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Phase Variation among Major Surface Antigens of Mycoplasma penetrans

机译:支原体支原体主要表面抗原之间的相变

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摘要

The pathogenicity and prevalence of Mycoplasma penetrans, a Mycoplasma species recently isolated from humans, are still debated. A major P35 antigen, which is used as target epitope in serological assays, was shown to be a phase-variable lipid-associated membrane protein (LAMP). In this study, we performed a comparative analysis of the LAMP patterns from five M. penetrans clinical isolates and from the type strain. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles and immunoblots with sera serially collected from an M. penetrans-infected patient indicated that these strains expressed different LAMP repertoires. Furthermore, the intraclonal variation in the expression of LAMPs (P34A, P34B, P35, and P38) was monitored by immunoblot analysis with three specific monoclonal antibodies (MAbs) developed in this study and MAb 7 to P35. The phase variation of these LAMPs occurs in an independent manner, with frequencies of variation ranging from 10−2 to 10−4 per cell per generation. Consistent with their amphipathic nature, the P34B and P38 antigens were found exposed at the cell surface. The DNA sequence encoding the P38 antigen was defined and found to be related to those of the P35 gene and other putative LAMP-encoding genes, suggesting that these variable antigens are encoded by a family of related genes. Finally, the serum samples from an M. penetrans-infected patient contained antibodies that reacted with a P36 antigen expressed in different M. penetrans strains but not in the isolate recovered from this patient. This result suggested that in vivo phase variation of P36 occurred, which would support a role for these LAMP variations in avoiding the host's immune vigilance.
机译:支原体支原体(一种最近从人类中分离出来的支原体)的致病性和流行程度仍在争论中。主要的P35抗原(在血清学检测中用作目标表位)显示为相变脂质相关膜蛋白(LAMP)。在这项研究中,我们对来自五种M. penetrans临床分离株和类型菌株的LAMP模式进行了比较分析。十二烷基硫酸钠-聚丙烯酰胺钠凝胶电泳图谱和带有免疫印迹的血清,从血清中检测到,这些感染株均来自于经peetrans感染的患者,表明这些菌株表达了不同的LAMP组成。此外,使用本研究开发的三种特异性单克隆抗体(MAb)和MAb 7至P35通过免疫印迹分析监测LAMPs(P34A,P34B,P35和P38)表达的克隆内变异。这些LAMP的相位变化以独立的方式发生,每代每细胞的变化频率范围为10 -2 至10 -4 。与它们的两亲性质一致,发现P34B和P38抗原暴露在细胞表面。定义了编码P38抗原的DNA序列,发现该序列与P35基因和其他假定的LAMP编码基因的DNA序列相关,表明这些可变抗原由相关基因家族编码。最后,来自戊型肝炎支原体感染患者的血清样品含有与在不同的戊型肝炎支原体菌株中表达但未在从该患者回收的分离物中表达的P36抗原反应的抗体。该结果表明P36在体内发生了相变,这将支持这些LAMP变异在避免宿主的免疫警惕中的作用。

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