Comanducci M, Manetti R, Bini L, Santucci A, Pallini V, Cevenini R, Sueur J M, Orfila J, Ratti G
Immunobiological Research Institute Siena, Italy.
Infect Immun. 1994 Dec;62(12):5491-7. doi: 10.1128/iai.62.12.5491-5497.1994.
We identified, by two-dimensional electrophoretic analysis and microsequencing, a protein of Chlamydia trachomatis elementary bodies which corresponds to the polypeptide (pgp3) encoded by open reading frame 3 (ORF3). Amino acid analysis showed that the first residue (Gly) found in the native protein is the one encoded by the second ORF3 codon, implying a typical bacterial removal of the first Met residue. Relatively large amounts of recombinant pgp3 (r-pgp3) in a stable, water-soluble form were obtained by overexpressing ORF3 in Escherichia coli and purifying the product from periplasmic extracts under nondenaturing conditions. These r-pgp3 preparations allowed specific detection of anti-pgp3 antibodies by enzyme-linked immunosorbent assay. Analysis of a group of 170 sera from healthy blood donors and from patients who were seropositive or -negative for C. trachomatis and Chlamydia pneumoniae showed that an immune response to pgp3 occurs in the majority (ca. 81%) of patients with sexually transmitted diseases who are seropositive for C. trachomatis and generally correlates with the response to cell surface antigens. No reaction between r-pgp3 and C. pneumoniae-positive sera was detected.
通过二维电泳分析和微量测序,我们鉴定出沙眼衣原体原体中的一种蛋白质,它与开放阅读框3(ORF3)编码的多肽(pgp3)相对应。氨基酸分析表明,天然蛋白质中发现的第一个残基(甘氨酸)是由第二个ORF3密码子编码的,这意味着典型的细菌去除第一个甲硫氨酸残基的过程。通过在大肠杆菌中过表达ORF3并在非变性条件下从周质提取物中纯化产物,获得了相对大量的稳定、水溶性形式的重组pgp3(r-pgp3)。这些r-pgp3制剂能够通过酶联免疫吸附测定法特异性检测抗pgp3抗体。对一组来自健康献血者以及沙眼衣原体和肺炎衣原体血清学阳性或阴性患者的170份血清进行分析,结果显示,在大多数(约81%)沙眼衣原体血清学阳性的性传播疾病患者中,存在对pgp3的免疫反应,并且通常与对细胞表面抗原的反应相关。未检测到r-pgp3与肺炎衣原体阳性血清之间的反应。