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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Veröffentlicht in:PLoS pathogens 2022-08, Vol.18 (8), p.e1010575
Hauptverfasser: Flomm, Felix J, Soh, Timothy K, Schneider, Carola, Wedemann, Linda, Britt, Hannah M, Thalassinos, Konstantinos, Pfitzner, Søren, Reimer, Rudolph, Grünewald, Kay, Bosse, Jens B
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container_issue 8
container_start_page e1010575
container_title PLoS pathogens
container_volume 18
creator Flomm, Felix J
Soh, Timothy K
Schneider, Carola
Wedemann, Linda
Britt, Hannah M
Thalassinos, Konstantinos
Pfitzner, Søren
Reimer, Rudolph
Grünewald, Kay
Bosse, Jens B
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.
doi_str_mv 10.1371/journal.ppat.1010575
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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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