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Antibiotic-induced changes in the microbiota disrupt redox dynamics in the gut.
Reese, Aspen T; Cho, Eugenia H; Klitzman, Bruce; Nichols, Scott P; Wisniewski, Natalie A; Villa, Max M; Durand, Heather K; Jiang, Sharon; Midani, Firas S; Nimmagadda, Sai N; O'Connell, Thomas M; Wright, Justin P; Deshusses, Marc A; David, Lawrence A.
Afiliación
  • Reese AT; Department of Biology, Duke University, Durham, United States.
  • Cho EH; Department of Molecular Genetics and Microbiology, Duke University, Durham, United States.
  • Klitzman B; Department of Bioengineering, University of Pennsylvania, Philadelphia, United States.
  • Nichols SP; Department of Surgery, Duke University Medical Center, Durham, United States.
  • Wisniewski NA; Profusa, Inc., South San Francisco, United States.
  • Villa MM; Profusa, Inc., South San Francisco, United States.
  • Durand HK; Department of Molecular Genetics and Microbiology, Duke University, Durham, United States.
  • Jiang S; Department of Molecular Genetics and Microbiology, Duke University, Durham, United States.
  • Midani FS; Department of Molecular Genetics and Microbiology, Duke University, Durham, United States.
  • Nimmagadda SN; Program in Computational Biology and Bioinformatics, Duke University, Durham, United States.
  • O'Connell TM; Department of Biomedical Engineering, Duke University, Durham, United States.
  • Wright JP; Department of Otolaryngology-Head and Neck Surgery, Indiana University School of Medicine, Indianapolis, United States.
  • Deshusses MA; Department of Biology, Duke University, Durham, United States.
  • David LA; Department of Civil and Environmental Engineering, Duke University, Durham, United States.
Elife ; 72018 06 19.
Article en En | MEDLINE | ID: mdl-29916366
How host and microbial factors combine to structure gut microbial communities remains incompletely understood. Redox potential is an important environmental feature affected by both host and microbial actions. We assessed how antibiotics, which can impact host and microbial function, change redox state and how this contributes to post-antibiotic succession. We showed gut redox potential increased within hours of an antibiotic dose in mice. Host and microbial functioning changed under treatment, but shifts in redox potentials could be attributed specifically to bacterial suppression in a host-free ex vivo human gut microbiota model. Redox dynamics were linked to blooms of the bacterial family Enterobacteriaceae. Ecological succession to pre-treatment composition was associated with recovery of gut redox, but also required dispersal from unaffected gut communities. As bacterial competition for electron acceptors can be a key ecological factor structuring gut communities, these results support the potential for manipulating gut microbiota through managing bacterial respiration.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tracto Gastrointestinal / Enterobacteriaceae / Microbioma Gastrointestinal / Antibacterianos Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tracto Gastrointestinal / Enterobacteriaceae / Microbioma Gastrointestinal / Antibacterianos Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article