O'Hara Caroline M, Miller J Michael
Epidemiology and Laboratory Branch, Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
J Clin Microbiol. 2002 Oct;40(10):3750-2. doi: 10.1128/JCM.40.10.3750-3752.2002.
The MicroScan Rapid Neg ID3 panel is designed for the identification of Enterobacteriaceae and nonenteric glucose-fermenting and nonfermenting gram-negative bacilli. We evaluated this panel for its ability to identify gram-negative non-Enterobacteriaceae bacteria. A total of 134 strains, representing 26 genera and 42 species, were taken from storage at -70(o)C, passaged three times before testing, and inoculated into the panels according to the manufacturer's directions before being inserted into a Walk/Away 96 instrument loaded with version 22.28 software. At the end of the initial 2.5-h incubation period, 89 isolates (66.4%) were correctly identified at a probability level of > or =85%. After additional testing recommended by the manufacturer was completed, another 11 isolates (8.2%) were correctly identified at probability levels of > or =85%. Twenty-five (18.7%) isolates were correctly identified after additional testing, but the probability levels were less than 85%. Two isolates were unidentified, and seven (5.2%) were incorrectly identified. The seven misidentified strains were not concentrated in any one genus. With an accuracy approaching 75%, this product may be used for the identification of the commonly isolated non-Enterobacteriaceae bacteria but may present problems in identification of other non-glucose-fermenting gram-negative bacilli.
MicroScan快速阴性鉴定ID3板专为鉴定肠杆菌科细菌、非肠道葡萄糖发酵菌和非发酵革兰氏阴性杆菌而设计。我们评估了该鉴定板对革兰氏阴性非肠杆菌科细菌的鉴定能力。从-70℃保存的菌株中选取了总共134株,代表26个属和42个种,在测试前传代三次,并按照制造商的说明接种到鉴定板中,然后插入装有22.28版软件的Walk/Away 96仪器中。在最初2.5小时的培养期结束时,89株分离菌(66.4%)在概率水平≥85%时被正确鉴定。在完成制造商推荐的额外测试后,又有11株分离菌(8.2%)在概率水平≥85%时被正确鉴定。25株(18.7%)分离菌在额外测试后被正确鉴定,但概率水平低于85%。有2株分离菌未被鉴定,7株(5.2%)被错误鉴定。这7株被错误鉴定的菌株并不集中在任何一个属中。该产品的准确率接近75%,可用于鉴定常见的非肠杆菌科细菌,但在鉴定其他非葡萄糖发酵革兰氏阴性杆菌时可能会出现问题。