INTRODUCTION
The emergence and dissemination of sucsessful clones of A. baumannii is a serious problem for the medical community.
OBJECTIVE
To investigate clonal diversity of A.baumannii isolated from blood culture in patients with hematological malignancies.
MATERIAL AND METHODS
The study included A.baumannii isolated from blood culture in patients in 7 Russian hospitals (2003—2017). Two multiplex PCRs were performed to selectively amplify group 1 or group 2 alleles of the ompA, csuE, and blaOXA-51-like. Isolates were assigned to one of the sequence groups (G1—G14) according to allelic profiles.
RESULTS
A total of 96 A.baumannii were examined of those 77 (80.2%) were non-susceptible to meropenem and/or imipenem. Genes of acquired carbapenemases were detected in 79.2% (61/77) carbapenem non-susceptible isolates. The prevalent carbapenemase genes were blaOXA-24/40-like (45.9%) and blaOXA-23-like (45.9%), followed by blaOXA-58-like (6.6%), co-harboring blaOXA-24/40-like and blaOXA-23-like (1.6%). During the study period the rate of blaOXA-23-like-carrying A.baumannii increased from 30% (2003—2010) up to 53.7% (2011—2017), whereas A.baumannii harboring blaOXA-24/40-like decreased from 50% (2003—2010) to 43.9% (2011—2017). The majority of A.baumannii carrying acquired carbapenemase genes (62.3%) belonged to G1 group (international clone II, IC II) which is widespread in the world. G1 (IC II) isolates harboring blaOXA-23-like were not detected during 2003—2010 whereas in 2011—2017 G1 (IC II) A.baumannii carrying blaOXA-23-like accounted for 86.4%. During the study period, there was a slight decrease in the rate of blaOXA-24/40-like-carrying A.baumannii from 70% (2003—2010) to 53.7% (2011—2017).
CONCLUSIONS
The increase of G1 (ICII) A.baumannii harboring blaOXA-23-like was observed during last years (2011—2017).