1School of Biomedical Sciences, International Hellenic University, Thessaloniki, Greece.
2Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Acta Microbiol Immunol Hung. 2021 Jan 29;68(2):65-72. doi: 10.1556/030.2021.01364. Print 2021 Jun 21.
The present study evaluated the carbapenem resistance mechanisms of Klebsiella pneumoniae strains isolated in two Greek tertiary teaching hospitals and their susceptibility to currently used and novel antimicrobial agents.Forty-seven carbapenem resistant K. pneumoniae strains were collected in G. Papanikolaou and Ippokrateio hospital of Thessaloniki between 2016 and 2018. Strain identification and antimicrobial susceptibility was conducted by Vitek 2 system (Biomérieux France). Susceptibility against new antimicrobial agents was examined by disk diffusion method. Polymerase chain reaction (PCR) was used to detect blaKPC, blaVIM, blaNDM and blaOXA-48 genes.The meropenem-EDTA and meropenem-boronic acid synergy test performed on the 24 K. pneumoniae strains demonstrated that 8 (33.3%) yielded positive for metallo-beta-lactamases (MBL) and 16 (66.6%) for K. pneumonia carbapenemases (KPC) production. Colistin demonstrated the highest in vitro activity (87.7%) among the 47 K. pneumoniae strains followed by gentamicin (76.5%) and tigecycline (51%). Among new antibiotics ceftazidime/avibactam showed the highest sensitivity (76.6%) in all strains followed by eravacycline (66.6%). The blaKPC gene was present in 30 strains (63.8%), the blaNDM in 11 (23.4%) and the blaVIM in 6 (12.8%). The blaOXA-48 gene was not detected.Well established antimicrobial agents such as colistin, gentamicin and tigecycline and novel antibiotics like ceftazidime/avibactam and eravacycline can be reliable options for the treatment of invasive infections caused by carbapenem-resistant K. pneumoniae.
本研究评估了在希腊两家三级教学医院分离的肺炎克雷伯菌菌株的碳青霉烯类耐药机制及其对目前使用和新型抗菌药物的敏感性。2016 年至 2018 年,在塞萨洛尼基的 G. Papanikolaou 和 Ippokrateio 医院收集了 47 株耐碳青霉烯类肺炎克雷伯菌。通过 Vitek 2 系统(法国生物梅里埃)进行菌株鉴定和抗菌药物敏感性检测。通过纸片扩散法检测对新型抗菌药物的敏感性。聚合酶链反应(PCR)用于检测 blaKPC、blaVIM、blaNDM 和 blaOXA-48 基因。对 24 株肺炎克雷伯菌进行的美罗培南-EDTA 和美罗培南-硼酸协同试验显示,8 株(33.3%)产金属β-内酰胺酶(MBL)阳性,16 株(66.6%)产肺炎克雷伯菌碳青霉烯酶(KPC)。47 株肺炎克雷伯菌中,多黏菌素的体外活性最高(87.7%),其次是庆大霉素(76.5%)和替加环素(51%)。新型抗生素中,头孢他啶/阿维巴坦在所有菌株中的敏感性最高(76.6%),其次是依拉环素(66.6%)。blaKPC 基因存在于 30 株(63.8%),blaNDM 存在于 11 株(23.4%),blaVIM 存在于 6 株(12.8%)。blaOXA-48 基因未检出。多黏菌素、庆大霉素和替加环素等已确立的抗菌药物以及头孢他啶/阿维巴坦和依拉环素等新型抗生素可作为治疗耐碳青霉烯类肺炎克雷伯菌引起的侵袭性感染的可靠选择。