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Identification of Novel Mycobacterium tuberculosis Antigens with Potential as Diagnostic Reagents or Subunit Vaccine Candidates by Comparative Genomics

机译:比较基因组学鉴定具有诊断试剂或亚基疫苗候选潜力的新型结核分枝杆菌抗原

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摘要

An independent review for the British government has concluded that the development of a cattle vaccine against Mycobacterium bovis holds the best long-term prospects for tuberculosis control in British herds. The development of complementary diagnostic tests to differentiate between vaccinated and infected animals is necessary to allow the continuation of test-and-slaughter-based control policies alongside vaccination. Vaccination with M. bovis bacillus Calmette-Guérin (BCG), the only available vaccine, results in tuberculin purified protein derivative sensitivity and has shown varying vaccine efficacies in cattle. Thus, identification of more-specific reagents to distinguish between vaccination and infection, as well as the identification of subunit vaccine candidates for improved tuberculosis vaccines, is a research priority. In the present study, we applied comparative genomics to identify M. bovis-Mycobacterium tuberculosis antigens whose genes had been deleted in BCG Pasteur. In total, 13 open reading frames (ORFs) from the RD1, RD2, and RD14 regions of the M. tuberculosis genome were selected. Pools of overlapping peptides spanning these ORFs were tested in M. bovis-infected (n = 22), BCG-vaccinated (n = 6), and unvaccinated (n = 10) control cattle. All were recognized in infected cattle, with responder frequencies varying between 16 and 86%. In particular, eight highly immunogenic antigens were identified whose potentials as diagnostic reagents or as subunit vaccines warrant further study (Rv1983, Rv1986, Rv3872, Rv3873, Rv3878, Rv3879c, Rv1979c, and Rv1769).
机译:英国政府的一项独立审查得出的结论是,针对牛分枝杆菌的牛疫苗的开发在英国人群中控制结核病具有最佳的长期前景。必须发展补充诊断测试以区分接种疫苗的动物和感染的动物,以允许在接种疫苗的同时继续实施基于测试和屠宰的控制策略。用唯一可用的牛分枝杆菌卡介苗(BCG)进行疫苗接种会导致结核菌素纯化的蛋白衍生物敏感,并显示出牛的疫苗效力不同。因此,鉴定更具特异性的试剂以区分疫苗接种和感染,以及鉴定改良的结核疫苗的亚单位疫苗候选物是研究的重点。在本研究中,我们应用比较基因组学来鉴定牛分枝杆菌-结核分枝杆菌抗原,其基因已在BCG Pasteur中删除。总共从结核分枝杆菌基因组的RD1,RD2和RD14区域选择了13个开放阅读框(ORF)。在牛分枝杆菌感染(n = 22),接种卡介苗(n = 6)和未接种牛(n = 10)的对照牛中测试了跨越这些ORF的重叠肽库。所有这些均在感染的牛中识别,应答频率在16%至86%之间。特别是,鉴定出了八种高度免疫原性抗原,它们有潜力作为诊断试剂或亚单位疫苗,需要进一步研究(Rv1983,Rv1986,Rv3872,Rv3873,Rv3878,Rv3879c,Rv1979c和Rv1769)。

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