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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...
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/PMC9352052/ https://www.ncbi.nlm.nih.gov/pubmed/35925870 http://dx.doi.org/10.1371/journal.ppat.1010575 |
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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_facet | 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 | Flomm, Felix J. |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-9352052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-93520522022-08-05 Intermittent bulk release of human cytomegalovirus Flomm, Felix J. Soh, Timothy K. Schneider, Carola Wedemann, Linda Britt, Hannah M. Thalassinos, Konstantinos Pfitzner, Søren Reimer, Rudolph Grünewald, Kay Bosse, Jens B. PLoS Pathog Research Article 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. Public Library of Science 2022-08-04 /pmc/articles/PMC9352052/ /pubmed/35925870 http://dx.doi.org/10.1371/journal.ppat.1010575 Text en © 2022 Flomm 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 Flomm, Felix J. Soh, Timothy K. Schneider, Carola Wedemann, Linda Britt, Hannah M. Thalassinos, Konstantinos Pfitzner, Søren Reimer, Rudolph Grünewald, Kay Bosse, Jens B. Intermittent bulk release of human cytomegalovirus |
title | Intermittent bulk release of human cytomegalovirus |
title_full | Intermittent bulk release of human cytomegalovirus |
title_fullStr | Intermittent bulk release of human cytomegalovirus |
title_full_unstemmed | Intermittent bulk release of human cytomegalovirus |
title_short | Intermittent bulk release of human cytomegalovirus |
title_sort | intermittent bulk release of human cytomegalovirus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352052/ https://www.ncbi.nlm.nih.gov/pubmed/35925870 http://dx.doi.org/10.1371/journal.ppat.1010575 |
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