Drivers and Distribution of Henipavirus-Induced Syncytia: What Do We Know?


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
02 09 2021
Historique:
received: 01 07 2021
revised: 21 08 2021
accepted: 25 08 2021
entrez: 28 9 2021
pubmed: 29 9 2021
medline: 12 2 2022
Statut: epublish

Résumé

Syncytium formation, i.e., cell-cell fusion resulting in the formation of multinucleated cells, is a hallmark of infection by paramyxoviruses and other pathogenic viruses. This natural mechanism has historically been a diagnostic marker for paramyxovirus infection in vivo and is now widely used for the study of virus-induced membrane fusion in vitro. However, the role of syncytium formation in within-host dissemination and pathogenicity of viruses remains poorly understood. The diversity of henipaviruses and their wide host range and tissue tropism make them particularly appropriate models with which to characterize the drivers of syncytium formation and the implications for virus fitness and pathogenicity. Based on the henipavirus literature, we summarized current knowledge on the mechanisms driving syncytium formation, mostly acquired from in vitro studies, and on the in vivo distribution of syncytia. While these data suggest that syncytium formation widely occurs across henipaviruses, hosts, and tissues, we identified important data gaps that undermined our understanding of the role of syncytium formation in virus pathogenesis. Based on these observations, we propose solutions of varying complexity to fill these data gaps, from better practices in data archiving and publication for in vivo studies, to experimental approaches in vitro.

Identifiants

pubmed: 34578336
pii: v13091755
doi: 10.3390/v13091755
pmc: PMC8472861
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : T32GM008185-33
Pays : United States
Organisme : NIH HHS
ID : R01AI109022
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI109022
Pays : United States
Organisme : NIH HHS
ID : R21AI142377
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI142377
Pays : United States

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Auteurs

Amandine Gamble (A)

Department of Ecology & Evolutionary Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

Yao Yu Yeo (YY)

Department of Microbiology & Immunology, Cornell University, Ithaca, NY 14850, USA.

Aubrey A Butler (AA)

Department of Ecology & Evolutionary Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

Hubert Tang (H)

Department of Ecology & Evolutionary Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

Celine E Snedden (CE)

Department of Ecology & Evolutionary Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

Christian T Mason (CT)

Department of Computational Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA.

David W Buchholz (DW)

Department of Microbiology & Immunology, Cornell University, Ithaca, NY 14850, USA.

John Bingham (J)

CSIRO Australian Centre for Disease Preparedness, Geelong, VIC 3220, Australia.

Hector C Aguilar (HC)

Department of Microbiology & Immunology, Cornell University, Ithaca, NY 14850, USA.

James O Lloyd-Smith (JO)

Department of Ecology & Evolutionary Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

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