Lu Shuhan, Li Fang, Chen Qiubing, Wu Jing, Duan Junyi, Lei Xinlin, Zhang Ying, Zhao Dongming, Bu Zhigao, Yin Hao
Department of Pathology, Frontier Science Center for Immunology and Metabolism, Medical Research Institute, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
2State Key Laboratory of Veterinary Biotechnology, National High Containment Laboratory for Animal Diseases Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Cell Discov. 2020 Apr 7;6:18. doi: 10.1038/s41421-020-0151-5. eCollection 2020.
African swine fever virus (ASFV) is a dsDNA virus responsible for a severe, highly contagious, and lethal disease affecting both domestic and wild pigs. ASFV has brought enormous economic loss to a number of countries, and effective vaccine and therapy are still lacking. Therefore, a rapid, sensitive, and field-deployable detection of ASFV is important for disease surveillance and control. Herein, we developed a Cas12a-mediated portable paper assay to rapidly and precisely detect ASFV. We identified a robust set of crRNAs that recognized the highly conserved region of essential ASFV genes. The Cas12a-mediated detection assay showed low tolerance for mismatch mutations, and no cross-reactivity against other common swine pathogens. We further developed a paper-based assay to allow instrument-free detection of ASFV. Specifically, we applied gold nanoparticle-antibody conjugate to engineer homemade strips and combined it with Cas12a-mediated ASFV detection. This portable paper, instrument-free diagnostics, faithfully detected ASFV in swine samples, showing comparable sensitivity to the traditionally instrument-dependent qPCR method. Taking together, we developed a highly sensitive, instant, and economic Cas12a-mediated paper diagnostics of ASFV, with a great application potential for monitoring ASFV in the field.
非洲猪瘟病毒(ASFV)是一种双链DNA病毒,可引发一种严重、高度传染性且致命的疾病,影响家猪和野猪。ASFV给许多国家带来了巨大的经济损失,目前仍缺乏有效的疫苗和治疗方法。因此,快速、灵敏且可在现场部署的ASFV检测对于疾病监测和控制至关重要。在此,我们开发了一种基于Cas12a的便携式试纸检测法,用于快速、准确地检测ASFV。我们鉴定出了一组强大的crRNA,它们可识别ASFV必需基因的高度保守区域。Cas12a介导的检测法对错配突变耐受性低,且对其他常见猪病原体无交叉反应。我们进一步开发了一种基于试纸的检测法,可实现对ASFV的无需仪器检测。具体而言,我们应用金纳米颗粒-抗体偶联物制作自制试纸条,并将其与Cas12a介导的ASFV检测相结合。这种便携式、无需仪器的诊断方法能够准确检测猪样本中的ASFV,其灵敏度与传统的依赖仪器的qPCR方法相当。综上所述,我们开发了一种高度灵敏、即时且经济的基于Cas12a的ASFV试纸诊断方法,在现场监测ASFV方面具有巨大的应用潜力。