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Review
. 2013:2013:237921.
doi: 10.1155/2013/237921. Epub 2013 Mar 13.

The role of cell surface architecture of lactobacilli in host-microbe interactions in the gastrointestinal tract

Affiliations
Review

The role of cell surface architecture of lactobacilli in host-microbe interactions in the gastrointestinal tract

Ranjita Sengupta et al. Mediators Inflamm. 2013.

Abstract

Lactobacillus species can exert health promoting effects in the gastrointestinal tract (GIT) through many mechanisms, which include pathogen inhibition, maintenance of microbial balance, immunomodulation, and enhancement of the epithelial barrier function. Different species of the genus Lactobacillus can evoke different responses in the host, and not all strains of the same species can be considered beneficial. Strain variations may be related to diversity of the cell surface architecture of lactobacilli and the bacteria's ability to express certain surface components or secrete specific compounds in response to the host environment. Lactobacilli are known to modify their surface structures in response to stress factors such as bile and low pH, and these adaptations may help their survival in the face of harsh environmental conditions encountered in the GIT. In recent years, multiple cell surface-associated molecules have been implicated in the adherence of lactobacilli to the GIT lining, immunomodulation, and protective effects on intestinal epithelial barrier function. Identification of the relevant bacterial ligands and their host receptors is imperative for a better understanding of the mechanisms through which lactobacilli exert their beneficial effects on human health.

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Figures

Figure 1
Figure 1
Cell envelope of lactobacilli with a schematic representation of cell-wall and membrane-associated proteins (the figure was adapted from [35, 153]). The bilipidic cell membrane (CM) with embedded proteins is covered by a multilayered peptidoglycan (PG) shell decorated with lipoteichoic acids (LTA), wall teichoic acids (WTA), pili, proteins, and lipoproteins. Exopolysaccharides (EPS) form a thick covering closely associated with PG and are surrounded by an outer envelope of S-layer proteins. The proteins are attached to the cell wall either covalently (LPXTG proteins) or noncovalently (exhibiting LysM, SH3, or WXL domains), lipid anchored to the CM (lipoproteins) or attached to the CM via N- or C-terminal transmembrane helix. M: N-acetyl-muramic acid; G: N-acetyl-glucosamine.

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