Shrivastava Neha, Shrivastava Ambuj, Ninawe Sandeep M, Sharma Shashi, Kumar Jyoti S, Alam Syed Imteyaz, Kanani Amit, Sharma Sushil Kumar, Dash Paban Kumar
Division of Virology, Defence Research and Development Establishment, Gwalior, India.
Division of Biotechnology, Defence Research and Development Establishment, Gwalior, India.
Front Microbiol. 2019 Aug 23;10:1822. doi: 10.3389/fmicb.2019.01822. eCollection 2019.
Crimean-Congo hemorrhagic fever (CCHF) is a re-emerging zoonotic viral disease prevalent in many parts of Asia, Europe, and Africa. The causative agent, Crimean-Congo hemorrhagic fever orthonairovirus (CCHFV), is transmitted through hard ticks. Tick vectors especially belonging to the species serve as the reservoir and amplifying host. The vertebrate animals including sheep, goat, and bovine act as a short-lasting bridge linking the virus and ticks. CCHFV causes fatal hemorrhagic fever in humans. Humans are usually infected with CCHFV either through the bite of infected ticks or by close contact with infected animals. Immunological assays, primarily enzyme-linked immunosorbent assay (ELISA) using whole viral antigen, are widely used for serosurveillance in animals. However, the whole virus antigen poses a high biohazard risk and can only be produced in biosafety level 4 laboratories. The present study focuses on the development and evaluation of safe, sensitive, and specific IgG indirect enzyme-linked immunosorbent assay (iELISA) using recombinant nucleoprotein (NP) of CCHF virus as an antigen. The codon-optimized NP gene sequence was synthesized, cloned, and expressed in pET28a+ vector. The recombinant NP was purified to homogeneity by affinity chromatography and characterized through Western blot and MALDI-TOF/MS analysis. The characterized protein was used to develop an indirect IgG microplate ELISA using a panel of animal sera. The in-house ELISA was comparatively evaluated vis-à-vis a commercially available ELISA kit (Vector-Best, Russia) with 76 suspected samples that revealed a concordance of 90% with a sensitivity and specificity of 79.4 and 100%, respectively. The precision analysis revealed that the assay is robust and reproducible in different sets of conditions. Further, the assay was used for serosurveillance in ruminants from different regions of India that revealed 18% seropositivity in ruminants, indicating continued circulation of virus in the region. The findings suggest that the developed IgG iELISA employing recombinant NP is a safe and valuable tool for scalable high-throughput screening of CCHFV-specific antibodies in multiple species.
克里米亚-刚果出血热(CCHF)是一种再次出现的人畜共患病毒性疾病,在亚洲、欧洲和非洲的许多地区流行。病原体克里米亚-刚果出血热正纳罗病毒(CCHFV)通过硬蜱传播。蜱虫媒介,特别是属于该物种的蜱虫,充当储存宿主和扩增宿主。包括绵羊、山羊和牛在内的脊椎动物作为连接病毒和蜱虫的短暂桥梁。CCHFV可导致人类致命性出血热。人类通常通过被感染蜱虫叮咬或与受感染动物密切接触而感染CCHFV。免疫测定,主要是使用全病毒抗原的酶联免疫吸附测定(ELISA),广泛用于动物血清监测。然而,全病毒抗原具有很高的生物危害风险,只能在生物安全4级实验室生产。本研究重点关注以CCHF病毒重组核蛋白(NP)为抗原的安全、灵敏且特异的IgG间接酶联免疫吸附测定(iELISA)的开发和评估。对密码子优化的NP基因序列进行合成、克隆,并在pET28a +载体中表达。重组NP通过亲和层析纯化至同质,并通过蛋白质印迹和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF/MS)分析进行表征。使用一组动物血清,将经表征的蛋白质用于开发间接IgG微孔板ELISA。使用76份疑似样本,将自制ELISA与市售ELISA试剂盒(俄罗斯Vector-Best)进行比较评估,结果显示一致性为90%,灵敏度和特异性分别为79.4%和100%。精密度分析表明,该测定在不同条件下具有稳健性和可重复性。此外,该测定用于对印度不同地区反刍动物的血清监测,结果显示反刍动物的血清阳性率为18%,表明该地区病毒持续传播。研究结果表明,所开发的采用重组NP的IgG iELISA是一种安全且有价值的工具,可用于对多种物种的CCHFV特异性抗体进行可扩展高通量筛选。