Intermittent bulk release of human cytomegalovirus
Human Cytomegalovirus (HCMV) can infect a variety of cell types by using virions of varying glycoprotein compositions. It is still unclear how this diversity is generated, but spatio-temporally separated envelopment and egress pathways might play a role. So far, one egress pathway has been described...
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description | Human Cytomegalovirus (HCMV) can infect a variety of cell types by using virions of varying glycoprotein compositions. It is still unclear how this diversity is generated, but spatio-temporally separated envelopment and egress pathways might play a role. So far, one egress pathway has been described in which HCMV particles are individually enveloped into small vesicles and are subsequently exocytosed continuously. However, some studies have also found enveloped virus particles inside multivesicular structures but could not link them to productive egress or degradation pathways. We used a novel 3D-CLEM workflow allowing us to investigate these structures in HCMV morphogenesis and egress at high spatio-temporal resolution. We found that multiple envelopment events occurred at individual vesicles leading to multiviral bodies (MViBs), which subsequently traversed the cytoplasm to release virions as intermittent bulk pulses at the plasma membrane to form extracellular virus accumulations (EVAs). Our data support the existence of a novel bona fide HCMV egress pathway, which opens the gate to evaluate divergent egress pathways in generating virion diversity. |
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It is still unclear how this diversity is generated, but spatio-temporally separated envelopment and egress pathways might play a role. So far, one egress pathway has been described in which HCMV particles are individually enveloped into small vesicles and are subsequently exocytosed continuously. However, some studies have also found enveloped virus particles inside multivesicular structures but could not link them to productive egress or degradation pathways. We used a novel 3D-CLEM workflow allowing us to investigate these structures in HCMV morphogenesis and egress at high spatio-temporal resolution. We found that multiple envelopment events occurred at individual vesicles leading to multiviral bodies (MViBs), which subsequently traversed the cytoplasm to release virions as intermittent bulk pulses at the plasma membrane to form extracellular virus accumulations (EVAs). Our data support the existence of a novel bona fide HCMV egress pathway, which opens the gate to evaluate divergent egress pathways in generating virion diversity.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1010575</identifier><identifier>PMID: 35925870</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Artificial chromosomes ; Biology and Life Sciences ; Biosynthesis ; Composition ; Cytomegalovirus ; Cytomegaloviruses ; Cytoplasm ; Cytoplasm - metabolism ; Egress ; Fibroblasts ; Glycoproteins ; Growth ; Humans ; Infections ; Medicine and Health Sciences ; Membranes ; Microscopy ; Morphogenesis ; Mutation ; Physiological aspects ; Plasma ; Proteins ; Structure ; Temporal resolution ; Vaccines ; Vesicles ; Viral proteins ; Virion ; Virions ; Virus Assembly ; Viruses ; Workflow</subject><ispartof>PLoS pathogens, 2022-08, Vol.18 (8), p.e1010575</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Flomm et al. 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Our data support the existence of a novel bona fide HCMV egress pathway, which opens the gate to evaluate divergent egress pathways in generating virion diversity.</description><subject>Artificial chromosomes</subject><subject>Biology and Life Sciences</subject><subject>Biosynthesis</subject><subject>Composition</subject><subject>Cytomegalovirus</subject><subject>Cytomegaloviruses</subject><subject>Cytoplasm</subject><subject>Cytoplasm - metabolism</subject><subject>Egress</subject><subject>Fibroblasts</subject><subject>Glycoproteins</subject><subject>Growth</subject><subject>Humans</subject><subject>Infections</subject><subject>Medicine and Health Sciences</subject><subject>Membranes</subject><subject>Microscopy</subject><subject>Morphogenesis</subject><subject>Mutation</subject><subject>Physiological aspects</subject><subject>Plasma</subject><subject>Proteins</subject><subject>Structure</subject><subject>Temporal resolution</subject><subject>Vaccines</subject><subject>Vesicles</subject><subject>Viral proteins</subject><subject>Virion</subject><subject>Virions</subject><subject>Virus Assembly</subject><subject>Viruses</subject><subject>Workflow</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsI_QBCJSy-7-COO7QtSVVFYqRIXOFtjZ7zN4sSLnVTqv6-XTasWcbGt8Zs3741eVb2nZE25pJ93cU4jhPV-D9OaEkqEFC-qUyoEX0kum5dP3ifVm5x3hDSU0_Z1dcKFZkJJclqxzThhGvppwnGq7Rx-1wkDQsY6-vpmHmCs3d0UB9xCiLd9mvPb6pWHkPHdcp9Vv66-_rz8vrr-8W1zeXG9ckI000pTxX2DQqFqO-KsaFF75aV1YK1uibRK-M61zKO3wIqwjnirQZeD-w75WfXxyLsPMZvFbjZMUkEbJkhbEJsjoouwM_vUD5DuTITe_C3EtDWQpt4FNGARlUbloXENdFz5RvCOcd3xUgJSuL4s02Y7YOfKOhKEZ6TPf8b-xmzjrdFcMCJYIThfCFL8M2OezNBnhyHAiHEuulutWk4k0wX66R_o_90tqLJ5NP3oY5nrDqTmoqA0l4wcdDdHlEsx54T-UTIl5hCUB25zCIpZglLaPjy1-9j0kAx-D2EFvKk</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Flomm, Felix J</creator><creator>Soh, Timothy K</creator><creator>Schneider, Carola</creator><creator>Wedemann, Linda</creator><creator>Britt, Hannah M</creator><creator>Thalassinos, Konstantinos</creator><creator>Pfitzner, Søren</creator><creator>Reimer, Rudolph</creator><creator>Grünewald, Kay</creator><creator>Bosse, Jens B</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>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>AEUYN</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>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7252-5541</orcidid></search><sort><creationdate>20220801</creationdate><title>Intermittent bulk release of human cytomegalovirus</title><author>Flomm, Felix J ; Soh, Timothy K ; Schneider, Carola ; Wedemann, Linda ; Britt, Hannah M ; Thalassinos, Konstantinos ; Pfitzner, Søren ; Reimer, Rudolph ; Grünewald, Kay ; Bosse, Jens B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c554t-9183f4e58e86d0cb56e9f8f7bcabb9607b85fdc62fefba2316d0fb9a9fb93fde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Artificial chromosomes</topic><topic>Biology and Life Sciences</topic><topic>Biosynthesis</topic><topic>Composition</topic><topic>Cytomegalovirus</topic><topic>Cytomegaloviruses</topic><topic>Cytoplasm</topic><topic>Cytoplasm - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flomm, Felix J</au><au>Soh, Timothy K</au><au>Schneider, Carola</au><au>Wedemann, Linda</au><au>Britt, Hannah M</au><au>Thalassinos, Konstantinos</au><au>Pfitzner, Søren</au><au>Reimer, Rudolph</au><au>Grünewald, Kay</au><au>Bosse, Jens B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intermittent bulk release of human cytomegalovirus</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>18</volume><issue>8</issue><spage>e1010575</spage><pages>e1010575-</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Human Cytomegalovirus (HCMV) can infect a variety of cell types by using virions of varying glycoprotein compositions. It is still unclear how this diversity is generated, but spatio-temporally separated envelopment and egress pathways might play a role. So far, one egress pathway has been described in which HCMV particles are individually enveloped into small vesicles and are subsequently exocytosed continuously. However, some studies have also found enveloped virus particles inside multivesicular structures but could not link them to productive egress or degradation pathways. We used a novel 3D-CLEM workflow allowing us to investigate these structures in HCMV morphogenesis and egress at high spatio-temporal resolution. We found that multiple envelopment events occurred at individual vesicles leading to multiviral bodies (MViBs), which subsequently traversed the cytoplasm to release virions as intermittent bulk pulses at the plasma membrane to form extracellular virus accumulations (EVAs). Our data support the existence of a novel bona fide HCMV egress pathway, which opens the gate to evaluate divergent egress pathways in generating virion diversity.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35925870</pmid><doi>10.1371/journal.ppat.1010575</doi><orcidid>https://orcid.org/0000-0001-7252-5541</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Artificial chromosomes Biology and Life Sciences Biosynthesis Composition Cytomegalovirus Cytomegaloviruses Cytoplasm Cytoplasm - metabolism Egress Fibroblasts Glycoproteins Growth Humans Infections Medicine and Health Sciences Membranes Microscopy Morphogenesis Mutation Physiological aspects Plasma Proteins Structure Temporal resolution Vaccines Vesicles Viral proteins Virion Virions Virus Assembly Viruses Workflow |
title | Intermittent bulk release of human cytomegalovirus |
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