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法代巴克氏淋球菌检测与快速发酵法的比较。

Comparison of the Phadebact Gonococcus Test with the rapid fermentation method.

作者信息

Futrovsky S L, Gaydos C A, Keiser J

出版信息

J Clin Microbiol. 1981 Jul;14(1):89-93. doi: 10.1128/jcm.14.1.89-93.1981.

Abstract

The Phadebact Gonococcus Test (Pharmacia Diagnostics, Piscataway, N.J.), a coagglutination technique, was compared with the rapid fermentation method of Kellogg and Turner (D. S. Kellogg, Jr., and E. M. Turner, Appl. Microbiol. 25: 550--552, 1973). A total of 93 organisms isolated on Martin-Lewis media were determined to be Neisseria gonorrhoeae based on the following criteria: presence of gram-negative diplococci, oxidase positivity, and appropriate reaction in the rapid fermentation method. These 93 isolates were then serologically tested with the Phadebact test. The direct method was attempted on the first 46 N. gonorrhoeae isolates. Difficulty in interpreting results was encountered in 39%. Thereafter, the alternate method of boiling was instituted on an additional 47 N. gonorrhoeae isolates, with 2 isolates producing noninterpretable results. All 93 isolates were frozen for a maximum of 2 months in skim milk at -25 degrees C. These isolates were thawed and retyped with the alternate boiling procedure, with 97% being confirmed as N. gonorrhoeae. In addition, 33 Neisseria meningitidis isolates, 14 Neisseria species, and 7 Moraxella species were tested with similar techniques. No positive reactions were observed. A cost effectiveness study using 5, 10, and 20 microliters of the gonococcal reagent was undertaken to reduce the cost of the test. When 10 and 20 microliters of reagent were used, no difficulty was encountered in interpreting the reaction. The coagglutination technique was difficult to read when 5 microliters of reagent was used.

摘要

将凝固法的Phadebact淋球菌检测试验(Pharmacia诊断公司,新泽西州皮斯卡塔韦)与Kellogg和Turner的快速发酵法(小D.S. Kellogg和E.M. Turner,《应用微生物学》25: 550 - 552,1973年)进行了比较。根据以下标准,共确定在Martin-Lewis培养基上分离出的93株菌为淋病奈瑟菌:革兰氏阴性双球菌的存在、氧化酶阳性以及快速发酵法中的适当反应。然后用Phadebact试验对这93株分离株进行血清学检测。对最初的46株淋病奈瑟菌分离株尝试了直接法。39%的结果难以解读。此后,对另外47株淋病奈瑟菌分离株采用了煮沸替代法,有2株产生了无法解读的结果。所有93株分离株在-25℃的脱脂乳中最多冷冻2个月。将这些分离株解冻,并用煮沸替代程序重新分型,97%被确认为淋病奈瑟菌。此外,用类似技术对33株脑膜炎奈瑟菌分离株、14株奈瑟菌属菌株和7株莫拉克斯氏菌属菌株进行了检测。未观察到阳性反应。进行了一项成本效益研究,使用5、10和20微升的淋球菌试剂以降低检测成本。当使用10微升和20微升试剂时,解读反应没有困难。当使用5微升试剂时,凝固法难以读取结果。

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