The first nationwide multicenter study of Acinetobacter baumannii recovered in Serbia: emergence of OXA-72, OXA-23 and NDM-1-producing isolates

Background The worldwide emergence and clonal spread of carbapenem-resistant Acinetobacter baumannii (CRAB) is of great concern. The aim of this nationwide study was to investigate the prevalence of CRAB isolates in Serbia and to characterize underlying resistance mechanisms and their genetic relate...

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Veröffentlicht in:Antimicrobial resistance & infection control 2020-07, Vol.9 (1), p.1-101, Article 101
Hauptverfasser: Lukovic, Bojana, Gajic, Ina, Dimkic, Ivica, Kekic, Dusan, Zornic, Sanja, Pozder, Tatjana, Radisavljevic, Svetlana, Opavski, Nataša, Kojic, Milan, Ranin, Lazar
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Sprache:eng
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Zusammenfassung:Background The worldwide emergence and clonal spread of carbapenem-resistant Acinetobacter baumannii (CRAB) is of great concern. The aim of this nationwide study was to investigate the prevalence of CRAB isolates in Serbia and to characterize underlying resistance mechanisms and their genetic relatedness. Methods Non-redundant clinical samples obtained from hospitalized patients throughout Serbia were included in the prospective, observational, multicenter study conducted from January to June 2018. Samples were initially screened for the presence of Acinetobacter baumannii-calcoaceticus (Acb) complex using conventional bacteriological techniques. Acb complexes recovered from clinical samples obtained from inpatients with confirmed bacterial infections were further evaluated for the presence of A. baumannii. Identification to the species level was done by the detection of the bla.sub.OXA-51 gene and rpoB gene sequence analysis. Susceptibility testing was done by disk diffusion and broth microdilution method. CRAB isolates were tested for the presence of acquired carbapenemases (bla.sub.OXA-24-like, bla.sub.OXA-23-like,bla.sub.OXA-58-like, bla.sub.OXA-143-like, bla.sub.IMP, bla.sub.VIM, bla.sub.GIM, bla.sub.SPM, bla.sub.SIM, bla.sub.NDM) by PCR. Clonal relatedness was assessed by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). Results Acb complex was isolated in 280 out of 2401 clinical samples (11.6%). Overall, A. baumannii was identified in 237 out of 280 Acb complex (84.6%). CRAB prevalence was found to be 93.7% (237/222). The MIC.sub.50/MIC.sub.90 for imipenem and meropenem were 8/> 32 [mu]g/mL and 16/> 32 [mu]g/mL, respectively. Although susceptibility was high for colistin (95.7%; n = 227) and tigecycline (75.1%; n = 178), ten isolates (4.3%) were classified as pandrug-resistant. The following carbapenemases-encoding genes were found: 98 (44.2%) bla.sub.OXA-24-like, 76 (34.5%) bla.sub.OXA-23-like, and 7 (3.2%) bla.sub.NDM-1. PFGE analysis revealed six different clusters. MLST analysis identified three STs: ST2 (n = 13), ST492 (n = 14), and ST636 (n = 10). Obtained results evaluated that circulating CRAB clones in Serbia were as follows: bla.sub.OXA66/bla.sub.OXA23/ST2 (32.4%), bla.sub.OXA66/bla.sub.OXA23/bla.sub.OXA72/ST2 (2.7%), bla.sub.OXA66/bla.sub.OXA72/ST492 (37.8%), and bla.sub.OXA66/bla.sub.OXA72/ST636 (27.1%). Conclusion This study revealed extremely high proportions of carbapenem resistance among A. baumannii cli
ISSN:2047-2994
2047-2994
DOI:10.1186/s13756-020-00769-8