Laughon B E, Ehret J M, Tanino T T, Van der Pol B, Handsfield H H, Jones R B, Judson F N, Hook E W
Division of Infectious Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Clin Microbiol. 1987 Dec;25(12):2388-90. doi: 10.1128/jcm.25.12.2388-2390.1987.
We evaluated a monoclonal fluorescent-antibody (FA) reagent (Neisseria gonorrhoeae Culture Confirmation Test; Syva Co., Palo Alto, Calif.) for confirmation of N. gonorrhoeae isolates obtained from clinics for sexually transmitted diseases in four cities. The FA test was performed in parallel with established confirmation procedures on all organisms growing on 773 primary culture plates of modified Thayer-Martin agar. All N. gonorrhoeae isolates reacted with the FA reagent and produced a bright, easily interpretable fluorescence. The FA test correctly identified 533 N. gonorrhoeae isolates from 474 patients and did not react with 90 N. meningitidis or with 213 non-Neisseria isolates. In one city (Baltimore), Gonochek II (Du Pont Co., Wilmington, Del.) failed to identify four N. gonorrhoeae isolates reactive with the FA reagent and confirmed as N. gonorrhoeae by Phadebact (Pharmacia Inc., Piscataway, N.J.) and acid production from sugars. The FA test was rapid and specific and could be performed directly from primary isolation plates. The test requires 1 h to perform and is applicable to mixed-flora cultures.
我们评估了一种单克隆荧光抗体(FA)试剂(淋病奈瑟菌培养确认试验;Syva公司,加利福尼亚州帕洛阿尔托),用于确认从四个城市的性传播疾病诊所分离得到的淋病奈瑟菌。FA试验与既定的确认程序同时对在改良的Thayer-Martin琼脂的773个原代培养平板上生长的所有微生物进行检测。所有淋病奈瑟菌分离株均与FA试剂发生反应,并产生明亮、易于解读的荧光。FA试验正确鉴定出474例患者中的533株淋病奈瑟菌分离株,且不与90株脑膜炎奈瑟菌或213株非奈瑟菌分离株发生反应。在一个城市(巴尔的摩),Gonochek II(杜邦公司,特拉华州威尔明顿)未能鉴定出4株与FA试剂反应且经Phadebact(法玛西亚公司,新泽西州皮斯卡塔韦)和糖产酸确认的淋病奈瑟菌分离株。FA试验快速且特异,可直接从原代分离平板上进行。该试验需耗时1小时完成,适用于混合菌群培养。