Carbapenem-Resistant Klebsiella pneumoniae Strains: Susceptibility to Novel Antibiotics and Molecular Detection of the Resistance Mechanisms - A Study from Two Greek Tertiary Teaching Hospitals

M. Chatzidimitriou, P. Chatzivasileiou, G. Sakellariou, Kyriazidi Ma, D. Chatzidimitriou, F. Chatzopoulou, D Rousis, E Katsifa, E. Vagdatli, Lialiaris Th
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引用次数: 1

Abstract

Objectives: We 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. Materials and methods: Forty-seven carbapenem resistant K. pneumoniae strains were collected in G. Papanikolaou and Ippokrateio hospital of Thessaloniki from 1/11/2016 to 5/1/2018 and 26/1/2017 to 19/4/2017 respectively. Strain identification and antimicrobial susceptibility was conducted by Vitek 2 system (Biomerieux France). Susceptibility against new antimicrobial agents was examined by disk diffusion method. Polymerase chain reaction (PCR) was used for the detection of blaKPC, blaVIM, blaNDM and blaOXA-48 genes. Results: The EDTA-boronic acid disk synergy test performed on the 24 K. pneumoniae strains from G. Papanikolaou hospital demonstrated that 8 (33.3%) yielded positive for metallo-b-lactamases (MBL) and 16 (66.6%) for K. pneumoniae carbapenemases (KPC) production. Gentamycin demonstrated the highest in vitro activity (82.6%) among the 23 K. pneumoniae strains from Ippokrateio hospital followed by colistin (73.9%) and tigecycline (69.5%). All strains from G. Papanikolaou hospital were sensitive to colistin whereas the 70.8% of them displayed susceptibility to gentamycin. Ceftazidime/ avibactam showed the highest sensitivity (76.6%) in all strains followed by eravacyclin (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. Conclusions: Well established antimicrobial agents such as colistin, gentamycin and tigecycline and novel antibiotics like ceftazidime/avibactam and eravacycline may be reliable options for the treatment of invasive infections caused by KPC-producing pathogens.
耐碳青霉烯肺炎克雷伯菌对新型抗生素的敏感性及耐药机制的分子检测——来自希腊两所三级教学医院的研究
目的:评价希腊两所三级教学医院分离的肺炎克雷伯菌对碳青霉烯类药物的耐药机制及其对常用和新型抗菌药物的敏感性。材料与方法:分别于2016年11月1日至2018年5月1日和2017年1月26日至2017年4月19日在塞萨洛尼基市G. Papanikolaou医院和ipokrateio医院采集了47株耐碳青霉烯类肺炎克雷伯菌。采用Vitek 2系统(Biomerieux France)进行菌株鉴定和药敏试验。采用纸片扩散法检测对新型抗菌药物的药敏。采用聚合酶链反应(PCR)检测blaKPC、blaVIM、blaNDM和blaxa -48基因。结果:对帕帕尼克劳医院24株肺炎克雷伯菌进行edta -硼酸盘协同试验,8株(33.3%)产生金属-b-内酰胺酶(MBL), 16株(66.6%)产生碳青霉烯酶(KPC)。体外活性最高的是庆大霉素(82.6%),其次是粘菌素(73.9%)和替加环素(69.5%)。所有来自G. Papanikolaou医院的菌株均对粘菌素敏感,其中对庆大霉素敏感的占70.8%。所有菌株对头孢他啶/阿维巴坦的敏感性最高(76.6%),其次是依拉瓦环素(66.6%)。blaKPC基因检出30株(63.8%),blaNDM基因检出11株(23.4%),blaVIM基因检出6株(12.8%)。未检测到blaOXA-48基因。结论:成熟的抗菌药物如粘菌素、庆大霉素和替加环素以及新型抗生素如头孢他啶/阿维巴坦和依瓦环素可能是治疗kpc产生病原体引起的侵袭性感染的可靠选择。
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