Abstract
Plasmids enable the dissemination of antimicrobial resistance (AMR) in common Enterobacterales pathogens, representing a major public health challenge. However, the extent of plasmid sharing and evolution between Enterobacterales causing human infections and other niches remains unclear, including the emergence of resistance plasmids. Dense, unselected sampling is essential to developing our understanding of plasmid epidemiology and designing appropriate interventions to limit the emergence and dissemination of plasmid-associated AMR. We established a geographically and temporally restricted collection of human bloodstream infection (BSI)-associated, livestock-associated (cattle, pig, poultry, and sheep faeces, farm soils) and wastewater treatment work (WwTW)-associated (influent, effluent, waterways upstream/downstream of effluent outlets) Enterobacterales. Isolates were collected between 2008 and 2020 from sites <60 km apart in Oxfordshire, UK. Pangenome analysis of plasmid clusters revealed shared 'backbones', with phylogenies suggesting an intertwined ecology where well-conserved plasmid backbones carry diverse accessory functions, including AMR genes. Many plasmid 'backbones' were seen across species and niches, raising the possibility that plasmid movement between these followed by rapid accessory gene change could be relatively common. Overall, the signature of identical plasmid sharing is likely to be a highly transient one, implying that plasmid movement might be occurring at greater rates than previously estimated, raising a challenge for future genomic One Health studies.
| Original language | English |
|---|---|
| Pages (from-to) | e85302 |
| Number of pages | 31 |
| Journal | eLife |
| Volume | 12 |
| Early online date | 7 Dec 2023 |
| DOIs | |
| Publication status | Published - 7 Dec 2023 |
Bibliographical note
Publisher Copyright:© 2023, Matlock, Lipworth et al.
Data Availability Statement
REHAB reads and assemblies and assemblies can be found in the NCBI BioProject PRJNA605147. BSI reads and assemblies can be found at https://doi.org/10.25452/figshare.plus.24573268. Analysis scripts can be found in the GitHub repository https://github.com/wtmatlock/oxfordshire-overlap (copy archived at Matlock, 2023).Funding
This work was funded by the Antimicrobial Resistance Cross-council Initiative supported by the seven research councils (grant NE/N019989/1). The UKCEH component of the REHAB consortium was supported by the Natural Environment Research Council (NERC) (grant NE/N019660/1). DWC, SG, TEAP, and NS are supported by the National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare-Associated Infections and Antimicrobial Resistance at the University of Oxford in partnership with Public Health England (PHE) (grant HPRU-2012– 10,041 and NIHR200915). DWC and TEAP are also supported by the NIHR Oxford Biomedical Research Centre. The computational aspects of this research were funded from the NIHR Oxford BRC with additional support from a Wellcome Trust Core Award Grant (grant 203141/Z/16/Z). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR, the Department of Health or Public Health England. WM and KKC are supported by a scholarship from the Medical Research Foundation National PhD Training Programme in Antimicrobial Resistance Research (MRF-145- 0004- TPG- AVISO). NS is an Oxford Martin Fellow and a Senior NIHR BRC Oxford Fellow. LPS is a Sir Henry Wellcome Postdoctoral Fellow funded by Wellcome (grant 220422/Z/20/Z). This study was funded by the Antimicrobial Resistance Cross-council Initiative supported by the seven research councils and the NIHR, UK.
Keywords
- antimicrobial resistance
- bloodstream infections
- E. coli
- Enterobacterales
- genetics
- genomic epidemiology
- genomics
- infectious disease
- K. pneumoniae
- microbiology
- One Health
- plasmid
ASJC Scopus subject areas
- General Neuroscience
- General Biochemistry,Genetics and Molecular Biology
- General Immunology and Microbiology