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Antibiotic-Induced Changes to the Host Metabolic Environment Inhibit Drug Efficacy and Alter Immune Function

Authors :
Institute for Medical Engineering and Science
Massachusetts Institute of Technology. Department of Biological Engineering
Yang, Jason Hung-Ying
Saluja, Prerna Bhargava
Mao, Ning
Collins, James J.
McCloskey, Douglas
Palsson, Bernhard O.
Institute for Medical Engineering and Science
Massachusetts Institute of Technology. Department of Biological Engineering
Yang, Jason Hung-Ying
Saluja, Prerna Bhargava
Mao, Ning
Collins, James J.
McCloskey, Douglas
Palsson, Bernhard O.
Source :
PMC
Publication Year :
2019

Abstract

Bactericidal antibiotics alter microbial metabolism as part of their lethality and can damage mitochondria in mammalian cells. In addition, antibiotic susceptibility is sensitive to extracellular metabolites, but it remains unknown whether metabolites present at an infection site can affect either treatment efficacy or immune function. Here, we quantify local metabolic changes in the host microenvironment following antibiotic treatment for a peritoneal Escherichia coli infection. Antibiotic treatment elicits microbiome-independent changes in local metabolites, but not those distal to the infection site, by acting directly on host cells. The metabolites induced during treatment, such as AMP, reduce antibiotic efficacy and enhance phagocytic killing. Moreover, antibiotic treatment impairs immune function by inhibiting respiratory activity in immune cells. Collectively, these results highlight the immunomodulatory potential of antibiotics and reveal the local metabolic microenvironment to be an important determinant of infection resolution. Antibiotic susceptibility is sensitive to metabolites, but how this affects in vivo treatment efficacy remains unexplored. Yang, Bhargava et al. characterize antibiotic-induced changes to the metabolic environment during infection and find that direct actions of antibiotics on host cells induce metabolites that impair drug efficacy and enhance phagocytic activity.<br />United States. Defense Threat Reduction Agency (Grant HDTRA1-15-1-0051)<br />National Institutes of Health (U.S.) (Grant U01AI124316)<br />National Institutes of Health (U.S.) (Grant K99GM118907)<br />Novo Nordisk Foundation (Grant NNF16CC0021858)<br />Paul G. Allen Frontiers Group<br />Wyss Institute for Biologically Inspired Engineering

Details

Database :
OAIster
Journal :
PMC
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1141888898
Document Type :
Electronic Resource