1. A tale of two sites: how inflammation can reshape the microbiomes of the gut and lungs.
- Author
-
Scales BS, Dickson RP, and Huffnagle GB
- Subjects
- Anaerobiosis, Colitis immunology, Colitis microbiology, Cystic Fibrosis immunology, Cystic Fibrosis microbiology, Escherichia coli Infections immunology, Feedback, Physiological, Gammaproteobacteria physiology, Gastrointestinal Microbiome, Gastrointestinal Tract immunology, Humans, Inflammation immunology, Inflammation metabolism, Lung immunology, Mucus metabolism, Nitric Oxide metabolism, Nitric Oxide Synthase Type II metabolism, Nitrogen metabolism, Oxidation-Reduction, Pseudomonas Infections immunology, Gastrointestinal Tract microbiology, Inflammation microbiology, Lung microbiology, Microbiota immunology
- Abstract
Inflammation can directly and indirectly modulate the bacterial composition of the microbiome. Although studies of inflammation primarily focus on its function to negatively select against potential pathogens, some bacterial species have the ability to exploit inflammatory byproducts for their benefit. Inflammatory cells release reactive nitrogen species as antimicrobial effectors against infection, but some facultative anaerobes can also utilize the increase in extracellular nitrate in their environment for anaerobic respiration and growth. This phenomenon has been studied in the gastrointestinal tract, where blooms of facultative anaerobic Gammaproteobacteria, primarily Escherichia coli, often occur during colonic inflammation. In cystic fibrosis, Pseudomonas aeruginosa, another Gammaproteobacteria facultative anaerobe, can reduce nitrogen for anaerobic respiration and it blooms in the airways of the chronically inflamed cystic fibrosis lung. This review focuses on the evidence that inflammation can provide terminal electron acceptors for anaerobic respiration and can support blooms of facultative anaerobes, such as E. coli and P. aeruginosa in distinct, but similar, environments of the inflamed gastrointestinal and respiratory tracts., (© Society for Leukocyte Biology.)
- Published
- 2016
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