Wei Yanqiu, Duan Yongcheng, Bi Yuhai, Wang Meng, Li Yunlong, Wang Xuan, Li Wei, Fan Wenhui, Wang Jing, Liu Wenjun, Yang Limin
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
College of Animal Science and Technology, Guangxi University, Nanning 530004, Guangxi, China.
Sheng Wu Gong Cheng Xue Bao. 2018 Dec 25;34(12):2025-2034. doi: 10.13345/j.cjb.180074.
Ebola virus (EBOV) is an extremely contagious pathogen first discovered in Africa associated with severe hemorrhagic disease in humans and nonhuman primates, which has resulted in at least 28 500 suspected cases and 11 300 confirmed deaths in 2014-2016 Ebola epidemic in West Africa. Rapid and sensitive detection of EBOV is the key to increasing the probability of survival and reducing infection rates in pandemic regions. Here, we report an ultrasensitive and instrument-free EBOV detection assay based on colloidal carbon immunochromatography. Carbon nanoparticle-labeled rabbit anti-EBOV-VP40 IgG were concentrated in the conjugate pad, monoclonal antibody (McAb, 4B7F9) against EBOV-VP40 and goat anti-rabbit IgG were immobilized on the nitrocellulose membrane with 2 μL/cm at a concentration of 1 mg/mL as test and control lines, respectively. Then the sample application pad, conjugate release pad, nitrocellulose membrane and absorbent pad were assembled into a lateral flow test strip. The test strip shows strong specificity against related viruses that share similar clinical symptoms and geographic range with EBOV, including marburg virus, influenza virus, yellow fever virus and dengue virus. In addition, 1 500 negative serums were tested with false-positive rate of 1.3‰ which significantly lower than that of ReEBOV™ colloidal gold test kit recommended by World Health Organization (WHO). The sensitivity of this strip was analyzed using inactivated EBOV with detection limit of 100 ng/mL (10⁶ copies/mL) which clearly higher than that of ReEBOV™ dipstick (10⁸ copies/mL). Furthermore, the strip showed excellent thermal stability characteristics in room temperature and could be as a point-of-care (POC), ultra-sensitive and specific promising candidate for EBOV serological screening in rural Africa or entry/exit ports.
埃博拉病毒(EBOV)是一种极具传染性的病原体,最初在非洲被发现,可导致人类和非人类灵长类动物患上严重出血热疾病。在2014 - 2016年西非埃博拉疫情中,已造成至少28500例疑似病例和11300例确诊死亡。快速灵敏地检测埃博拉病毒是提高疫区生存率和降低感染率的关键。在此,我们报道了一种基于胶体碳免疫层析的超灵敏且无需仪器的埃博拉病毒检测方法。碳纳米颗粒标记的兔抗埃博拉病毒VP40 IgG被浓缩于结合垫中,抗埃博拉病毒VP40单克隆抗体(McAb,4B7F9)和羊抗兔IgG分别以1 mg/mL的浓度、2 μL/cm的量固定于硝酸纤维素膜上作为检测线和对照线。然后将样品加样垫、结合物释放垫、硝酸纤维素膜和吸水垫组装成侧向流动试纸条。该试纸条对与埃博拉病毒具有相似临床症状和地理分布范围的相关病毒表现出很强的特异性,包括马尔堡病毒、流感病毒、黄热病病毒和登革病毒。此外,对1500份阴性血清进行检测,假阳性率为1.3‰,显著低于世界卫生组织(WHO)推荐的ReEBOV™胶体金检测试剂盒。使用灭活的埃博拉病毒分析该试纸条的灵敏度,检测限为100 ng/mL(10⁶拷贝/mL),明显高于ReEBOV™试纸(10⁸拷贝/mL)。此外,该试纸条在室温下表现出优异的热稳定性,可作为非洲农村地区或出入境口岸进行埃博拉病毒血清学筛查的即时检测(POC)、超灵敏且特异的有前景候选产品。