Back to Search
Start Over
The role of cell surface architecture of lactobacilli in host-microbe interactions in the gastrointestinal tract
- Source :
- Mediators of Inflammation, Mediators of Inflammation, Vol 2013 (2013)
- Publication Year :
- 2012
-
Abstract
- Lactobacillusspecies 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 genusLactobacilluscan 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.
- Subjects :
- Gastrointestinal tract
biology
Host (biology)
Probiotics
Immunology
Cell
food and beverages
Cell Biology
Review Article
biology.organism_classification
Bacterial Adhesion
Microbiology
Gastrointestinal Tract
Lactobacillus
medicine.anatomical_structure
medicine
lcsh:Pathology
Humans
Secretion
Receptor
Pathogen
Bacteria
lcsh:RB1-214
Subjects
Details
- ISSN :
- 14661861
- Volume :
- 2013
- Database :
- OpenAIRE
- Journal :
- Mediators of inflammation
- Accession number :
- edsair.doi.dedup.....cb3bd3db000c9c75dbca32e35ba7f818