Molecular dissection of the evolution of carbapenem-resistant multilocus sequence type 258 <i>Klebsiella pneumoniae</i>

2014 Proceedings of the National Academy of Sciences 320 citations

Abstract

Significance Carbapenem-resistant Klebsiella pneumoniae has emerged globally as a multidrug-resistant hospital pathogen for which there are few treatment options. Clinical isolates classified by multilocus sequence typing (ST) as ST258 are the most widespread. The basis for the success of ST258 organisms above and beyond antibiotic resistance is not known, nor is it clear whether infections are caused by a single clone. We used genome sequencing to reveal unexpected genetic diversity among ST258 organisms (thus disproving the single-clone hypothesis) and identified a recombination hotspot that accounts for the majority of divergence—and presumably for serologic variation—among ST258 clinical isolates. Our findings will facilitate the development of new clinical strategies designed to prevent or treat infections caused by multidrug-resistant K. pneumoniae .

Keywords

Klebsiella pneumoniaeMultilocus sequence typingBiologyclone (Java method)Antibiotic resistanceMicrobiologyMultiple drug resistanceWhole genome sequencingDrug resistanceGenomeGeneticsGeneAntibioticsGenotypeEscherichia coli

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Year
2014
Type
article
Volume
111
Issue
13
Pages
4988-4993
Citations
320
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Frank R. DeLeo, Liang Chen, Stephen F. Porcella et al. (2014). Molecular dissection of the evolution of carbapenem-resistant multilocus sequence type 258 <i>Klebsiella pneumoniae</i>. Proceedings of the National Academy of Sciences , 111 (13) , 4988-4993. https://doi.org/10.1073/pnas.1321364111

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DOI
10.1073/pnas.1321364111