Institute for Infectious Diseases (IFIK), University of Bern, Friedbühlstrasse 51, CH-3001, Bern, Switzerland.
Graduate School of Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
Eur J Clin Microbiol Infect Dis. 2022 Jul;41(7):1087-1091. doi: 10.1007/s10096-022-04462-z. Epub 2022 May 28.
Only two plasmid-mediated carbapenemases (KPC-2 and VIM-1) are reported in Klebsiella grimontii. Here, we report two bla-positive isolates that were identified as K. oxytoca and E. coli by MALDI-TOF MS in the same rectal swab. Whole-genome sequencing indicated that K. oxytoca was actually K. grimontii of ST391, whereas E. coli was of ST10. In both, bla was carried by a pQil conjugative plasmid. The core-genome analysis identified additional bla-positive K. grimontii strains from public databases, most of which were misidentified as K. oxytoca. Since K. grimontii represents an emerging reservoir of resistance traits, routine tools should improve their ability to detect this species.
仅报道了两种质粒介导的碳青霉烯酶(KPC-2 和 VIM-1)在克氏肺炎克雷伯菌中。在此,我们报告了两株 bla 阳性分离株,这两株分离株在同一个直肠拭子中通过 MALDI-TOF MS 鉴定为产酸克雷伯菌和大肠埃希菌。全基因组测序表明,产酸克雷伯菌实际上是 ST391 型的克氏肺炎克雷伯菌,而大肠埃希菌则是 ST10 型。在这两种情况下,bla 均由一个 pQil 可接合质粒携带。核心基因组分析从公共数据库中鉴定出了其他 bla 阳性克氏肺炎克雷伯菌株,其中大多数被错误鉴定为产酸克雷伯菌。由于克氏肺炎克雷伯菌代表了一种新兴的耐药基因库,常规工具应该提高它们检测该物种的能力。