The Intestinal Microbiota: Impacts of Antibiotics Therapy, Colonization Resistance, and Diseases

Int J Mol Sci. 2021 Jun 20;22(12):6597. doi: 10.3390/ijms22126597.

Abstract

Trillions of microbes exist in the human body, particularly the gastrointestinal tract, coevolved with the host in a mutually beneficial relationship. The main role of the intestinal microbiome is the fermentation of non-digestible substrates and increased growth of beneficial microbes that produce key antimicrobial metabolites such as short-chain fatty acids, etc., to inhibit the growth of pathogenic microbes besides other functions. Intestinal microbiota can prevent pathogen colonization through the mechanism of colonization resistance. A wide range of resistomes are present in both beneficial and pathogenic microbes. Giving antibiotic exposure to the intestinal microbiome (both beneficial and hostile) can trigger a resistome response, affecting colonization resistance. The following review provides a mechanistic overview of the intestinal microbiome and the impacts of antibiotic therapy on pathogen colonization and diseases. Further, we also discuss the epidemiology of immunocompromised patients who are at high risk for nosocomial infections, colonization and decolonization of multi-drug resistant organisms in the intestine, and the direct and indirect mechanisms that govern colonization resistance to the pathogens.

Keywords: antibiotics; colonization resistance; diseases; intestinal microbiota; pathogens.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Anti-Infective Agents / pharmacology
  • Anti-Infective Agents / therapeutic use
  • Antibiosis*
  • Antimicrobial Cationic Peptides / pharmacology
  • Antimicrobial Cationic Peptides / therapeutic use
  • Cross Infection / drug therapy
  • Cross Infection / etiology
  • Disease Susceptibility*
  • Drug Resistance, Multiple
  • Gastrointestinal Microbiome* / drug effects
  • Host-Pathogen Interactions*
  • Humans
  • Sepsis / etiology

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Antimicrobial Cationic Peptides