Acquisition of genomic elements were pivotal for the success of Escherichia coli ST410

Author:

Chen Liang1,Peirano Gisele23,Kreiswirth Barry N1,Devinney Rebekah3,Pitout Johann D D234ORCID

Affiliation:

1. Hackensack Meridian Health Center for Discovery and Innovation, Hackensack Meridian School of Medicine, Nutley , NJ , USA

2. Alberta Precision Laboratories , Calgary, Alberta , Canada

3. Cummings School of Medicine, University of Calgary , #9, 3535 Research Road NW, T2L 2K8 Calgary, Alberta , Canada

4. University of Pretoria , Pretoria, Gauteng , South Africa

Abstract

Abstract Background Escherichia coli ST410 is an emerging MDR clone linked to blaCTX-M-15 and blaOXA-181. Limited comprehensive data about the global distribution of ST410 clades and mobile genetic elements associated with different β-lactamases are available. Methods Short- and long-read WGS were performed on a collection of ST410 producing carbapenemases (n = 45) obtained from 11 countries. The evolutionary history of global E. coli ST410 was also investigated. Results OXA-181 and NDM-5 were the most frequent carbapenemases and used different underlying strategies to ensure their successful association with ST410 clades. Our phylogenetic analysis of publicly available ST410 genomes amended the previously published ST410 B subclades: ST410-B1 is identical to B1/H24, ST410-B2 includes B2/H24R and B3/H24Rx, while ST410-B3 corresponds to B4/H24RxC. Long-read WGS identified the following genomic events that likely shaped the evolution of ST410-B3: (i) gyrA and parC mutations were acquired via homologous recombination events; (ii) chromosomal integration of blaCMY-2 among ST410-B3; (iii) the emergence of ST410-B3 from ST410-B2 was accompanied by the replacement of IncFII plasmids harbouring blaCTX-M-15 (i.e. F36:31:A4:B1 in ST410-B2 with F1:A1:B49 plasmids in ST410-B3); and (iv) the NDM-5 gene was integrated within F1:A1:B49 plasmids over time. Conclusions The global ST410 population producing carbapenemases is dominated by the ST410-B2 and B3 subclades with varied geographical distribution that requires ongoing genomic surveillance. We provided an updated timeline of pivotal genomic events that have shaped the success of the ST410-B3 subclade.

Funder

JPIAMR/Canadian Institute Health Research

National Institutes of Health

NIAID

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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