头孢他啶-阿维巴坦对造血干细胞移植患者血液和粪便中第3代头孢菌素和碳青霉烯耐药革兰氏阴性菌的体外活性研究

Q4 Biochemistry, Genetics and Molecular Biology
D. Niyazi, T. Stoeva
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引用次数: 0

摘要

由于潜在疾病或移植本身引起的免疫抑制,造血干细胞移植(HSCT)受者容易发生侵袭性感染。胃肠道是病原体的主要来源,经常表现出多药耐药。本研究的目的是研究头孢他啶-阿维巴坦(CZA)对HSCT患者血液和粪便样本中获得的第3代头孢菌素和/或碳青霉烯耐药(CPR)革兰氏阴性菌的体外活性。共分离35株临床分离菌(肠杆菌25株,假域杆菌8株,鲍曼不动杆菌2株)。采用MALDI Biotyper (Bruker)和Phoenix系统(BD)进行鉴定和药敏感性试验。多重PCR检测β -内酰胺耐药相关基因。在研究组中,96%的肠道细菌为广谱β -乳酸酶产生菌(ESBL),且均对CZA敏感。CZA对哌拉西林-他唑巴坦耐药菌株表现出良好的活性。在CPR分离株中,91%对CZA耐药,检测到blaVIM、blaOXA-23、blaOXA-24/40、blaOXA-48基因。综上所述,CZA对产生ESBL和耐哌拉西林-他唑巴坦的革兰氏阴性菌株具有良好的活性。尽管阿维巴坦对A类酶有很强的活性,但它不能灭活B类和D类碳青霉烯酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Activity of Ceftazidime-Avibactam against 3rd Generation Cephalosporin and Carbapenem Resistant Gram-Negative Bacteria Obtained from Blood and Fecal Samples of Hematopoietic Stem Cell Transplanted Patients
The recipients of hematopoietic stem cell transplantation (HSCT) tend to develop invasive infections because of the immunosuppression caused by the underlying disease or the transplantation itself. The gastro¬intestinal tract is the major source of causative agents, often demonstrating multidrug resistance. The aim of this study is to investigate the in vitro activity of ceftazidime-avibactam (CZA) against 3rd generation ceph¬alosporin and/or carbapenem resistant (CPR) Gram-negative bacteria obtained from blood and fecal sam¬ples of patients following HSCT. Thirty-five clinical isolates were studied (Enterobacterales, n=25, Pseu-domanas spp., n=8, A. baumannii, n=2). MALDI Biotyper (Bruker) and Phoenix system (BD) were used for identification and susceptibility testing. Multiplex PCR was performed to detect genes associated with beta-lactam resistance. In the studied group 96% of the enteric bacteria were Extended Spectrum Beta Lacta¬mase producers (ESBL) and all were susceptible to CZA. CZA demonstrated an excellent activity against piperacillin-tazobactam resistant isolates. Among the CPR isolates, 91% were CZA resistant and blaVIM, blaOXA-23 and blaOXA-24/40, blaOXA-48 genes were detected. In conclusion, an excellent activity of CZA against ESBL producing and piperacillin-tazobactam resistant Gram - negative isolates was found. Despite its potent activity against class A enzymes, avibactam failed to inactivate class B and class D carbapenemases.
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来源期刊
Acta Microbiologica Bulgarica
Acta Microbiologica Bulgarica Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
0.40
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