Abstract
During 2013, ST278 Klebsiella pneumoniae with blaNDM-7was isolated fromthe urine (KpN01) and rectum(KpN02) of a patient inCalgary, 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 frompatient 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.
| Original language | English |
|---|---|
| Pages (from-to) | 798-806 |
| Number of pages | 9 |
| Journal | Journal of Infectious Diseases |
| Volume | 214 |
| Issue number | 5 |
| DOIs | |
| State | Published - 1 Sep 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- BlaNDM-7
- Carbapenemases
- K. pneumoniae
- Microevolution
- Plasmid
- ST278
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