[Clinical assessment of novel ChromID ESBL agar plates for detection of ESBL producers in the family Enterobacteriaceae].

Eriko Kasuga, Takehisa Matsumoto, Eiko Hidaka, Harumi Oguchi, Shinichiro Kanai, Kozue Oana, Kazuyoshi Yamauchi, Takayuki Honda, Yoshiyuki Kawakami
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Abstract

Extended-Spectrum beta-Lactamase (ESBL)-producers in the family Enterobacteriaceae are recognized worldwide as nosocomial pathogens, however it is difficult to screen them in the routine laboratory processing. ChromID ESBL agar newly developed for screening ESBL-producing Enterobacteriaceae was released in Japan in April, 2007. We evaluated the clinical assessment of ChromID ESBL agar in routine microbiology laboratory. The 47 strains investigated were clinical isolates belonging to the family Enterobacteriaceae with the MICs of cefpodoxime greater than 2 mug/ml. The 27 ESBL-producers examined were comprising of 19 Escherichia coli, 3 Klebsiella oxytoca, 1 Citrobacter freundii, 3 Enterobacter cloacae, and 1 S. marcescens (ESBL group) and 20 ESBL non-producers consiating of 5 K. oxytoca, 1 Proteus mirabilis, 1 P. vlugaris, 2 Serratia marcescens, 8 C. freundii, 2 Enterobacter cloacae, and 1 E. aerogenes (non-ESBL group). Characterization of beta-lactamase genes was carried out by use of polymerase chain reaction. As the results, the sensitivity and the specificity of ChromID ESBL agar plates after incubation for 18 hours was 100% and 20%, respectively. It should be noted that the values of specificity was extremely low compared with those of the sensitivity. These findings clearly suggested that in cases of utilizing ChromID ESBL agar plates, it should be important to consider its characteristic properties, as even the ESBL-non-producers could grow on these media only when they were resistant to CPDX.

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[新型ChromID ESBL琼脂板检测肠杆菌科ESBL产生菌的临床评价]。
肠杆菌科的广谱β -内酰胺酶(ESBL)产生菌是世界范围内公认的医院病原菌,但在常规实验室处理中难以筛选。用于筛选产ESBL肠杆菌科细菌的新开发的ChromID ESBL琼脂于2007年4月在日本发布。我们在常规微生物实验室评估了ChromID ESBL琼脂的临床评价。47株临床分离菌株均属肠杆菌科,头孢多肟的mic值大于2 mug/ml。27株ESBL产生菌包括19株大肠埃希菌、3株氧化克雷伯菌、1株弗氏柠檬酸杆菌、3株阴沟肠杆菌和1株粘质葡萄球菌(ESBL组);20株ESBL非产生菌包括5株氧化克雷伯菌、1株奇异变形杆菌、1株普通假单胞菌、2株粘质沙雷菌、8株弗氏杆菌、2株阴沟肠杆菌和1株产气埃希菌(非ESBL组)。利用聚合酶链反应对β -内酰胺酶基因进行鉴定。结果表明,培养18小时后,ChromID ESBL琼脂板的敏感性为100%,特异性为20%。值得注意的是,特异性值与敏感性值相比非常低。这些发现清楚地表明,在使用ChromID ESBL琼脂板的情况下,考虑其特性应该是重要的,因为即使是非ESBL生产者也只有当它们对CPDX具有抗性时才能在这些培养基上生长。
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