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Dryad

Intermittent bulk release of human cytomegalovirus: associated data

Cite this dataset

Flomm, Felix et al. (2022). Intermittent bulk release of human cytomegalovirus: associated data [Dataset]. Dryad. https://doi.org/10.5061/dryad.gtht76hpt

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.

Methods

Details on data acquisition and processing can be found in the original publication.

Usage notes

Some microscopy raw data are in the proprietary format of the microscope manufacturer. However, all files can be opened with an up-to-date version of Fiji/ImageJ, using the BioFormats importer.

Funding

Wellcome Trust, Award: 209250/Z/17/Z

Deutsche Forschungsgemeinschaft, Award: 390874280

Deutsche Forschungsgemeinschaft, Award: 413831413

German National Academic Foundation

Deutsche Forschungsgemeinschaft, Award: BO 4158/5-1

Freie und Hansestadt Hamburg, Award: LFF-FV 71-2019

Leibniz Association, Award: W6/2018

Wellcome Trust, Award: 104913/Z/14/Z