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Extensive impact of non-antibiotic drugs on human gut bacteria.
Maier, Lisa; Pruteanu, Mihaela; Kuhn, Michael; Zeller, Georg; Telzerow, Anja; Anderson, Exene Erin; Brochado, Ana Rita; Fernandez, Keith Conrad; Dose, Hitomi; Mori, Hirotada; Patil, Kiran Raosaheb; Bork, Peer; Typas, Athanasios.
Afiliação
  • Maier L; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Pruteanu M; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Kuhn M; European Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117 Heidelberg, Germany.
  • Zeller G; European Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117 Heidelberg, Germany.
  • Telzerow A; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Anderson EE; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Brochado AR; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Fernandez KC; European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
  • Dose H; Graduate School of Biological Sciences, Nara Institute of Science and Technology, 630-0101 Ikoma, Japan.
  • Mori H; Graduate School of Biological Sciences, Nara Institute of Science and Technology, 630-0101 Ikoma, Japan.
  • Patil KR; European Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117 Heidelberg, Germany.
  • Bork P; European Molecular Biology Laboratory, Structural and Computational Biology Unit, 69117 Heidelberg, Germany.
  • Typas A; Max-Delbrück-Centre for Molecular Medicine, 13125 Berlin, Germany.
Nature ; 555(7698): 623-628, 2018 03 29.
Article em En | MEDLINE | ID: mdl-29555994
ABSTRACT
A few commonly used non-antibiotic drugs have recently been associated with changes in gut microbiome composition, but the extent of this phenomenon is unknown. Here, we screened more than 1,000 marketed drugs against 40 representative gut bacterial strains, and found that 24% of the drugs with human targets, including members of all therapeutic classes, inhibited the growth of at least one strain in vitro. Particular classes, such as the chemically diverse antipsychotics, were overrepresented in this group. The effects of human-targeted drugs on gut bacteria are reflected on their antibiotic-like side effects in humans and are concordant with existing human cohort studies. Susceptibility to antibiotics and human-targeted drugs correlates across bacterial species, suggesting common resistance mechanisms, which we verified for some drugs. The potential risk of non-antibiotics promoting antibiotic resistance warrants further exploration. Our results provide a resource for future research on drug-microbiome interactions, opening new paths for side effect control and drug repurposing, and broadening our view of antibiotic resistance.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Farmacorresistência Bacteriana / Avaliação Pré-Clínica de Medicamentos / Microbioma Gastrointestinal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nature Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Farmacorresistência Bacteriana / Avaliação Pré-Clínica de Medicamentos / Microbioma Gastrointestinal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Nature Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha