Abstract
The worldwide spread of Klebsiella pneumoniae carbapenemase-producing Klebsiella pneumoniae (KPCKp) isolates was reported to be caused by dissemination of 1 clonal complex (i.e., clonal group [CG] 258, which includes sequence types [STs] 258 and 512). We conducted whole-genome sequencing and epidemiologic analysis of all KPC-Kp isolates in France in 2018 and found that new successful high-risk clones of ST147, ST307, ST231, and ST383 are now the main drivers of blaKPC genes. The blaKPC genes were mostly carried by Tn4401a and Tn4401d structures and a new non-Tn4401 element. Our epidemiologic investigations showed that the emergence of these non-CG258 KPC-Kp isolates in France was linked to dissemination of these clones from Portugal. Thus, KPC-Kp epidemiology has changed in Europe, at least in several non-KPC-endemic countries of western Europe, such as France and Portugal, where CG258 is not the most prevalent clone.
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CITATION STYLE
Bonnin, R. A., Jousset, A. B., Chiarelli, A., Emeraud, C., Glaser, P., Naas, T., & Dortet, L. (2020). Emergence of new non-clonal group 258 high-risk clones among Klebsiella pneumoniae Carbapenemase-Producing K. Pneumoniae Isolates, France. Emerging Infectious Diseases, 26(6), 1212–1220. https://doi.org/10.3201/EID2606.191517
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