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Differentiation of species in human beta-haemolytic group G streptococci using immunoglobulin Fc fragment receptor.

机译:使用免疫球蛋白Fc片段受体区分人β溶血性G组链球菌中的物种。

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摘要

AIMS: To assess the ability of human immunoglobulin Fc fragment binding activity to differentiate human biotype large colony group G streptococci from the group G "Streptococcus milleri group". METHODS: Fifty two isolates of large colony group G streptococci and 30 group G "S milleri group" strains were tested for their ability to bind fluorescein conjugated human IgG Fc fragments after acetone fixation. Immunoblotting with peroxidase labelled human Fc fragments after resolution of bacterial polypeptides by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) was performed for six large colony strains. RESULTS: All large colony group G streptococci showed positive Fc fragment binding whereas all "S milleri group" bacteria failed to bind Fc fragments when viewed by fluorescence microscopy. All six large colony strains showed similar immunoblot binding patterns. CONCLUSION: Immunoglobulin Fc fragment receptor content distinguishes the large colony group G streptococci from the group G "S milleri group" and mayhave a role in the rapid laboratory diagnosis of pharyngeal pathogens.
机译:目的:评估人免疫球蛋白Fc片段结合活性将人生物型大菌落组G链球菌与G组“米氏链球菌”区分开的能力。方法:测试了52个大菌落群G链球菌和30个G菌“ S milleri组”菌株的分离物,它们在丙酮固定后结合荧光素结合的人IgG Fc片段的能力。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离细菌多肽后,用过氧化物酶标记的人Fc片段进行免疫印迹分析。结果:当通过荧光显微镜观察时,所有大菌落群G链球菌均显示出阳性的Fc片段结合,而所有“ S milleri组”细菌均未结合Fc片段。所有六个大菌落菌株均显示出相似的免疫印迹结合模式。结论:免疫球蛋白Fc片段受体的含量将大菌落群G链球菌与G小组“ S Milleri组”区分开,并可能在快速诊断咽病原体中发挥作用。

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