Antibiotics;
Microbiota;
Microbiome;
OMICS;
HUMAN INTESTINAL MICROBIOTA;
GUT MICROBIOTA;
HEALTHY-VOLUNTEERS;
FECAL MICROBIOTA;
ANTIMICROBIAL RESISTANCE;
CLOSTRIDIUM-DIFFICILE;
COLONIC MICROBIOTA;
GENE-EXPRESSION;
IMPACT;
DIVERSITY;
D O I:
10.1016/j.bcp.2016.09.007
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Our microbiome should be understood as one of the most complex components of the human body. The use of beta-lactam antibiotics is one of the microbiome covariates that influence its composition. The extent to which our microbiota changes after an antibiotic intervention depends not only on the chemical nature of the antibiotic or cocktail of antibiotics used to treat specific infections, but also on the type of administration, duration and dose, as well as the level of resistance that each microbiota develops. We have begun to appreciate that not all bacteria within our microbiota are vulnerable or reactive to different antibiotic interventions, and that their influence on both microbial composition and metabolism may differ. Antibiotics are being used worldwide on a huge scale and the prescription of antibiotics is continuing to rise; however, their effects on our microbiota have been reported for only a limited number of them. This article presents a critical review of the antibiotics or antibiotic cocktails whose use in humans has been linked to changes in the composition of our microbial communities, with a particular focus on the gut, oral, respiratory, skin and vaginal microbiota, and on their molecular agents (genes, proteins and metabolites). We review the state of the art as of June 2016, and cover a total of circa 68 different antibiotics. The data herein are the first to compile information about the bacteria, fungi, archaea and viruses most influenced by the main antibiotic treatments prescribed nowadays. (C) 2016 Elsevier Inc. All rights reserved.
机构:
Washington Univ, Sch Med St Louis, Dept Pediat, Div Infect Dis, St Louis, MO 63110 USA
Washington Univ, Sch Med St Louis, Edison Family Ctr Genome Sci & Syst Biol, St Louis, MO 63110 USAWashington Univ, Sch Med St Louis, Dept Pediat, Div Infect Dis, St Louis, MO 63110 USA
Schwartz, D. J.
Langdon, A. E.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med St Louis, Edison Family Ctr Genome Sci & Syst Biol, St Louis, MO 63110 USA
Washington Univ, Sch Med St Louis, Dept Pathol & Immunol, Div Lab & Genom Med, St Louis, MO 63110 USAWashington Univ, Sch Med St Louis, Dept Pediat, Div Infect Dis, St Louis, MO 63110 USA
Langdon, A. E.
Dantas, G.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med St Louis, Edison Family Ctr Genome Sci & Syst Biol, St Louis, MO 63110 USA
Washington Univ, Sch Med St Louis, Dept Pathol & Immunol, Div Lab & Genom Med, St Louis, MO 63110 USA
Washington Univ St Louis, Dept Biomed Engn, St Louis, MO 63110 USA
Washington Univ, Sch Med St Louis, Dept Mol Microbiol, St Louis, MO 63110 USAWashington Univ, Sch Med St Louis, Dept Pediat, Div Infect Dis, St Louis, MO 63110 USA