| Literature DB >> 27284091 |
Tarah Lynch1, Liang Chen2, Gisele Peirano3, Dan B Gregson4, Deirdre L Church4, John Conly5, Barry N Kreiswirth2, Johann D Pitout6.
Abstract
During 2013, ST278 Klebsiella pneumoniae with blaNDM-7 was isolated from the urine (KpN01) and rectum (KpN02) of a patient in Calgary, Canada. The same strain (KpN04) was subsequently isolated from another patient in the same unit. Interestingly, a carbapenem-susceptible K. pneumoniae ST278 (KpN06) was obtained 1 month later from the blood of the second patient. Next-generation sequencing (NGS) revealed that the loss of carbapenem-resistance in KpN06 was due to a 5-kb deletion on the blaNDM-7-harboring IncX3 plasmid. In addition, an IncFIB plasmid in KpN06 had a 27-kb deletion that removed genes encoding for heavy metal resistance. Phylogenetic analysis showed that the K. pneumoniae ST278 from patient 2 was likely a descendant of KpN02 and that KpN06 was a close progenitor of an environmental ST278. It is unclear whether KpN06 lost the blaNDM-7 gene in vivo. This study detailed the remarkable plasticity and speed of evolutionary changes in multidrug-resistant K. pneumoniae, demonstrating the highly recombinant nature of this species. It also highlights the ability of NGS to clarify molecular microevolutionary events within antibiotic-resistant organisms.Entities:
Keywords: K. pneumoniae; ST278; blaNDM-7; carbapenemases; microevolution; plasmid
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Year: 2016 PMID: 27284091 PMCID: PMC4978375 DOI: 10.1093/infdis/jiw240
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226