Operative Unit of Clinical Microbiology, S. Orsola-Malpighi University Hospital, Bologna, Italy.
Operative Unit of Clinical Microbiology, S. Orsola-Malpighi University Hospital, Bologna, Italy; University of Bologna, Italy.
Clin Microbiol Infect. 2020 Apr;26(4):516.e1-516.e4. doi: 10.1016/j.cmi.2019.11.011. Epub 2019 Nov 16.
The aim of this study was to evaluate the incidence of ceftazidime/avibactam resistance among Klebsiella pneumoniae carbapenemase (KPC)-producing K. pneumoniae (KPC-Kp) strains isolated from patients with bloodstream infection.
We collected 120 carbapenemase producing Enterobacteriaceae (CPE) strains from unique patients hospitalized in two Italian hospitals between January 2018 to February 2019. Strains were phenotypically characterized for the type of carbapenemase production and susceptibility to ceftazidime/avibactam. Ceftazidime/avibactam-resistant strains were characterized by whole-genome sequencing.
During the study period, we characterized 105 (87.5%) KPC producers among a total of 120 CPE strains. Ceftazidime/avibactam resistance was found in three KPC-Kp strains isolated from patients with no history of previous ceftazidime/avibactam-based treatment. Of note, two out of three ceftazidime-avibactam-resistant KPC-Kp were also resistant to meropenem/vaborbactam. Genomic characterization showed that a ceftazidime/avibactam-resistant KPC-Kp harboured a mixed population with D179Y mutated KPC-2, while the other two ceftazidime-avibactam-resistant KPC-Kp possessed non-functional ompK35-ompK37 and mutated ompK36 porins associated with higher copy number of bla gene.
Our results showed that incidence of ceftazidime/avibactam resistance emerged in KCP-Kp strains independently from previous antimicrobial exposure. Resistance to ceftazidime/avibactam was associated with mutations within the bla gene or porin deficiency associated with higher bla copy number and is also related to the meropenem/vaborbactam resistance.
本研究旨在评估血流感染患者中产碳青霉烯酶肺炎克雷伯菌(KPC)的肺炎克雷伯菌(KPC-Kp)分离株对头孢他啶/阿维巴坦的耐药发生率。
我们收集了 2018 年 1 月至 2019 年 2 月期间两家意大利医院住院的 120 株碳青霉烯酶肠杆菌科(CPE)菌株。对产碳青霉烯酶表型进行了鉴定,并对头孢他啶/阿维巴坦的敏感性进行了测定。采用全基因组测序对头孢他啶/阿维巴坦耐药株进行了鉴定。
在研究期间,我们从 120 株 CPE 中鉴定出 105 株(87.5%)KPC 产生者。在 3 例无头孢他啶/阿维巴坦治疗史的 KPC-Kp 患者中发现了头孢他啶/阿维巴坦耐药株。值得注意的是,3 株头孢他啶/阿维巴坦耐药的 KPC-Kp 中有 2 株对美罗培南/沃诺拉赞也耐药。基因组特征分析表明,一株头孢他啶/阿维巴坦耐药的 KPC-Kp 携带突变的 D179Y KPC-2 混合菌群,而另外两株头孢他啶/阿维巴坦耐药的 KPC-Kp 则缺乏功能的 ompK35-ompK37 和突变的 ompK36 孔蛋白,与 bla 基因的更高拷贝数有关。
我们的研究结果表明,头孢他啶/阿维巴坦耐药的发生率与 KPC-Kp 菌株的先前抗菌药物暴露无关。头孢他啶/阿维巴坦耐药与 bla 基因内的突变或孔蛋白缺失有关,与 bla 基因拷贝数增加有关,也与美罗培南/沃诺拉赞耐药有关。