Epithelial-Derived Reactive Oxygen Species Enable AppBCX-Mediated Aerobic Respiration of Escherichia coli during Intestinal Inflammation

Autor: Lisa Büttner, Wenhan Zhu, Rachael B. Chanin, Madeline P. Smoot, Angel G. Jimenez, Sebastian E. Winter, Savannah J. Taylor, Luisella Spiga, Caroline C. Gillis, Renato L. Santos, Alexandre Arenales, Maria G. Winter, Elizabeth R. Hughes
Rok vydání: 2020
Předmět:
gut microbiota dysbiosis
Male
Microbial metabolism
Inbred C57BL
Mice
0302 clinical medicine
Intestinal Mucosa
Inbred BALB C
chemistry.chemical_classification
reactive oxygen species
0303 health sciences
Oxidase test
Mice
Inbred BALB C

Escherichia coli Proteins
Microbiota
Bacterial
NADPH Oxidase 1
Colitis
Aerobiosis
Infectious Diseases
Medical Microbiology
NOX1
Female
gut inflammation
Infection
DNA
Bacterial

Cellular respiration
Immunology
Biology
Autoimmune Disease
Microbiology
Article
Electron Transport Complex IV
03 medical and health sciences
microbial respiration
Virology
Genetic model
Escherichia coli
Cytochrome c oxidase
Animals
intestinal epithelium
030304 developmental biology
Inflammation
Reactive oxygen species
Host Microbial Interactions
Animal
Prevention
Inflammatory Bowel Disease
DNA
cytochrome oxidase
Hydrogen Peroxide
Gastrointestinal Microbiome
Mice
Inbred C57BL

Oxygen
Disease Models
Animal

Good Health and Well Being
chemistry
Disease Models
biology.protein
Parasitology
Digestive Diseases
Reactive Oxygen Species
030217 neurology & neurosurgery
Zdroj: Cell Host Microbe
Cell host & microbe, vol 28, iss 6
ISSN: 1934-6069
Popis: The intestinal epithelium separates host tissue and gut-associated microbial communities. During inflammation, the host releases reactive oxygen and nitrogen species as an antimicrobial response. The impact of these radicals on gut microbes is incompletely understood. We discovered that the cryptic appBCX genes, predicted to encode a cytochrome bd-II oxidase, conferred a fitness advantage for E.coli in chemical and genetic models of non-infectious colitis. This fitness advantage was absent in mice that lacked epithelial NADPH oxidase 1 (NOX1) activity. In laboratory growth experiments, supplementation with exogenous hydrogen peroxide enhanced E.coli growth through AppBCX-mediated respiration in a catalase-dependent manner. We conclude that epithelial-derived reactive oxygen species are degraded in the gut lumen, which gives rise to molecular oxygen that supports the aerobic respiration of E.coli. This work illustrates how epithelial host responses intersect with gut microbial metabolism in the context of gut inflammation.
Databáze: OpenAIRE