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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...

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Autores principales: Flomm, Felix J., Soh, Timothy K., Schneider, Carola, Wedemann, Linda, Britt, Hannah M., Thalassinos, Konstantinos, Pfitzner, Søren, Reimer, Rudolph, Grünewald, Kay, Bosse, Jens B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
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.
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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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