Functional metagenomic libraries generated from anthropogenically impacted environments reveal importance of metabolic genes in biocide and antibiotic resistance (article)
dc.contributor.author | Murray, AK | |
dc.contributor.author | Zhang, L | |
dc.contributor.author | Snape, J | |
dc.contributor.author | Gaze, WH | |
dc.date.accessioned | 2023-03-03T11:38:13Z | |
dc.date.issued | 2023-02-26 | |
dc.date.updated | 2023-03-03T10:55:32Z | |
dc.description.abstract | Anthropogenic activities result in the release of antimicrobial resistant bacteria and a cocktail of antimicrobial compounds into the environment that may directly select or indirectly co-select for antimicrobial resistance (AMR). Many studies use metagenome sequencing or qPCR-based approaches to study the environmental resistome but these methods are limited by a priori knowledge. In this study, a functional metagenomic approach was used to explore biocide resistance mechanisms in two contaminated environments and a pristine site, and to identify whether potentially novel genes conferring biocide resistance also conferred resistance or reduced susceptibility to antibiotics. Resistance was predominately mediated through novel mechanisms exclusive of the well-known qac efflux genes. UDP-galactose 4-epimerase (galE) –like genes were identified in both contaminated environments and were shown to confer cross-resistance to biocides and clinically important antibiotics for the first time (to our knowledge), compared to knockout mutants. GalE -like genes were also co-located with transposons, suggesting mobilisation potential. These results show that housekeeping genes may play a significant yet underappreciated role in AMR in environmental microbiomes. | en_GB |
dc.description.sponsorship | Biotechnology & Biological Sciences Research Council (BBSRC) | en_GB |
dc.description.sponsorship | Natural Environment Research Council (NERC) | en_GB |
dc.format.extent | 100184- | |
dc.identifier.citation | Vol 4, article 100184 | en_GB |
dc.identifier.doi | https://doi.org/10.1016/j.crmicr.2023.100184 | |
dc.identifier.grantnumber | BB/L502509/1 | en_GB |
dc.identifier.grantnumber | NE/M01133X/1 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/132598 | |
dc.identifier | ORCID: 0000-0002-1388-754X (Murray, Aimee K) | |
dc.identifier | ORCID: 0000-0002-9345-6204 (Gaze, William H) | |
dc.language.iso | en | en_GB |
dc.publisher | Elsevier | en_GB |
dc.relation.url | https://doi.org/10.24378/exe.4524 | en_GB |
dc.rights | © 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). | en_GB |
dc.subject | Antimicrobial resistance | en_GB |
dc.subject | Biocide | en_GB |
dc.subject | Functional metagenomics | en_GB |
dc.title | Functional metagenomic libraries generated from anthropogenically impacted environments reveal importance of metabolic genes in biocide and antibiotic resistance (article) | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2023-03-03T11:38:13Z | |
dc.identifier.issn | 2666-5174 | |
exeter.article-number | 100184 | |
dc.description | This is the final version. Available from Elsevier via the DOI in this record. | en_GB |
dc.description | The research data supporting this publication are provided within this paper and the supplementary information accompanying this publication. The sequence data are openly available from the University of Exeter's institutional repository Open Research Exeter (ORE) at https://doi.org/10.24378/exe.4524. | en_GB |
dc.identifier.journal | Current Research in Microbial Sciences | en_GB |
dc.relation.ispartof | Current Research in Microbial Sciences | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_GB |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2023-02-26 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2023-03-03T11:30:02Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2023-03-03T11:38:18Z | |
refterms.panel | A | en_GB |
Files in this item
This item appears in the following Collection(s)
Except where otherwise noted, this item's licence is described as © 2023 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).