快速鉴定革兰氏阴性非发酵细菌的微法。

Health laboratory science Pub Date : 1978-01-01
J B Gibson, S L Crull, K A Borchardt
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引用次数: 0

摘要

由于革兰氏阴性,非发酵细菌作为病原的当代意义,一个简单,快速的测定系统是必不可少的。因此,一种准确的、可重复的、廉价的鉴别这些生物的显微方法已经被开发出来。这套系统包括25项生化测试。碳水化合物的利用是通过对Otto和Pickett的氧化攻击和碳源同化公式的修改来证明的,而其他底物是对市售产品的修改。接种是一个双重程序,进入一个塑料多室托盘,每个孔含有100微升的基质。初始接种每孔产生10(5)个菌落形成单位。碳水化合物补充额外的50微升1 × 10(11)生物盐水悬浮液。在35℃下最长孵育48小时后读取反应。使用疾病控制中心建议的常规培养基方案和微法系统鉴定124株非发酵细菌获得的结果表明,这种快速和经济的微技术可实现高重复性和相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Micromethod for rapid identification of gram-negative, nonfermentative bacteria.

Because of the contemporary significance of gram-negative, nonfermentative bacteria as etiological agents, a simple, rapid determinative system is essential. Therefore, an accurate, reproducible, and an inexpensive micromethod for the identification of these organisms has been developed. Included in this system are twenty-five biochemical tests. Carbohydrate utilization is demonstrated by modification of Otto and Pickett's formula for oxidative attack and assimilation of carbon sources, while the other substrates are modifications of commercially available products. Inoculation is a two-fold procedure into a plastic multicompartmented tray with wells containing 100 micro liters of each substrate. Initial inoculation yields 10(5) colony forming units per well. The carbohydrates are supplemented with an additional 50 micro liters of a 1 X 10(11) saline suspension of organisms. Reactions are read after a maximum incubation of 48 hr at 35 C. The results obtained with the identification of 124 strains of nonfermentative bacteria utilizing a conventional media schema as suggested by the Center for Disease Control and the micromethod system demonstrated the high reproducibility and correlation achievable with this rapid and economical microtechnique.

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