DOES ACINETOBACTER BAUMANNII SERVES AS RESERVOIR FOR blaNDM DISSEMINATION INTO ENTEROBACTERIACEAE?

Rivka Glick 1,2 Amos Adler 1 Yehuda Carmeli 1
1Division of Epidemiology, Molecular Epidemiology and Antibiotic Resistance Laboratory, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel
2Epidemology, Tel Aviv University, Tel Aviv, Israel

Background

We aimed to describe the epidemiology and molecular features of NDM-producing Acinetobacter baumannii (NDMAb) and Enterobacteriaceae (NDME), and to explore the possibility of horizontal gene transfer (HGT) of the blaNDM between these microbial families.

Methods

The study was done at the TASMC from 12/2014 until 8/2015. Surveillance rectal cultures were tested for NDME and NDMAb. Isolates were tested by PCR for blaNDM and typing was done by PFGE. The locations of the blaNDM within the ISAba125 transposon and on a plasmid were studied by PCR`s and S1-analysis, respectively. A transmission-event (TE) was determined if patients shared the same NDME or NDMAb PFGE type and were simultaneously in the same ward. Possible HGT-related TE was considered if the two isolates shared identical blaNDM allele and transposon.

Results

The incidence of carbapenem-resistant A. baumannii-infected patients was 311, of which 15 (4.8%) were NDMAb (clinical-9, surveillance-4, both-2). The incidence of carbapenemase-producing Enterobacteriaceae-infected patients was 104, of which 13 (12.5%) were NDME (clinical-3, surveillance-8, both-2). All NDMAb isolate except one harbored blaNDM-1 that was located on an ISAba125 transposon within a plasmid. The majority of patients (n=9) were infected by one NDMAb strain. NDME were either E. coli (n=4) or K. pneumoniae (n=9) of different PFGE types. Only 1 TE of NDME was identified. All NDME isolates harbored blaNDM-1 on a transferable plasmid but the gene was located within an ISAba125 in only 3 isolates. One possible HGT-related TE from NDMAb to NDME was identified.

Conclusion

The incidences of NDMAb and NDME are similar. Whereas NDMAb appears to disseminate by clonal spread, the source of NDME remains elusive, and thus may be related to HGT from NDMAb.









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