dc.contributor.author |
Lynch, T.
|
|
dc.contributor.author |
Chen, L.
|
|
dc.contributor.author |
Peirano, Gisele
|
|
dc.contributor.author |
Gregson, D.B.
|
|
dc.contributor.author |
Church, D.L.
|
|
dc.contributor.author |
Conly, J.
|
|
dc.contributor.author |
Kreiswirth, B.N.
|
|
dc.contributor.author |
Pitout, Johann D.D.
|
|
dc.date.accessioned |
2016-06-24T06:20:20Z |
|
dc.date.issued |
2016-06 |
|
dc.description.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 ST278
(KpN06) was obtained one 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 ST278 K. pneumoniae from patient 2 were likely descendants 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 resistance K. pneumoniae demonstrating the highly recombinant nature of
this species. It also highlights the ability of NGS to clarify molecular micro-evolutionary events
within antibiotic-resistant organisms. |
en_ZA |
dc.description.department |
Medical Microbiology |
en_ZA |
dc.description.embargo |
2017-06-30 |
|
dc.description.librarian |
hb2016 |
en_ZA |
dc.description.sponsorship |
This work was supported in part by a research grant from the Calgary
Laboratory Services (#10009392) and grants from the National Institutes of Health (1R01AI090155 to B.N.K, and R21AI117338 to L.C). |
en_ZA |
dc.description.uri |
http://jid.oxfordjournals.org |
en_ZA |
dc.identifier.citation |
Lynch, T, Chen, L, Peirano, G, Gregson, DB, Church, DL, Conly, J, Kreiswirth, BN & Pitout, JDD 2016, 'Molecular evolution of Klebsiella pneumoniae ST278 harboring blaNDM-7 involved in nosocomial transmission', Journal of Infectious Diseases, vol. 214, no. 5, pp. 798-806. |
en_ZA |
dc.identifier.issn |
0022-1899 (print) |
|
dc.identifier.issn |
1537-6613 (online) |
|
dc.identifier.other |
10.1093/infdis/jiw240 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/53383 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
Oxford University Press |
en_ZA |
dc.rights |
© 2016 by the Infectious Diseases Society of America. All rights reserved. This is a pre-copy-editing, author-produced PDF of an article accepted for publication in Journal of Infectious Diseases following peer review. The definitive publisher-authenticated version is : Molecular evolution of Klebsiella pneumoniae ST278 harboring blaNDM-7 involved in nosocomial transmission, Journal of Infectious Diseases, vol. 214, no. 5, pp. 798-806, 2016. doi : 10.1093/infdis/jiw240, is available online at : http://jid.oxfordjournals.org. |
en_ZA |
dc.subject |
K. pneumoniae |
en_ZA |
dc.subject |
ST278 |
en_ZA |
dc.subject |
Carbapenemases |
en_ZA |
dc.subject |
blaNDM-7 |
en_ZA |
dc.subject |
Plasmid |
en_ZA |
dc.subject |
Micro-evolution |
en_ZA |
dc.title |
Molecular evolution of Klebsiella pneumoniae ST278 harboring blaNDM-7 involved in nosocomial transmission |
en_ZA |
dc.type |
Postprint Article |
en_ZA |