The Role of Gut Dysbiosis in the Loss of Intestinal Immune Cell Functions and Viral Pathogenesis.

FMT gut dysbiosis probiotics viral pathogenesis γδ T cell

Journal

Microorganisms
ISSN: 2076-2607
Titre abrégé: Microorganisms
Pays: Switzerland
ID NLM: 101625893

Informations de publication

Date de publication:
21 Jul 2023
Historique:
received: 08 06 2023
revised: 15 07 2023
accepted: 20 07 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

The gut microbiome plays a critical role in maintaining overall health and immune function. However, dysbiosis, an imbalance in microbiome composition, can have profound effects on various aspects of human health, including susceptibility to viral infections. Despite numerous studies investigating the influence of viral infections on gut microbiome, the impact of gut dysbiosis on viral infection and pathogenesis remains relatively understudied. The clinical variability observed in SARS-CoV-2 and seasonal influenza infections, and the presence of natural HIV suppressors, suggests that host-intrinsic factors, including the gut microbiome, may contribute to viral pathogenesis. The gut microbiome has been shown to influence the host immune system by regulating intestinal homeostasis through interactions with immune cells. This review aims to enhance our understanding of how viral infections perturb the gut microbiome and mucosal immune cells, affecting host susceptibility and response to viral infections. Specifically, we focus on exploring the interactions between gamma delta (γδ) T cells and gut microbes in the context of inflammatory viral pathogenesis and examine studies highlighting the role of the gut microbiome in viral disease outcomes. Furthermore, we discuss emerging evidence and potential future directions for microbiome modulation therapy in the context of viral pathogenesis.

Identifiants

pubmed: 37513022
pii: microorganisms11071849
doi: 10.3390/microorganisms11071849
pmc: PMC10384393
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : NIAAA NIH HHS
ID : P60 AA009803
Pays : United States

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Auteurs

Farzaneh Fakharian (F)

Department of Microbiology, Faculty of Biological Sciences and Technology, Shahid Beheshti University, Tehran 1983969411, Iran.

Siva Thirugnanam (S)

Tulane National Primate Research Center, Covington, LA 70433, USA.
Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA 70112, USA.

David A Welsh (DA)

Department of Microbiology, Immunology and Parasitology, Louisiana State University School of Medicine, New Orleans, LA 70806, USA.

Woong-Ki Kim (WK)

Tulane National Primate Research Center, Covington, LA 70433, USA.
Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA 70112, USA.

Jay Rappaport (J)

Tulane National Primate Research Center, Covington, LA 70433, USA.

Kyle Bittinger (K)

Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Namita Rout (N)

Tulane National Primate Research Center, Covington, LA 70433, USA.
Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Tulane Center for Aging, Tulane University School of Medicine, New Orleans, LA 70112, USA.

Classifications MeSH