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首页> 外文期刊>Journal of Clinical Microbiology >Comparison of the Phadebact Gonococcus Test with the rapid fermentation method.
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Comparison of the Phadebact Gonococcus Test with the rapid fermentation method.

机译:Phadebact淋球菌试验与快速发酵法的比较。

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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.
机译:将Phadebact淋球菌试验(Pharmacia Diagnostics,Piscataway,NJ),一种凝集技术与Kellogg and Turner的快速发酵方法(DS Kellogg,Jr.和EM Turner,Appl.Microbiol.25:550--552, 1973)。根据以下标准,在马丁·刘易斯培养基上分离出的总共93种细菌被确定为淋病奈瑟菌:革兰氏阴性双球菌的存在,氧化酶阳性以及快速发酵方法中的适当反应。然后用Phadebact检验对这93个分离株进行血清学检验。在最初的46种淋病奈瑟氏球菌中尝试了直接方法。 39%的人遇到了翻译结果的困难。此后,对另外的47个淋病奈瑟氏球菌分离株采用了另一种煮沸方法,其中2个分离株产生无法解释的结果。将所有93个分离株在脱脂牛奶中于-25摄氏度下冷冻最多2个月。将这些分离株解冻,并用交替煮沸程序重新键入,其中97%被确认为淋病奈瑟氏球菌。此外,还使用相似的技术测试了33株脑膜炎奈瑟氏菌分离株,14株奈瑟氏菌和7种莫拉氏菌。没有观察到阳性反应。进行了使用5、10和20微升淋球菌试剂的成本效益研究,以降低测试成本。当使用10和20微升试剂时,在解释反应时没有遇到困难。当使用5微升试剂时,凝集技术难以读取。

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