Patel Bhargav, Patel Kinjal, Shetty Anjali, Soman Rajeev, Rodrigues Camilla
Consultant Microbiologist, HCG Hospital, Ahmedabad, Gujarat.
Clinical Assistant.
J Assoc Physicians India. 2017 Sep;65(9):14-16.
Antibiotic treatment of Urinary Tract Infections (UTI) is becoming increasingly difficult due to emergence of multi-drug resistant (ESBLs, AmpC, CRE) uropathogens. Fosfomycin is an old antibiotic that has evoked renewed interest with unique properties of not sharing any structural similarity and lack of cross-resistance with other antimicrobial agents. Our aim is to evaluate in-vitro activity of Fosfomycin against urinary tract Enterobacteriaceae.
MATERIAL & METHODS: The study period was March 2014 to September 2015. All 72 isolates were identified using conventional biochemical tests. Antimicrobial susceptibility testing was performed using the automated broth microdilution system Vitek 2 (bio- Mérieux, Inc., Durham, NC). Fosfomycin susceptibility was determined by the E-test (bioMérieux, Inc., Durham, NC) method. Interpretive criteria from the Clinical and Laboratory Standards Institute (CLSI) for fosfomycin susceptibility are not available for the Enterobacteriaceae other than Escherichia coli. Therefore, results were interpreted according to criteria for E. coli (i.e., susceptible at a MIC of ≤ 64 μg/ml), as has been reported previously.
Overall, 79.16% (57/72) isolates were susceptible to fosfomycin w i t h 92.00% (23/25) susceptibility in ESBL producing enterobacteriaceae and 72.34% (34/47) in CRE. One CRE isolate has developed resistant while on treatment. There was not much difference in number of susceptible isolates CLSI:EUCAST = 57:53,but number of resistant isolates was more with EUCAST (CLSI:EUCAST = 10:19).
Study demonstrate that, a considerable proportion (79.16%) of the multidrug-resistant Enterobacteriaceae with diverse resistance mechanisms, including ESBL and CRE, found susceptible to fosfomycin. Consequently, fosfomycin may currently be considered a useful antibiotic agent in the treatment armamentarium of UTIs.
由于多重耐药性尿路病原体(超广谱β-内酰胺酶、AmpC、耐碳青霉烯类肠杆菌科细菌)的出现,尿路感染(UTI)的抗生素治疗正变得越来越困难。磷霉素是一种古老的抗生素,因其具有独特的性质,即与其他抗菌剂没有任何结构相似性且不存在交叉耐药性,从而重新引起了人们的关注。我们的目的是评估磷霉素对尿路肠杆菌科细菌的体外活性。
研究时间为2014年3月至2015年9月。所有72株分离菌均采用传统生化试验进行鉴定。使用自动肉汤微量稀释系统Vitek 2(生物梅里埃公司,北卡罗来纳州达勒姆)进行药敏试验。磷霉素敏感性通过E试验(生物梅里埃公司,北卡罗来纳州达勒姆)方法测定。除大肠杆菌外,临床和实验室标准协会(CLSI)针对肠杆菌科细菌的磷霉素敏感性解释标准尚无可用标准。因此,结果按照大肠杆菌的标准进行解释(即,最低抑菌浓度≤64μg/ml时为敏感),如先前报道。
总体而言,79.16%(57/72)的分离菌对磷霉素敏感,产超广谱β-内酰胺酶肠杆菌科细菌的敏感性为92.00%(23/25),耐碳青霉烯类肠杆菌科细菌的敏感性为72.34%(34/47)。1株耐碳青霉烯类肠杆菌科细菌分离菌在治疗期间出现耐药。敏感分离菌数量在CLSI标准与欧洲药敏试验委员会(EUCAST)标准之间差异不大(CLSI:EUCAST = 57:53),但EUCAST标准下的耐药分离菌数量更多(CLSI:EUCAST = 10:19)。
研究表明,相当一部分(79.16%)具有多种耐药机制(包括超广谱β-内酰胺酶和耐碳青霉烯类肠杆菌科细菌)的多重耐药肠杆菌科细菌对磷霉素敏感。因此,目前磷霉素可被视为尿路感染治疗药物库中的一种有用抗生素。