克雷伯氏菌和不动杆菌碳青霉烯酶3种表型方法及PCR快速检测方法的比较

Omnia Taher
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引用次数: 1

摘要

PCR检测碳青霉烯酶编码基因阳性,以blaOXA-48基因为主。显色培养基检测碳青霉烯酶产生菌的阳性率为98%(49/50),敏感性为100%,特异性为0%。48株PCR阳性菌株中,45株MHT检测碳青霉烯酶产生的敏感性为93.8%,特异性为0%。在48株PCR阳性分离株中,蓝碳水化合物试验阳性48株,检测碳青霉烯酶产生的敏感性为100%,特异性为100%。结论:蓝碳酶检测与PCR检测结果一致,敏感性100%,特异性100%,但无法检测到其他表型检测方法检测到的碳青霉烯酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Three Phenotypic Methods and PCR for Rapid Detection of Carbapenemase ‎Production in Klebsiella spp. and Acinetobacter spp.
of Acinetobacter isolates were positive for one or more genes coding for carbapenemase by PCR with predominance of blaOXA-48 gene. Chromogenic media gave positive results in 98% (49/50) of isolates with sensitivity 100% and specificity 0% for detection of carbapenemase producers. MHT gave positive results in 45 isolates out of 48 PCR positive isolates with a sensitivity of 93.8% and specificity 0% for detection of carbapenemase production. Blue carba test gave positive results in 48 isolates out of 48 PCR positive isolates with a sensitivity of 100% and specificity 100% for detection of carbapenemase production. Conclusion: Blue carba test agreed with PCR with a sensitivity of 100% and specificity 100%, However it failed to detect the carbapenemases detected by other phenotypic tests .
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