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Role of mobile genetic elements in the global dissemination of the carbapenem resistance gene bla NDM .

Mislav AcmanRuobing WangLucy van DorpLiam P ShawQi WangNina LuhmannYuyao YinShijun SunHongbin ChenHui WangFrancois Balloux
Published in: Nature communications (2022)
The mobile resistance gene bla NDM encodes the NDM enzyme which hydrolyses carbapenems, a class of antibiotics used to treat some of the most severe bacterial infections. The bla NDM gene is globally distributed across a variety of Gram-negative bacteria on multiple plasmids, typically located within highly recombining and transposon-rich genomic regions, which leads to the dynamics underlying the global dissemination of bla NDM to remain poorly resolved. Here, we compile a dataset of over 6000 bacterial genomes harbouring the bla NDM gene, including 104 newly generated PacBio hybrid assemblies from clinical and livestock-associated isolates across China. We develop a computational approach to track structural variants surrounding bla NDM , which allows us to identify prevalent genomic contexts, mobile genetic elements, and likely events in the gene's global spread. We estimate that bla NDM emerged on a Tn125 transposon before 1985, but only reached global prevalence around a decade after its first recorded observation in 2005. The Tn125 transposon seems to have played an important role in early plasmid-mediated jumps of bla NDM , but was overtaken in recent years by other elements including IS26-flanked pseudo-composite transposons and Tn3000. We found a strong association between bla NDM -carrying plasmid backbones and the sampling location of isolates. This observation suggests that the global dissemination of the bla NDM gene was primarily driven by successive between-plasmid transposon jumps, with far more restricted subsequent plasmid exchange, possibly due to adaptation of plasmids to their specific bacterial hosts.
Keyphrases
  • klebsiella pneumoniae
  • escherichia coli
  • copy number
  • multidrug resistant
  • genome wide
  • crispr cas
  • gram negative
  • dna methylation
  • early onset
  • pseudomonas aeruginosa