Institute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, University of South China, Hengyang, Hunan 421001, China.
Nanyue Biopharmaceutical Co. Ltd., Hunan Province Innovative Training Base for Postgraduates, University of South China and Nanyue Biopharmaceutical Co. Ltd., Hengyang, Hunan 421001, China.
Life Sci. 2020 May 1;248:117444. doi: 10.1016/j.lfs.2020.117444. Epub 2020 Feb 19.
Nonhuman primates have been used to investigate pathogenic mechanisms and evaluate immune responses following Chlamydia trachomatis inoculation. This study aimed to systemically profile antibody responses to C. trachomatis infection in nonhuman primates.
Sera were obtained from 4 pig-tailed and 8 long-tailed macaques which were intravaginally or ocularly infected with live C. trachomatis organisms, and analyzed by C. trachomatis proteome array of antigens.
The sera from 12 macaques recognized total 172 C. trachomatis antigens. While 84 antigens were recognized by pig-tailed macaques intravaginally infected with serovar D strain, 125 antigens were recognized by long-tailed macaques ocularly infected with serovar A, and 37 antigens were recognized by both. Ocular inoculation with virulent A2497 strain induced antibodies to more antigens. Among the antigens uniquely recognized by A2497 strain infected macaques, outer membrane complex B antigen (OmcB) induced robust antibody response. Although macaques infected by less virulent A/HAR-13 strain failed to develop antibodies to OmcB, reinfection by A2497 strain induced high levels of antibodies to OmcB.
Proteome array has revealed a correlation of chlamydial infection invasiveness with chlamydial antigen immunogenicity, and identified antibody responses to OmcB potentially as biomarkers for invasive infection with C. trachomatis.
非人类灵长类动物已被用于研究沙眼衣原体感染后的致病机制和免疫反应。本研究旨在系统分析沙眼衣原体感染后非人类灵长类动物的抗体反应。
采集 4 只长尾猕猴和 8 只食蟹猕猴阴道或眼部感染活沙眼衣原体后的血清,并用沙眼衣原体蛋白质组芯片分析抗原。
12 只猕猴的血清共识别出 172 种沙眼衣原体抗原。84 种抗原被阴道感染 D 血清型菌株的食蟹猕猴识别,125 种抗原被眼部感染 A 血清型菌株的长尾猕猴识别,37 种抗原两者均能识别。眼部接种毒力更强的 A2497 株可诱导更多的抗原抗体。在 A2497 株感染猕猴特有的抗原中,外膜复合物 B 抗原(OmcB)诱导出强烈的抗体反应。虽然感染毒力较弱的 A/HAR-13 株的猕猴未能产生针对 OmcB 的抗体,但再次感染 A2497 株可诱导高水平的 OmcB 抗体。
蛋白质组芯片揭示了衣原体感染侵袭性与衣原体抗原免疫原性之间的相关性,并鉴定出针对 OmcB 的抗体反应可能是沙眼衣原体侵袭性感染的生物标志物。