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沙眼衣原体一种编码新型28 kDa抗原的质粒基因的表达。

Expression of a plasmid gene of Chlamydia trachomatis encoding a novel 28 kDa antigen.

作者信息

Comanducci M, Cevenini R, Moroni A, Giuliani M M, Ricci S, Scarlato V, Ratti G

机构信息

Immunobiological Research Institute Siena (IRIS), Italy.

出版信息

J Gen Microbiol. 1993 May;139(5):1083-92. doi: 10.1099/00221287-139-5-1083.

Abstract

Plasmid pCT is present in essentially all isolates of Chlamydia trachomatis and may encode factors important for survival in the natural environment. However, no pCT-associated phenotype has been described so far. With the purpose of investigating the possibility of a role of pCT in C. trachomatis pathogenicity we examined the expression of an ORF (ORF3), potentially encoding a 28 kDa polypeptide (pgp3). Analysis of RNA extracted from chlamydia-infected Vero cells detected ORF3-specific transcripts, from 20 h post-infection onwards, mainly as discrete RNA species of 1390 nucleotides comprising the downstream ORF4 sequence. ORF3 DNA was cloned and expressed in Escherichia coli as a 39 kDa fusion protein (MS2/pgp3). Antibodies raised against purified MS2/pgp3, specifically recognized a 28 kDa protein on Western blots of protein from purified chlamydial elementary bodies (EBs). The same antibodies detected chlamydial inclusions in methanol-fixed infected cells by immunofluorescence. Western blot analysis of EBs extracted with 2% Sarkosyl, showed that a large proportion of the 28 kDa antigen is associated with the detergent-insoluble ('membrane') fraction. Antibodies recognizing pgp3 epitopes were detected in sera from patients with chlamydial infections, but not in sero-negative control sera. The finding support the hypothesis that pCT may provide a function related to chlamydial cell physiology.

摘要

质粒pCT基本上存在于沙眼衣原体的所有分离株中,可能编码对在自然环境中生存至关重要的因子。然而,迄今为止尚未描述与pCT相关的表型。为了研究pCT在沙眼衣原体致病性中发挥作用的可能性,我们检测了一个可能编码28 kDa多肽(pgp3)的开放阅读框(ORF3)的表达。对从衣原体感染的Vero细胞中提取的RNA进行分析,在感染后20小时及以后检测到ORF3特异性转录本,主要是包含下游ORF4序列的1390个核苷酸的离散RNA种类。ORF3 DNA被克隆并在大肠杆菌中表达为39 kDa融合蛋白(MS2/pgp3)。针对纯化的MS2/pgp3产生的抗体,在纯化的衣原体原体(EBs)蛋白质的蛋白质免疫印迹上特异性识别一种28 kDa的蛋白质。相同的抗体通过免疫荧光检测甲醇固定的感染细胞中的衣原体包涵体。用2% Sarkosyl提取的EBs的蛋白质免疫印迹分析表明,大部分28 kDa抗原与去污剂不溶性(“膜”)部分相关。在衣原体感染患者的血清中检测到识别pgp3表位的抗体,但在血清阴性对照血清中未检测到。这一发现支持了pCT可能提供与衣原体细胞生理学相关功能的假说。

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