TY - JOUR
T1 - The plasmidome associated with Gram-negative bloodstream infections
T2 - A large-scale observational study using complete plasmid assemblies
AU - Lipworth, Samuel
AU - Matlock, Willam
AU - Shaw, Liam
AU - Vihta, Karina Doris
AU - Rodger, Gillian
AU - Chau, Kevin
AU - Barker, Leanne
AU - George, Sophie
AU - Kavanagh, James
AU - Davies, Timothy
AU - Vaughan, Alison
AU - Andersson, Monique
AU - Jeffery, Katie
AU - Oakley, Sarah
AU - Morgan, Marcus
AU - Hopkins, Susan
AU - Peto, Timothy
AU - Crook, Derrick
AU - Walker, A. Sarah
AU - Stoesser, Nicole
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Plasmids carry genes conferring antimicrobial resistance and other clinically important traits, and contribute to the rapid dissemination of such genes. Previous studies using complete plasmid assemblies, which are essential for reliable inference, have been small and/or limited to plasmids carrying antimicrobial resistance genes (ARGs). In this study, we sequenced 1,880 complete plasmids from 738 isolates from bloodstream infections in Oxfordshire, UK. The bacteria had been originally isolated in 2009 (194 isolates) and 2018 (368 isolates), plus a stratified selection from intervening years (176 isolates). We demonstrate that plasmids are largely, but not entirely, constrained to a single host species, although there is substantial overlap between species of plasmid gene-repertoire. Most ARGs are carried by a relatively small number of plasmid groups with biological features that are predictable. Plasmids carrying ARGs (including those encoding carbapenemases) share a putative ‘backbone’ of core genes with those carrying no such genes. These findings suggest that future surveillance should, in addition to tracking plasmids currently associated with clinically important genes, focus on identifying and monitoring the dissemination of high-risk plasmid groups with the potential to rapidly acquire and disseminate these genes.
AB - Plasmids carry genes conferring antimicrobial resistance and other clinically important traits, and contribute to the rapid dissemination of such genes. Previous studies using complete plasmid assemblies, which are essential for reliable inference, have been small and/or limited to plasmids carrying antimicrobial resistance genes (ARGs). In this study, we sequenced 1,880 complete plasmids from 738 isolates from bloodstream infections in Oxfordshire, UK. The bacteria had been originally isolated in 2009 (194 isolates) and 2018 (368 isolates), plus a stratified selection from intervening years (176 isolates). We demonstrate that plasmids are largely, but not entirely, constrained to a single host species, although there is substantial overlap between species of plasmid gene-repertoire. Most ARGs are carried by a relatively small number of plasmid groups with biological features that are predictable. Plasmids carrying ARGs (including those encoding carbapenemases) share a putative ‘backbone’ of core genes with those carrying no such genes. These findings suggest that future surveillance should, in addition to tracking plasmids currently associated with clinically important genes, focus on identifying and monitoring the dissemination of high-risk plasmid groups with the potential to rapidly acquire and disseminate these genes.
UR - http://www.scopus.com/inward/record.url?scp=85185621755&partnerID=8YFLogxK
U2 - 10.1038/s41467-024-45761-7
DO - 10.1038/s41467-024-45761-7
M3 - Article
C2 - 38383544
AN - SCOPUS:85185621755
SN - 2041-1723
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1612
ER -