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[一种针对引起泌尿系统感染的肠杆菌科细菌的新型快速抗生素敏感性检测方法的评估]

[Evaluation of a new and rapid antibiotic sensitivity method testing for Enterobacteriaceae responsible for urinary infections].

作者信息

Laudat P, Crouzier C

机构信息

Laboratoire d'Analyses Médicales Arnaud, TOURS, France.

出版信息

Pathol Biol (Paris). 1997 May;45(5):389-93.

PMID:9296090
Abstract

URIFAST Es et Es Plus (International Microbio, Signes, France) are rapid antimicrobial susceptibility testing method in broth medium without using an automatic reader. A screening assay (URIFAST Quatro 1C ou URIFAST Twin 1C) is performed with a 4 or 9 antimicrobial agents with a concentration c' below the low critical concentration (c) defined by the Comité de l'Antibiogramme de la Société Française de Microbiologie (CA-SFM). When a bacterial strain is presumed resistant, an antimicrobial susceptibility test with the two critical concentrations (CA-SFM) can be performed with 5 or 10 antimicrobial agents antibiotiques (URIFAST Twin ABG ou URIFAST ABG). 140 strains of Enterobacteriaceae from urinary tract infections; E. coli (n = 94), P. mirabilis (n = 13), K. pneumoniae (n = 4), K. oxytoca (n = 6), C. diversus (n = 3), P. vulgaris (n = 1), M. morganii (n = 3), C. freundii (n = 4), E. aerogenes (n = 2), E. cloacae (n = 5) and S. marcescens (n = 5); were isolated with CPS ID2 (bioMérieux, Marcy l'Etoile, France). URIFAST results were compared to Rapid ATB Ur et ATB Ur results obtained after reading with ATB expression (bioMerieux). For each discrepancy, the minimal inhibitory concentration (MIC) by agar dilution was used as the reference method. Agreement obtained were 98.57% with Quatro 1C, 98.40% with Twin 1C, 98.14% with Twin ABG and 98.39% with ABG. 94% of beta-lactams susceptible Enterobacteriaceae were detected by the screening tray with the antimicrobial agent concentration c'. URIFAST Es et Es Plus are standardized and easy-to-use methods. Because of their good performances, the URIFAST methods can be used to test antimicrobial susceptibility for Enterobacteriaceae from urinary tract infections.

摘要

URIFAST Es和Es Plus(法国国际微生物公司Signes)是无需使用自动读数仪的肉汤培养基快速抗菌药敏试验方法。采用4种或9种抗菌药物进行筛选试验(URIFAST Quatro 1C或URIFAST Twin 1C),其浓度c'低于法国微生物学会抗菌谱委员会(CA-SFM)定义的低临界浓度(c)。当推测某一细菌菌株耐药时,可使用5种或10种抗菌药物(URIFAST Twin ABG或URIFAST ABG)进行两种临界浓度(CA-SFM)的抗菌药敏试验。从尿路感染中分离出140株肠杆菌科细菌;大肠杆菌(n = 94)、奇异变形杆菌(n = 13)、肺炎克雷伯菌(n = 4)、产酸克雷伯菌(n = 6)、多变克雷伯菌(n = 3)、普通变形杆菌(n = 1)、摩根摩根菌(n = 3)、弗氏柠檬酸杆菌(n = 4)、产气肠杆菌(n = 2)、阴沟肠杆菌(n = 5)和粘质沙雷氏菌(n = 5);使用CPS ID2(法国生物梅里埃公司,马尔西-埃图瓦勒)分离得到。将URIFAST结果与用ATB Expression(生物梅里埃公司)读数后获得的Rapid ATB Ur和ATB Ur结果进行比较。对于每一处差异,采用琼脂稀释法测定的最低抑菌浓度(MIC)作为参考方法。Quatro 1C的符合率为98.57%,Twin 1C为98.40%,Twin ABG为98.14%,ABG为98.39%。94%对β-内酰胺敏感的肠杆菌科细菌可通过含抗菌药物浓度c'的筛选板检测出来。URIFAST Es和Es Plus是标准化且易于使用的方法。由于其良好的性能,URIFAST方法可用于检测尿路感染中肠杆菌科细菌的抗菌药敏情况。

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