Nested Russian Doll-Like Genetic Mobility Drives Rapid Dissemination of the Carbapenem Resistance Gene bla KPC

Author:

Sheppard Anna E.1,Stoesser Nicole1ORCID,Wilson Daniel J.1,Sebra Robert2,Kasarskis Andrew2,Anson Luke W.1,Giess Adam1,Pankhurst Louise J.1,Vaughan Alison1,Grim Christopher J.3,Cox Heather L.4,Yeh Anthony J.4,Sifri Costi D.45,Walker A. Sarah1,Peto Tim E.1,Crook Derrick W.16,Mathers Amy J.47,

Affiliation:

1. Modernizing Medical Microbiology Consortium, Nuffield Department of Clinical Medicine, John Radcliffe Hospital, Oxford University, Oxford, United Kingdom

2. Icahn Institute and Department of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA

3. Food and Drug Administration, Laurel, Maryland, USA

4. Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia Health System, Charlottesville, Virginia, USA

5. Office of Hospital Epidemiology, University of Virginia Health System, Charlottesville, Virginia, USA

6. Public Health England, Microbiology Services, London, United Kingdom

7. Clinical Microbiology, Department of Pathology, University of Virginia Health System, Charlottesville, Virginia, USA

Abstract

ABSTRACT The recent widespread emergence of carbapenem resistance in Enterobacteriaceae is a major public health concern, as carbapenems are a therapy of last resort against this family of common bacterial pathogens. Resistance genes can mobilize via various mechanisms, including conjugation and transposition; however, the importance of this mobility in short-term evolution, such as within nosocomial outbreaks, is unknown. Using a combination of short- and long-read whole-genome sequencing of 281 bla KPC -positive Enterobacteriaceae isolates from a single hospital over 5 years, we demonstrate rapid dissemination of this carbapenem resistance gene to multiple species, strains, and plasmids. Mobility of bla KPC occurs at multiple nested genetic levels, with transmission of bla KPC strains between individuals, frequent transfer of bla KPC plasmids between strains/species, and frequent transposition of bla KPC transposon Tn 4401 between plasmids. We also identify a common insertion site for Tn 4401 within various Tn 2 -like elements, suggesting that homologous recombination between Tn 2 -like elements has enhanced the spread of Tn 4401 between different plasmid vectors. Furthermore, while short-read sequencing has known limitations for plasmid assembly, various studies have attempted to overcome this by the use of reference-based methods. We also demonstrate that, as a consequence of the genetic mobility observed in this study, plasmid structures can be extremely dynamic, and therefore these reference-based methods, as well as traditional partial typing methods, can produce very misleading conclusions. Overall, our findings demonstrate that nonclonal resistance gene dissemination can be extremely rapid, presenting significant challenges for public health surveillance and achieving effective control of antibiotic resistance.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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