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穿透支原体主要表面抗原的相变

Phase variation among major surface antigens of Mycoplasma penetrans.

作者信息

Röske K, Blanchard A, Chambaud I, Citti C, Helbig J H, Prevost M C, Rosengarten R, Jacobs E

机构信息

Institut für Medizinische Mikrobiologie und Hygiene, Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, D-01307 Dresden, Germany.

出版信息

Infect Immun. 2001 Dec;69(12):7642-51. doi: 10.1128/IAI.69.12.7642-7651.2001.

Abstract

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.

摘要

穿透支原体是最近从人类分离出的一种支原体,其致病性和流行情况仍存在争议。一种主要的P35抗原,在血清学检测中用作靶表位,已被证明是一种相变脂质相关膜蛋白(LAMP)。在本研究中,我们对五株穿透支原体临床分离株和标准菌株的LAMP模式进行了比较分析。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳图谱以及从一名穿透支原体感染患者连续采集的血清进行的免疫印迹表明,这些菌株表达不同的LAMP库。此外,通过使用本研究中制备的三种特异性单克隆抗体(MAb)和抗P35的单克隆抗体7进行免疫印迹分析,监测了LAMP(P34A、P34B、P35和P38)表达的克隆内变异。这些LAMP的相变以独立的方式发生,变异频率为每代每个细胞10^(-2)至10^(-4)。与它们的两亲性性质一致,发现P34B和P38抗原暴露于细胞表面。确定了编码P38抗原的DNA序列,发现其与P35基因和其他推定的LAMP编码基因的序列相关,这表明这些可变抗原由一个相关基因家族编码。最后,一名穿透支原体感染患者的血清样本中含有与不同穿透支原体菌株中表达但在从该患者分离出的菌株中不表达的P36抗原发生反应的抗体。这一结果表明P36在体内发生了相变变化,这将支持这些LAMP变异在逃避宿主免疫监视中的作用。

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