Bale M J, McLaws S M, Fenn J P, Matsen J M
Diagn Microbiol Infect Dis. 1984 Jun;2(3):187-91. doi: 10.1016/0732-8893(84)90029-4.
The use of primary isolation plate colonial morphologic criteria (CMC) of a flat, nonmucoid, lactose-fermenting, gram-negative rod on MacConkey agar and the spot indole (SI) test from the sheep blood agar plate was evaluated as a means for identification of Escherichia coli in comparison to kit (Micro-ID, API-20E) and conventional biochemical testing. In this preliminary phase of comparison of accuracy, 427 isolates of E. coli (69.8%) from a total of 612 isolates of lactose-fermenting gram-negative rods were evaluated. Of these E. coli isolates, 357 (83.6%) fit the CMC and were SI positive; 3 (less than 1% error rate) were not E. coli. In the second phase of the evaluation, using CMC and SI alone as a means for identification of E. coli, 472 (57.6%) E. coli isolates from a total of 820 Enterobacteriaceae isolates were assessed. Of these E. coli isolates, 326 could be identified using only CMC and SI (69.1% of the E. coli isolates and 39.8% of all Enterobacteriaceae isolates); 146 (30.9%) required additional biochemical testing because of atypical colonial morphology, because of the investigator's inability to differentiate colony types on both media or lack of isolated colonies on either of the two required media, or because as isolates from sterile body sites they were processed directly to Micro-ID kits. A minimum of 40% savings on Enterobacteriaceae identification schemes without compromising accuracy was calculated. As of November 1983, a direct (labor and materials) cost savings of approximately +200.80 per 100 Enterobacteriaceae identifications was projected.
在MacConkey琼脂上使用扁平、非黏液性、乳糖发酵、革兰氏阴性杆菌的初代分离平板菌落形态学标准(CMC)以及来自羊血琼脂平板的吲哚斑点试验(SI),并与试剂盒(Micro-ID、API-20E)和传统生化检测方法相比较,以此作为鉴定大肠杆菌的手段。在这个准确性比较的初步阶段,对总共612株乳糖发酵革兰氏阴性杆菌中的427株大肠杆菌分离株(69.8%)进行了评估。在这些大肠杆菌分离株中,357株(83.6%)符合CMC且SI呈阳性;3株(错误率小于1%)不是大肠杆菌。在评估的第二阶段,仅使用CMC和SI作为鉴定大肠杆菌的手段,对总共820株肠杆菌科分离株中的472株大肠杆菌分离株(57.6%)进行了评估。在这些大肠杆菌分离株中,仅使用CMC和SI就可鉴定出326株(占大肠杆菌分离株的69.1%,占所有肠杆菌科分离株的39.8%);146株(30.9%)因菌落形态不典型、研究者无法区分两种培养基上的菌落类型、两种所需培养基上均缺乏分离菌落,或者因为它们是来自无菌身体部位的分离株而直接用Micro-ID试剂盒处理,所以需要额外的生化检测。计算得出在不影响准确性的情况下,肠杆菌科鉴定方案至少节省40%。截至1983年11月,预计每100次肠杆菌科鉴定可直接节省(劳动力和材料)成本约200.80美元。