Wang Yang, Dai Junfei, Liu Yongsheng, Yang Jifei, Hou Qian, Ou Yunwen, Ding Yaozhong, Ma Bing, Chen Haotai, Li MiaoMiao, Sun Yuefeng, Zheng Haixue, Zhang Keshan, Wubshet Ashenafi Kiros, Zaberezhny Alexei D, Aliper Taras I, Tarasiuk Kazimierz, Pejsak Zygmunt, Liu Zhijie, Zhang Yongguang, Zhang Jie
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Department of Basic and Diagnostic Sciences, College of Veterinary Sciences, Mekelle University, Mekelle, Ethiopia.
Front Microbiol. 2021 Apr 23;12:609821. doi: 10.3389/fmicb.2021.609821. eCollection 2021.
African swine fever (ASF) has caused huge economic losses to the swine industry worldwide. Since there is no commercial ASF vaccine available, an early diagnosis is extremely important to prevent and control the disease. In this study, ASF virus (ASFV) capsid protein-encoding gene (p72) was selected and used to design primers for establishing a one-step visual loop-mediated isothermal amplification (LAMP) assay with neutral red, a pH-sensitive dye, as the color shift indicator. Neutral red exhibited a sharp contrast of color change from faint orange (negative) to pink (positive) during LAMP for detection of ASFV. The designed primer set targeting highly conserved region of the p72 gene was highly specific to ASFV and showed no cross-reactivity with other swine viruses. The detection limit for the one-step visual LAMP developed was 10 copies/reaction based on the recombinant plasmid containing the p72 gene of ASFV. More importantly, the developed one-step visual LAMP showed high consistency with the results of the real-time polymerase chain reaction (qPCR) method recommended by World Organization for Animal Health (OIE). Furthermore, the results demonstrate that the colorimetric detection with this LAMP assay could be directly applied for the whole blood and serum samples without requiring genome extraction. Based on our results, the developed one-step visual LAMP assay is a promising penside diagnostic tool for development of early and cost-effective ASF monitoring program that would greatly contribute to the prevention and control of ASF.
非洲猪瘟(ASF)给全球养猪业造成了巨大经济损失。由于尚无商业化的ASF疫苗,早期诊断对于预防和控制该疾病极为重要。在本研究中,选取了非洲猪瘟病毒(ASFV)衣壳蛋白编码基因(p72)并用于设计引物,以建立一种以pH敏感染料中性红作为颜色变化指示剂的一步可视化环介导等温扩增(LAMP)检测方法。在检测ASFV的LAMP反应过程中,中性红呈现出从浅橙色(阴性)到粉红色(阳性)的鲜明颜色变化对比。针对p72基因高度保守区域设计的引物组对ASFV具有高度特异性,与其他猪病毒无交叉反应。基于含有ASFV p72基因的重组质粒,所开发的一步可视化LAMP检测限为10拷贝/反应。更重要的是,所开发的一步可视化LAMP与世界动物卫生组织(OIE)推荐的实时聚合酶链反应(qPCR)方法的结果高度一致。此外,结果表明,这种LAMP检测的比色法检测可直接应用于全血和血清样本,无需进行基因组提取。基于我们的结果,所开发的一步可视化LAMP检测方法是一种有前景的现场诊断工具,可用于制定早期且经济高效的ASF监测计划,这将极大地有助于ASF的预防和控制。