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作 者:罗巧[1] 李霜君[1] 肖彤洋 李马超[2] 刘海灿[2] 楼永良[1] 万康林[1] Luo Qiao;Li Shuangjun;Xiao Tongyang;Li Machao;Liu Haican;Lou Yongliang;Wan Kanglin(School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou 325035, China (Luo Q, Li S J, Lou YL, Wan KL;State Key Laboratory for Infectious Diseases Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China (Xiao TY, I4 MC, Liu HC, Wan KL)
机构地区:[1]温州医科大学检验医学院生命科学学院,325035 [2]中国疾病预防控制中心传染病预防控制所传染病预防控制国家重点实验室感染性疾病诊治协同创新中心,北京102206
出 处:《中华流行病学杂志》2018年第4期514-518,共5页Chinese Journal of Epidemiology
摘 要:目的 初步评价结核分枝杆菌4种新抗原Rv0432、Rv0674、Rv1566c和Rv1547的血清学诊断价值。方法 以结核分枝杆菌实验室标准参照菌株H37Rv全基因组DNA为模板PCR扩增Rv0432、Rv0674、Rv1566c基因的完整序列,Rv1547基因分为两段(Rv1547-1和Rv1547-2)扩增,与PET-32a表达载体构建重组质粒,重组蛋白利用亲和层析的方法进行纯化。待检测血清和BL21(DE3)菌体蛋白孵育进行预处理。各重组抗原用ELISA对151份待检血清(41份健康组血清和110份细菌学阳性结核患者组血清)进行IgG抗体检测。检测结果用受试者工作特征曲线对其诊断效能进行分析和评价。采用t检验比较目的蛋白在结核患者组和健康组的差异性。结果 成功克隆表达和纯化了蛋白Rv0432、Rv0674、Rv1566c、Rv1547-1和Rv1547-2,ELISA结果显示Rv0432、Rv0674、Rv1566c、Rv1547-1和Rv1547-2的敏感性、特异性、阳性预测值、阴性预测值、约登指数和曲线下面积分别为43.64%~92.73%、80.49%~92.68%、0.92~0.94、0.38~0.80、0.363~0.732和0.649~0.915。目的蛋白在结核组检测到的IgG抗体水平均大于健康组(P〈0.000 1)。结论 结核分枝杆菌新抗原Rv0432、Rv0674、Rv1566c、Rv1547-1和Rv1547-2具有良好的血清学检测价值,可作为结核病免疫学诊断的候选抗原。Objective To evaluate the serological diagnostic value of Mycobacterium (M.) tuberculosis four new antigens Rv0432, Rv0674, Rv1566c and Rv1547. Methods Rv0432, Rv0674, Rv1566c and Rv1547 were amplified from M. tuberculosis strain H37Rv genomic DNA by using PCR, among which Rv1547 was divided into two segments for amplification (Rv1547-1 and Rv1547-2). The segments were cloned into expression vector PET-32a while the recombinant proteins were purified by affinity chromatography. Serums were incubated with BL21 (DE3) proteins. Antibodies IgG against M. tuberculosis were tested with 151 serum samples (41 healthy people and 110 TB patients) by using ELISA. The diagnostic efficiency of antigens was analyzed by means of receiver operating characteristic curve. Difference of the objective proteins in TB patients and healthy controls was compared by t-test. Results Recombinant antigens Rv0432, Rv0674, Rv1566c, Rv1547-1 and Rv1547-2 were successfully expressed and purified. Results from ELISA showed that the sensitivity, specificity, positive predictive value, negative predictive value, Youden index and area under the curve of Rv0432, Rv0674, Rv1566c, Rv1547-1 and Rv1547-2, as 43.64%-92.73%, 80.49%-92.68%, 0.92-0.94, 0.38-0.80, 0.363-0.732 and 0.649-0.915. All the objective proteins showed significantly higher antibody levels in TB patients, when compared to the healthy controls (P〈0.000 1). Conclusion The newly identified antigens Rv0432, Rv0674, Rv1566c, Rv1547-1 and Rv1547-2 all performed well when being used for TB serological diagnosis, thus were expected to be new candidate antigens used for TB diagnosis.
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