Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comment
. 2014;9(1):13-6.
doi: 10.2217/fmb.13.141.

How enteric pathogens know they hit the sweet spot

Affiliations
Comment

How enteric pathogens know they hit the sweet spot

Israel Alvarado et al. Future Microbiol. 2014.

Abstract

Ng KM, Ferreyra JA, Higginbottom SK et al. Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens. Nature 502(7469), 96-99 (2013). The human gut microbiota is a complex system of commensal microorganisms required for normal host physiology. Disruption of this protective barrier by antibiotics creates opportunities for enteric pathogens to establish infections. Although the correlation between the use of antibiotics and enteric infections have been known for some time, the specific signals that allow enteric pathogens to recognize a susceptible host have not been determined. In a recent article, Ng et al. demonstrated that the expansion of both Salmonella typhimurium and Clostridium difficile infections is enhanced by the availability of host-specific sugars liberated from the intestinal mucus by commensal bacteria. These results show how antibiotic removal of specific species from the gut microbiome allows symbiotic functions to be hijacked by pathogenic species.

PubMed Disclaimer

Comment on

References

    1. Ng KM, Ferreyra JA, Higginbottom SK et al. Microbiota-liberated host sugars facilitate post-antibiotic expansion of enteric pathogens. Nature 502(7469), 96–99 (2013). - PMC - PubMed
    1. Round JL, Mazmanian SK. The gut microbiota shapes intestinal immune responses during health and disease. Nat. Rev. Immunol 9(5), 313–323 (2009). - PMC - PubMed
    1. Zoetendal E, Rajilić-Stojanović M, de Vos W. High-throughput diversity and functionality analysis of the gastrointestinal tract microbiota. Gut 57(11), 1605–1615 (2008). - PubMed
    1. Nicholson JK, Holmes E, Kinross J et al. Host–gut microbiota metabolic interactions. Science 336(6086), 1262–1267 (2012). - PubMed
    1. Ouwerkerk JP, de Vos WM, Belzer C. Glycobiome: bacteria and mucus at the epithelial interface. Best Pract. Res. Clin. Gastroenterol 27(1), 25–38 (2013). - PubMed

MeSH terms

Substances