Unknown

Dataset Information

0

Gut microbiota. Antimicrobial peptide resistance mediates resilience of prominent gut commensals during inflammation.


ABSTRACT: Resilience to host inflammation and other perturbations is a fundamental property of gut microbial communities, yet the underlying mechanisms are not well understood. We have found that human gut microbes from all dominant phyla are resistant to high levels of inflammation-associated antimicrobial peptides (AMPs) and have identified a mechanism for lipopolysaccharide (LPS) modification in the phylum Bacteroidetes that increases AMP resistance by four orders of magnitude. Bacteroides thetaiotaomicron mutants that fail to remove a single phosphate group from their LPS were displaced from the microbiota during inflammation triggered by pathogen infection. These findings establish a mechanism that determines the stability of prominent members of a healthy microbiota during perturbation.

SUBMITTER: Cullen TW 

PROVIDER: S-EPMC4388331 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Gut microbiota. Antimicrobial peptide resistance mediates resilience of prominent gut commensals during inflammation.

Cullen T W TW   Schofield W B WB   Barry N A NA   Putnam E E EE   Rundell E A EA   Trent M S MS   Degnan P H PH   Booth C J CJ   Yu H H   Goodman A L AL  

Science (New York, N.Y.) 20150101 6218


Resilience to host inflammation and other perturbations is a fundamental property of gut microbial communities, yet the underlying mechanisms are not well understood. We have found that human gut microbes from all dominant phyla are resistant to high levels of inflammation-associated antimicrobial peptides (AMPs) and have identified a mechanism for lipopolysaccharide (LPS) modification in the phylum Bacteroidetes that increases AMP resistance by four orders of magnitude. Bacteroides thetaiotaomi  ...[more]

Similar Datasets

| S-EPMC7870933 | biostudies-literature
| S-EPMC6387620 | biostudies-literature
| S-EPMC4820042 | biostudies-literature
2024-01-16 | GSE250268 | GEO
2023-12-04 | GSE248940 | GEO
2024-02-28 | GSE229566 | GEO
| S-EPMC4855262 | biostudies-other
| PRJEB7688 | ENA
| PRJEB7697 | ENA
| S-EPMC4824762 | biostudies-literature