ultrastructure Humans Infectious Diseases Kinases Leukemia Macrophages - metabolism Membranes Microscopy, Electron, Transmission Microtubules - metabolism Plasma Proteins Virion - genetics Virion - metabolism Virion - ultrastructure Virology Virus Assembly Viruses |
title | Plasma membrane is the site of productive HIV-1 particle assembly |
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