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Antigenic Determinants of Alpha-Like Proteins of Streptococcus agalactiae

机译:无乳链球菌α样蛋白的抗原决定簇。

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The majority of group B streptococcus (GBS) isolates express one or more of a family of surface-anchored proteins that vary by strain and that form ladder-like patterns on Western blotting due to large repeat units. These proteins, which are important as GBS serotype markers and as inducers of protective antibodies, include the alpha C (Cα) and R4 proteins and the recently described alpha-like protein 2 (Alp2), encoded by alp2, and Alp3, encoded by alp3. In this study, we examined antigenic determinants possessed by Alp2 and Alp3 by testing of antibodies raised in rabbits, mainly by using enzyme-linked immunosorbent assays (ELISA) and an ELISA absorption test. The results showed that Alp2 and Alp3 shared an antigenic determinant, which may be a unique immunological marker of the Alp variants of GBS proteins. Alp2, in addition, possessed an antigenic determinant which showed specificity for Alp2 and a third determinant which showed serological cross-reactivity with Cα. Alp3, in addition to the determinant common to Alp2 and Alp3, harbored an antigenic site which also was present in the R4 protein, whereas no Alp3-specific antigenic site was detected. These ELISA-based results were confirmed by Western blotting and a fluorescent-antibody test. The results are consistent with highly complex antigenic structures of the alpha-like proteins in a fashion which is in agreement with the recently described structural mosaicism of the alp2 and alp3 genes. The results are expected to influence GBS serotyping, immunoprotection studies, and GBS vaccine developments.
机译:大多数B组链球菌(GBS)分离物表达一种或多种表面锚定蛋白家族,这些蛋白因菌株而异,并且由于较大的重复单元而在Western印迹上形成阶梯状图案。这些蛋白质作为GBS血清型标记和保护性抗体的诱导物非常重要,包括由 alp2 编码的alpha C(Cα)和R4蛋白以及最近描述的alpha-like蛋白2(Alp2)。以及由 alp3 编码的Alp3。在这项研究中,我们主要通过使用酶联免疫吸附测定(ELISA)和ELISA吸收测试,通过测试兔中产生的抗体来检查Alp2和Alp3拥有的抗原决定簇。结果表明,Alp2和Alp3共享一个抗原决定簇,这可能是GBS蛋白Alp变体的独特免疫学标记。此外,Alp2具有对Alp2表现出特异性的抗原决定簇和与Cα发生血清学交叉反应的第三个决定簇。除Alp2和Alp3共有的决定因素外,Alp3还包含一个抗原位点,该位点也存在于R4蛋白中,而未检测到Alp3特异性抗原位点。这些基于ELISA的结果通过Western印迹和荧光抗体测试得到证实。该结果与α-样蛋白的高度复杂的抗原结构相一致,这与最近描述的 alp2 alp3 基因的结构镶嵌一致。预期结果将影响GBS血清分型,免疫保护研究和GBS疫苗的开发。

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