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使用法德巴克链球菌试验对初代分离平板上的β溶血性链球菌进行直接平板血清学分群。

Direct-plate serological grouping of beta-hemolytic streptococci from primary isolation plates with the Phadebact streptococcus test.

作者信息

Slifkin M, Engwall C, Pouchet G R

出版信息

J Clin Microbiol. 1978 Apr;7(4):356-60. doi: 10.1128/jcm.7.4.356-360.1978.

Abstract

The grouping of beta-hemolytic streptococcal isolates by a new direct-plate procedure employing Phadebact Streptococcus Test reagents was compared with the results obtained with the 4- and 24-h Phadebact grouping procedure and with the Lancefield grouping obtained with a capillary precipitin test. The new procedure employed a modification of the Phadebact procedure that permitted the grouping of streptococci on glass slides with a minimum of five primary isolated colonies. When only five to eight colonies were available for direct testing with each Phadebact reagent, coagglutination was better manifested when the colonies were disaggregated on a glass slide in a loopful of Tween 80 solution. Further enhancement of the coagglutination reaction was effected when the respective Phadebact reagents were employed in relatively small volumes. The direct-plate procedure permitted the correct identification of 127 out of 129 betahemolytic isolates. The 4-h method correctly identified 192 of the 200 streptococci tested. All of the 200 isolates tested by the 24-h procedure and the Lancefield grouping were correctly identified. The direct-plate Phadebact procedure affords the clinical microbiologist a rapid and reliable means of identifying groups A, B, C, and G beta-hemolytic streptococci. When sufficient numbers of primary colonies are not available for the direct procedure, the 4- or 24-h procedures may be employed.

摘要

采用法代巴克链球菌检测试剂的一种新的直接平板法对β溶血性链球菌分离株进行分组,并与4小时和24小时法代巴克分组法以及用毛细管沉淀试验进行的兰斯菲尔德分组法所获得的结果进行比较。新方法对法代巴克方法进行了改进,允许在载玻片上对链球菌进行分组,所用的初代分离菌落最少为5个。当每种法代巴克试剂仅能获得5至8个菌落用于直接检测时,将菌落在载玻片上用一小环吐温80溶液进行分散时,凝集反应表现得更好。当使用相对少量的相应法代巴克试剂时,凝集反应会进一步增强。直接平板法能够正确鉴定129株β溶血性分离株中的127株。4小时方法正确鉴定了所检测的200株链球菌中的192株。通过24小时法和兰斯菲尔德分组法检测的所有200株分离株均被正确鉴定。直接平板法代巴克程序为临床微生物学家提供了一种快速可靠的方法来鉴定A、B、C和G组β溶血性链球菌。当没有足够数量的初代菌落用于直接程序时,可以采用4小时或24小时程序。

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