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评估MicroScan快速阴性ID3鉴定板对肠杆菌科细菌及一些常见革兰氏阴性非发酵菌的鉴定能力。

Evaluation of the MicroScan rapid neg ID3 panel for identification of Enterobacteriaceae and some common gram-negative nonfermenters.

作者信息

O'Hara C M, Miller J M

机构信息

Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

J Clin Microbiol. 2000 Oct;38(10):3577-80. doi: 10.1128/JCM.38.10.3577-3580.2000.

Abstract

The MicroScan Rapid Neg ID3 panel (Dade Behring, Inc., West Sacramento, Calif.) is designed for the identification of gram-negative bacilli. We evaluated its ability to accurately identify Enterobacteriaceae that are routinely encountered in a clinical laboratory and glucose nonfermenting gram-negative bacilli. Using 511 stock cultures that were maintained at -70 degrees C and passaged three times before use, we inoculated panels according to the manufacturer's instructions and processed them in a Walk/Away instrument using version 22.01 software. The time to identification was 2 h and 30 min. All panel identifications were compared to reference identifications previously determined by conventional tube biochemicals. At the end of the initial 2.5-h incubation period, 405 (79.3%) identifications were correct. An additional 49 (9.6%) isolates were correctly identified after required additional off-line biochemical tests were performed. Thus, at 24 h, 88.8% of the 511 strains tested were correctly identified. Twenty-two (4.3%) were identified to the genus level only. Twenty-six (5.1%) strains were misidentified. Because the system is based on fluorogenics, there are no conventional tests readily available with which to compare possibly incorrect reactions. Of the 28 Salmonella strains that were tested, 5 were incorrectly reported. The 21 remaining errors were scattered among the genera tested. Testing on nine strains gave a result of "no identification" (very rare biotype). The Rapid Neg ID3 panel in this study approached 89% accuracy for the identification of gram-negative organisms encountered in the hospital laboratory.

摘要

MicroScan快速阴性菌ID3鉴定板(达德拜林公司,加利福尼亚州西萨克拉门托)专为革兰氏阴性杆菌的鉴定而设计。我们评估了其准确鉴定临床实验室中常见的肠杆菌科细菌和非发酵革兰氏阴性杆菌的能力。使用保存在-70℃且在使用前传代三次的511株标准菌株,我们按照制造商的说明接种鉴定板,并使用22.01版软件在Walk/Away仪器中进行处理。鉴定时间为2小时30分钟。所有鉴定板的鉴定结果均与先前通过传统试管生化方法确定的参考鉴定结果进行比较。在最初2.5小时的培养期结束时,405例(79.3%)鉴定正确。在进行所需的额外离线生化试验后,又有49例(9.6%)分离株被正确鉴定。因此,在24小时时,511株测试菌株中有88.8%被正确鉴定。22例(4.3%)仅鉴定到属水平。26例(5.1%)菌株被错误鉴定。由于该系统基于荧光技术,没有常规试验可用于比较可能错误的反应。在测试的28株沙门氏菌菌株中,有5株报告错误。其余21个错误分散在测试的各个属中。对9株菌株的测试结果为“无法鉴定”(非常罕见的生物型)。本研究中的快速阴性菌ID3鉴定板对医院实验室中遇到的革兰氏阴性菌的鉴定准确率接近89%。

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