Phenotypic and Molecular Epidemiology of ESBL-, AmpC-, and Carbapenemase-Producing in Northern and Eastern Europe.

Front Microbiol 2019 22;10:2465. Epub 2019 Nov 22.

Department of Microbiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.

Extended-spectrum beta-lactamases (ESBL) and AmpC producing- have spread worldwide, but data about ESBL-producing- in the Northern and Eastern regions of Europe is scant. The aim of this study has been to describe the phenotypical and molecular epidemiology of different ESBL/AmpC/Carbapenemases genes in strains isolated from the Baltic States (Estonia, Latvia, and Lithuania), Norway and St. Petersburg (Russia), and to determine the predominant multilocus sequence type and single nucleotide polymorphisms diversity of isolates deduced by whole genome sequencing (WGS). A total of 10,780 clinical strains were screened for reduced sensitivity to third-generation cephalosporins. They were collected from 21 hospitals located in Estonia, Latvia, Lithuania, Norway and St. Petersburg during a 5 month period in 2012. The overall prevalence of ESBL/AmpC strains was 4.7% by phenotypical test and 3.9% by sequencing. We found more strains with the ESBL/AmpC phenotype and genotype in St. Petersburg and Latvia than other countries. Of phenotypic strains, 85% contained confirmed ESBL genes (including , , ), AmpC genes (, , , , ), or carbapenemase genes (). , and were found in all countries, but prevalence was higher in Latvia than in St. Petersburg (Russia), Estonia, Norway and Lithuania. The dominating AmpC genes were in the Baltic States and Norway, and in St. Petersburg. strains belonged to 83 different sequence types, of which the most prevalent was ST131 (40%). In conclusion, we generally found low ESBL/AmpC/Carbapenemase prevalence in strains isolated in Northern/Eastern Europe. However, several inter-country differences in distribution of particular genes and multilocus sequence types were found.

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http://dx.doi.org/10.3389/fmicb.2019.02465DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882919PMC
November 2019

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