Restriction of Human Cytomegalovirus Infection by Galectin-9.


Journal

Journal of virology
ISSN: 1098-5514
Titre abrégé: J Virol
Pays: United States
ID NLM: 0113724

Informations de publication

Date de publication:
01 02 2019
Historique:
received: 03 10 2018
accepted: 31 10 2018
pubmed: 30 11 2018
medline: 9 11 2019
entrez: 30 11 2018
Statut: epublish

Résumé

Human cytomegalovirus (HCMV) is a ubiquitous human herpesvirus. While HCMV infection is generally asymptomatic in the immunocompetent, it can have devastating consequences in those with compromised or underdeveloped immune systems, including transplant recipients and neonates. Galectins are a widely expressed protein family that have been demonstrated to modulate both antiviral immunity and regulate direct host-virus interactions. The potential for galectins to directly modulate HCMV infection has not previously been studied, and our results reveal that galectin-9 (Gal-9) can potently inhibit HCMV infection. Gal-9-mediated inhibition of HCMV was dependent upon its carbohydrate recognition domains and thus dependent on glycan interactions. Temperature shift studies revealed that Gal-9 specific inhibition was mediated primarily at the level of virus-cell fusion and not binding. Additionally, we found that during reactivation of HCMV in hematopoietic stem cell transplant (HSCT) patients soluble Gal-9 is upregulated. This study provides the first evidence for Gal-9 functioning as a potent antiviral defense effector molecule against HCMV infection and identifies it as a potential clinical candidate to restrict HCMV infections.

Identifiants

pubmed: 30487283
pii: JVI.01746-18
doi: 10.1128/JVI.01746-18
pmc: PMC6340044
pii:
doi:

Substances chimiques

Antiviral Agents 0
Galectins 0
LGALS9 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2019 American Society for Microbiology.

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Auteurs

Emily A Machala (EA)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia.

Selmir Avdic (S)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia.

Lauren Stern (L)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia.

Dirk M Zajonc (DM)

Division of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, USA.
Department of Internal Medicine Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Chris A Benedict (CA)

Division of Immune Regulation, La Jolla Institute for Allergy and Immunology, La Jolla, California, USA.

Emily Blyth (E)

Westmead Institute for Medical Research, University of Sydney, Westmead, Australia.
Sydney Medical School, University of Sydney, Camperdown, New South Wales, Australia.
Department of Haematology, Westmead Hospital, Sydney, Australia.
Sydney Cellular Therapies Laboratory, Westmead, Australia.

David J Gottlieb (DJ)

Westmead Institute for Medical Research, University of Sydney, Westmead, Australia.
Sydney Medical School, University of Sydney, Camperdown, New South Wales, Australia.
Department of Haematology, Westmead Hospital, Sydney, Australia.
Sydney Cellular Therapies Laboratory, Westmead, Australia.

Allison Abendroth (A)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia.

Brian P McSharry (BP)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia.

Barry Slobedman (B)

Discipline of Infectious Diseases and Immunology, University of Sydney, Camperdown, New South Wales, Australia barry.slobedman@sydney.edu.au.

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