Lipopolysaccharide and the gut microbiota: considering structural variation.

gut barrier gut microbiome immunity inflammation lipopolysaccharide binding protein lipopolysaccharide variant lipopolysaccharides metabolic endotoxemia obesity

Journal

FEBS letters
ISSN: 1873-3468
Titre abrégé: FEBS Lett
Pays: England
ID NLM: 0155157

Informations de publication

Date de publication:
04 2022
Historique:
revised: 16 02 2022
received: 29 10 2021
accepted: 17 02 2022
pubmed: 10 3 2022
medline: 14 4 2022
entrez: 9 3 2022
Statut: ppublish

Résumé

Systemic inflammation is associated with chronic disease and is purported to be a main pathogenic mechanism underlying metabolic conditions. Microbes harbored in the host gastrointestinal tract release signaling byproducts from their cell wall, such as lipopolysaccharides (LPS), which can act locally and, after crossing the gut barrier and entering circulation, also systemically. Defined as metabolic endotoxemia, elevated concentrations of LPS in circulation are associated with metabolic conditions and chronic disease. As such, measurement of LPS is highly prevalent in animal and human research investigating these states. Indeed, LPS can be a potent stimulant of host immunity, but this response depends on the microbial species' origin, a parameter often overlooked in both preclinical and clinical investigations. Indeed, the lipid A portion of LPS is mutable and comprises the main virulence and endotoxic component, thus contributing to the structural and functional diversity among LPSs from microbial species. In this review, we discuss how such structural differences in LPS can induce differential immunological responses in the host.

Identifiants

pubmed: 35262962
doi: 10.1002/1873-3468.14328
doi:

Substances chimiques

Endotoxins 0
Lipopolysaccharides 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

849-875

Informations de copyright

© 2022 Federation of European Biochemical Societies.

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Auteurs

Alex E Mohr (AE)

College of Health Solutions, Arizona State University, Phoenix, AZ, USA.

Meli'sa Crawford (M)

Biomedical Sciences, University of Riverside, California, Riverside, CA, USA.

Paniz Jasbi (P)

College of Health Solutions, Arizona State University, Phoenix, AZ, USA.

Samantha Fessler (S)

College of Health Solutions, Arizona State University, Phoenix, AZ, USA.

Karen L Sweazea (KL)

College of Health Solutions, Arizona State University, Phoenix, AZ, USA.
School of Life Sciences, Arizona State University, Tempe, AZ, USA.

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