Hilker H S, Solberg M
Appl Microbiol. 1973 Nov;26(5):751-6. doi: 10.1128/am.26.5.751-756.1973.
The reliability of the enrichment serology (ES), fluorescent antibody (FA), and a combination of the FA and ES procedures for the detection of salmonellae were compared to the Salmonella cultural procedure outlined in the U.S. Food and Drug Administration's Bacteriological Analytical Manual (BAM). A total of 126 subsamples from 22 different products were analyzed. By utilizing the BAM procedure as the reference standard, a total of 66 samples were positive for salmonellae. Within 44 h approximately 65% of the Salmonella-negative samples could be cleared by the FA test. At the end of 50 h 97% of the Salmonella-negative samples could be cleared by the combination FA-ES test. The FA procedure detected all 66 BAM positives but exhibited a high incidence of presumptive positives which were cultural negatives. The ES procedure detected 64 of the 66 BAM positives but exhibited a low incidence of presumptive positives which were cultural negatives. Incorporating positive FA and positive ES results in a combination FA-ES technique revealed that FA-ES positives were statistically equivalent to BAM positives.
将富集血清学(ES)、荧光抗体(FA)以及FA与ES联合检测沙门氏菌的方法的可靠性,与美国食品药品监督管理局《细菌学分析手册》(BAM)中概述的沙门氏菌培养方法进行了比较。对来自22种不同产品的126个亚样本进行了分析。以BAM方法作为参考标准,共有66个样本沙门氏菌检测呈阳性。在44小时内,约65%的沙门氏菌阴性样本可通过FA检测排除。在50小时结束时,97%的沙门氏菌阴性样本可通过FA-ES联合检测排除。FA方法检测出了所有66个BAM阳性样本,但出现了大量推定阳性结果,而这些样本培养结果为阴性。ES方法检测出了66个BAM阳性样本中的64个,但推定阳性结果(培养阴性)的发生率较低。在FA-ES联合技术中纳入阳性FA和阳性ES结果显示,FA-ES阳性结果在统计学上与BAM阳性结果相当。