| Literature DB >> 30349083 |
Albert Palleja1,2, Kristian H Mikkelsen3, Sofia K Forslund4,5,6,7,8, Alireza Kashani1,9, Kristine H Allin1,10, Trine Nielsen1, Tue H Hansen1, Suisha Liang11,12, Qiang Feng11,12, Chenchen Zhang11,12, Paul Theodor Pyl1, Luis Pedro Coelho8, Huanming Yang11,12,13, Jian Wang11,12,13, Athanasios Typas8,14, Morten F Nielsen3, Henrik Bjorn Nielsen2, Peer Bork5,8,15,16, Jun Wang17,18,19,20, Tina Vilsbøll3, Torben Hansen1,21, Filip K Knop22,23,24, Manimozhiyan Arumugam25, Oluf Pedersen26.
Abstract
To minimize the impact of antibiotics, gut microorganisms harbour and exchange antibiotics resistance genes, collectively called their resistome. Using shotgun sequencing-based metagenomics, we analysed the partial eradication and subsequent regrowth of the gut microbiota in 12 healthy men over a 6-month period following a 4-day intervention with a cocktail of 3 last-resort antibiotics: meropenem, gentamicin and vancomycin. Initial changes included blooms of enterobacteria and other pathobionts, such as Enterococcus faecalis and Fusobacterium nucleatum, and the depletion of Bifidobacterium species and butyrate producers. The gut microbiota of the subjects recovered to near-baseline composition within 1.5 months, although 9 common species, which were present in all subjects before the treatment, remained undetectable in most of the subjects after 180 days. Species that harbour β-lactam resistance genes were positively selected for during and after the intervention. Harbouring glycopeptide or aminoglycoside resistance genes increased the odds of de novo colonization, however, the former also decreased the odds of survival. Compositional changes under antibiotic intervention in vivo matched results from in vitro susceptibility tests. Despite a mild yet long-lasting imprint following antibiotics exposure, the gut microbiota of healthy young adults are resilient to a short-term broad-spectrum antibiotics intervention and their antibiotics resistance gene carriage modulates their recovery processes.Entities:
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Year: 2018 PMID: 30349083 DOI: 10.1038/s41564-018-0257-9
Source DB: PubMed Journal: Nat Microbiol ISSN: 2058-5276 Impact factor: 17.745