The intestinal microbiota: Antibiotics, colonization resistance, and enteric pathogens.

TitleThe intestinal microbiota: Antibiotics, colonization resistance, and enteric pathogens.
Publication TypeJournal Article
Year of Publication2017
AuthorsKim S, Covington A, Pamer EG
JournalImmunol Rev
Volume279
Issue1
Pagination90-105
Date Published2017 Sep
ISSN1600-065X
KeywordsAnimals, Anti-Bacterial Agents, Bacterial Infections, Cross Infection, Drug Resistance, Dysbiosis, Gastrointestinal Microbiome, Host-Pathogen Interactions, Humans, Immunocompromised Host
Abstract

The human gastrointestinal tract hosts a diverse network of microorganisms, collectively known as the microbiota that plays an important role in health and disease. For instance, the intestinal microbiota can prevent invading microbes from colonizing the gastrointestinal tract, a phenomenon known as colonization resistance. Perturbations to the microbiota, such as antibiotic administration, can alter microbial composition and result in the loss of colonization resistance. Consequently, the host may be rendered susceptible to colonization by a pathogen. This is a particularly relevant concern in the hospital setting, where antibiotic use and antibiotic-resistant pathogen exposure are more frequent. Many nosocomial infections arise from gastrointestinal colonization. Due to their resistance to antibiotics, treatment is often very challenging. However, recent studies have demonstrated that manipulating the commensal microbiota can prevent and treat various infections in the intestine. In this review, we discuss the members of the microbiota, as well as the mechanisms, that govern colonization resistance against specific pathogens. We also review the effects of antibiotics on the microbiota, as well as the unique epidemiology of immunocompromised patients that renders them a particularly high-risk population to intestinal nosocomial infections.

DOI10.1111/imr.12563
Alternate JournalImmunol. Rev.
PubMed ID28856737
PubMed Central IDPMC6026851
Grant ListU01 AI124275 / AI / NIAID NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R01 AI095706 / AI / NIAID NIH HHS / United States
R01 AI042135 / AI / NIAID NIH HHS / United States
T32 GM007739 / GM / NIGMS NIH HHS / United States