Jalali Tahmineh, Salehi-Vaziri Mostafa, Pouriayevali Mohammad Hassan, Mousavi Gargari Seyed Latif
Department of Biology, Faculty of Basic Sciences, Shahed University, Tehran, Iran.
Department of Arboviruses and Viral Hemorrhagic Fevers (National Reference Laboratory), Pasteur Institute of Iran, Tehran, Iran.
Iran Biomed J. 2019 Nov;23(6):379-87. doi: 10.29252/ibj.23.6.379. Epub 2019 May 20.
Crimean-Congo hemorrhagic fever (CCHF) is an acute viral zoonotic disease, with a mortality rate of 30-50%. There is no approved vaccine or any specific antiviral treatment for CCHF; therefore, the rapid diagnosis seems to be crucial for both efficient supportive therapy and control of infection spread. In this study, the potency of recombinant nucleoprotein of virus expressed in prokaryotic system was investigated for diagnosis of the infection.
The DNA sequence of complete nucleoprotein ORF was codon optimized based on E. coli codon usage and synthesized commercially. The gene was subcloned in pCA4 vector and expressed in E. coli BL21 (DE3). Refolding and simultaneous purification of nucleoprotein were performed using protein folding liquid chromatography method. The recombinant nucleoprotein was analyzed by Western blotting, ELISA, immunofluorescence assay, and circular dichroism. Forty eight human samples, in three IgM positive and three negative control groups, were evaluated using recombinant nucleoprotein in a capture ELISA setting. Serum from healthy individuals, those suspected to viral hemorrhagic fevers, and positive samples of Chikungunya and Dengue were considered as negative controls.
The existence and structure of recombinant nucleoprotein were verified and confirmed. Capture IgM ELISA detected all positive samples (sensitivity of 100%), but none of the 25 negative samples was detected as positive (specificity of 100%). The test also detected all the included genotypes of virus.
Our recombinant nucleoprotein can be used in IgM capture ELISA for easy and efficient detection of CCHF in any lab in endemic regions.
克里米亚-刚果出血热(CCHF)是一种急性病毒性人畜共患病,死亡率为30%-50%。目前尚无批准用于CCHF的疫苗或任何特异性抗病毒治疗方法;因此,快速诊断对于有效的支持性治疗和控制感染传播似乎至关重要。在本研究中,对原核系统中表达的病毒重组核蛋白用于感染诊断的效能进行了研究。
基于大肠杆菌密码子使用情况对完整核蛋白开放阅读框的DNA序列进行密码子优化,并进行商业合成。该基因亚克隆至pCA4载体中,并在大肠杆菌BL21(DE3)中表达。使用蛋白质折叠液相色谱法进行核蛋白的复性和同步纯化。通过蛋白质印迹法、酶联免疫吸附测定(ELISA)、免疫荧光测定和圆二色性对重组核蛋白进行分析。在捕获ELISA实验中,使用重组核蛋白对48份人类样本进行评估,分为3个IgM阳性和3个阴性对照组。来自健康个体、疑似病毒性出血热患者的血清以及基孔肯雅热和登革热阳性样本被视为阴性对照。
重组核蛋白的存在和结构得到验证和确认。捕获IgM ELISA检测到所有阳性样本(灵敏度为100%),但25份阴性样本中无一被检测为阳性(特异性为100%)。该检测还检测到了所有纳入研究的病毒基因型。
我们的重组核蛋白可用于IgM捕获ELISA,以便在流行地区的任何实验室轻松、高效地检测CCHF。