Mutters N T, Zimmermann S, Kaase M, Mischnik A
Department of Infectious Diseases, Medical Microbiology and Hygiene, Heidelberg University Hospital, 69120, Heidelberg, Germany.
National Reference Laboratory for Multidrug-Resistant Gram-Negative Bacteria, Department of Medical Microbiology, Ruhr University Bochum, 44801, Bochum, Germany.
Eur J Clin Microbiol Infect Dis. 2015 Dec;34(12):2429-37. doi: 10.1007/s10096-015-2498-3. Epub 2015 Oct 3.
Treatment options for multidrug-resistant Gram-negative infections are scarce and therefore alternatives with a narrow spectrum or new agents are sought. Antimicrobial susceptibility to temocillin, mecillinam, ceftazidime, and ceftazidime/avibactam was determined using Etest and disk diffusion according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) methodology. A total of 77 carbapenem-nonsusceptible Enterobacteriaceae were studied, including Klebsiella pneumoniae (26%), Escherichia coli (26%), Enterobacter cloacae (26%), and Enterobacter aerogenes (22%). Several phenotypic tests, PCRs followed by sequencing and a microbiological bioassay excluded carbapenemase production in all isolates. Antimicrobial susceptibility rates were low for temocillin (15.6%, minimum inhibitory concentration [MIC] range 2 to >1,024 μg/ml), moderate for mecillinam (59.7%, MIC range 0.25 to >256 μg/ml), and excellent for ceftazidime/avibactam (100%, zone diameter range 19 to 32 mm, median 25 mm). 5.2% of the isolates were susceptible to ceftazidime alone (zone diameter range 6 to 32 mm). In this study, mecillinam exhibited moderate and ceftazidime/avibactam excellent in vitro antimicrobial activity against carbapenem-nonsusceptible Enterobacteriaceae without carbapenemase production. Ceftazidime/avibactam was able to restore previously reduced susceptibility to ceftazidime in all isolates, thus potentiating its activity. Temocillin only exhibited low in vitro antimicrobial activity against the isolates. Further evaluation of mecillinam and ceftazidime/avibactam with regard to the potential clinical utility against infections caused by these pathogens has to be performed.
耐多药革兰氏阴性菌感染的治疗选择匮乏,因此人们在寻找窄谱替代品或新型药物。根据欧洲抗菌药物敏感性试验委员会(EUCAST)的方法,使用Etest和纸片扩散法测定了替莫西林、美西林、头孢他啶以及头孢他啶/阿维巴坦的抗菌敏感性。共研究了77株对碳青霉烯类不敏感的肠杆菌科细菌,包括肺炎克雷伯菌(26%)、大肠埃希菌(26%)、阴沟肠杆菌(26%)和产气肠杆菌(22%)。多项表型试验、PCR测序以及微生物生物测定排除了所有分离株产生碳青霉烯酶的可能性。替莫西林的抗菌敏感率较低(15.6%,最低抑菌浓度[MIC]范围为2至>1024μg/ml),美西林为中等(59.7%,MIC范围为0.25至>256μg/ml),头孢他啶/阿维巴坦则极佳(100%,抑菌圈直径范围为19至32mm,中位数为25mm)。5.2%的分离株仅对头孢他啶敏感(抑菌圈直径范围为6至32mm)。在本研究中,美西林对不产生碳青霉烯酶的耐碳青霉烯类肠杆菌科细菌表现出中等程度的体外抗菌活性,头孢他啶/阿维巴坦则表现优异。头孢他啶/阿维巴坦能够恢复所有分离株先前降低的对头孢他啶的敏感性,从而增强其活性。替莫西林对这些分离株仅表现出较低的体外抗菌活性。必须进一步评估美西林和头孢他啶/阿维巴坦针对这些病原体引起的感染的潜在临床效用。