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基于结构蛋白基因 D117L 的 CRISPR/LwCas13a 侧向流条带可视化检测非洲猪瘟病毒的研究进展。

Development of visual detection of African swine fever virus using CRISPR/LwCas13a lateral flow strip based on structural protein gene D117L.

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety, Yangzhou 225009, PR China; Comparative Medicine Research Institute, Yangzhou University, Yangzhou, 225009, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, 225009, PR China.

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, PR China; Joint International Research Laboratory of Agriculture and Agri-Product Safety, Yangzhou 225009, PR China; Comparative Medicine Research Institute, Yangzhou University, Yangzhou, 225009, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, 225009, PR China.

出版信息

Vet Microbiol. 2024 Jun;293:110073. doi: 10.1016/j.vetmic.2024.110073. Epub 2024 Apr 3.

Abstract

African swine fever virus (ASFV) is a large double stranded DNA arbovirus that is highly contagious and seriously endangers domestic and wild pigs. In the past decade, African swine fever (ASF) has spread in many countries in the Caucasus, Russian Federation, Eastern Europe and Asia, causing significant losses to the pig industry. At present, there is a lack of effective vaccine and treatment for ASF. Therefore, the rapid and accurate detection is crucial for ASF prevention and control. In this study, we have developed a portable lateral flow strip (LFS) detection mediated by recombinase polymerase amplification (RPA) and CRISPR/LwCas13a, which is performed at 37 ℃ and visualized by eyes without the need for complex instruments. This RPA-LwCas13a-LFS is based on the ASFV structural protein p17 gene (D117L), with a detection sensitivity up to 2 gene copies. This method is highly specific and has no cross reactivity to 7 other pig viruses. In the detection of two batches of 100 clinical samples, the p17 (D117L) RPA-LwCas13a-LFS had 100% coincidence with conventional quantitative PCR (qPCR). These findings demonstrate the potential of this simple, rapid, sensitive, and specific ASFV detection method for on-site ASFV detection.

摘要

非洲猪瘟病毒(ASFV)是一种大型双链 DNA 虫媒病毒,具有高度传染性,严重危害家猪和野猪。在过去十年中,非洲猪瘟(ASF)在高加索、俄罗斯联邦、东欧和亚洲的许多国家传播,给养猪业造成了重大损失。目前,ASF 缺乏有效的疫苗和治疗方法。因此,快速准确的检测对于 ASF 的防控至关重要。本研究开发了一种基于重组酶聚合酶扩增(RPA)和 CRISPR/LwCas13a 的便携式侧向流动条(LFS)检测方法,该方法在 37℃下进行,可通过肉眼进行可视化,无需复杂仪器。该 RPA-LwCas13a-LFS 基于 ASFV 结构蛋白 p17 基因(D117L),检测灵敏度高达 2 个基因拷贝。该方法具有高度特异性,与其他 7 种猪病毒无交叉反应。在对两批 100 份临床样本的检测中,p17(D117L)RPA-LwCas13a-LFS 与常规定量 PCR(qPCR)的符合率为 100%。这些发现表明,这种简单、快速、灵敏、特异的 ASF 检测方法具有现场 ASF 检测的潜力。

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