@article{979a7875b43742b7882b69249acd94c4,
title = "Molecular characteristics of carbapenemase-producing Enterobacterales in the Netherlands; results of the 2014–2018 national laboratory surveillance",
abstract = "Objectives: Carbapenem resistance mediated by mobile genetic elements has emerged worldwide and has become a major public health threat. To gain insight into the molecular epidemiology of carbapenem resistance in The Netherlands, Dutch medical microbiology laboratories are requested to submit suspected carbapenemase-producing Enterobacterales (CPE) to the National Institute for Public Health and the Environment as part of a national surveillance system. Methods: Meropenem MICs and species identification were confirmed by E-test and MALDI-TOF and carbapenemase production was assessed by the Carbapenem Inactivation Method. Of all submitted CPE, one species/carbapenemase gene combination per person per year was subjected to next-generation sequencing (NGS). Results: In total, 1838 unique isolates were received between 2014 and 2018, of which 892 were unique CPE isolates with NGS data available. The predominant CPE species were Klebsiella pneumoniae (n = 388, 43%), Escherichia coli (n = 264, 30%) and Enterobacter cloacae complex (n = 116, 13%). Various carbapenemase alleles of the same carbapenemase gene resulted in different susceptibilities to meropenem and this effect varied between species. Analyses of NGS data showed variation of prevalence of carbapenemase alleles over time with blaOXA-48 being predominant (38%, 336/892), followed by blaNDM-1 (16%, 145/892). For the first time in the Netherlands, blaOXA-181, blaOXA-232 and blaVIM-4 were detected. The genetic background of K. pneumoniae and E. coli isolates was highly diverse. Conclusions: The CPE population in the Netherlands is diverse, suggesting multiple introductions. The predominant carbapenemase alleles are blaOXA-48 and blaNDM-1. There was a clear association between species, carbapenemase allele and susceptibility to meropenem.",
keywords = "Carbapenemase activity, Carbapenemase genes, CPE, NGS, Surveillance",
author = "{van der Zwaluw}, K. and S. Witteveen and L. Wielders and {van Santen}, M. and F. Landman and {de Haan}, A. and Schouls, {L. M.} and T. Bosch and {Cohen Stuart}, {J. W.T.} and Melles, {D. C.} and {van Dijk}, K. and Visser, {C. E.} and Notermans, {D. W.} and {van Ogtrop}, {M. L.} and Werdmuller, {B. F.M.} and {van Hees}, {B. C.} and Kluytmans, {J. A.J.W.} and {van den Bijllaardt}, W. and Kraan, {E. M.} and {van der Linden}, {M. P.M.} and Mattsson, {E. E.} and Sebens, {F. W.} and {de Jong}, E. and Fr{\'e}nay, {H. M.E.} and B. Maraha and {van Griethuysen}, {A. J.} and {van Asselt}, {G. J.} and A. Demeulemeester and Wintermans, {B. B.} and {van Trijp}, M. and A. Ott and E. Bathoorn and M. Lokate and Sinnige, {J. C.} and {de Brauwer}, {E. I.G.B.} and Stals, {F. S.} and W. Silvis and Bakker, {L. J.} and Dorigo-Zetsma, {J. W.} and B. Ridwan and K. Waar and Bernards, {A. T.} and {van Mens}, {S. P.} and N. Roescher and Nabuurs-Franssen, {M. H.} and H. Wertheim and T. Sch{\"u}lin and Diederen, {B. M.W.} and L. Bode and {van Rijn}, M. and {Dutch CPE Surveillance Study Group}",
note = "Publisher Copyright: {\textcopyright} 2020 National Institute for Public Health and the Environment, Bilthoven, The Netherlands",
year = "2020",
month = oct,
day = "1",
doi = "10.1016/j.cmi.2020.01.027",
language = "English",
volume = "26",
pages = "1412.e7--1412.e12",
journal = "Clinical Microbiology and Infection",
issn = "1198-743X",
publisher = "ELSEVIER SCI LTD",
number = "10",
}