Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, College of Veterinary Medicine, Yangzhou University, Yangzhou, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety, the Ministry of Education of China, Yangzhou University, Yangzhou, China.
Transbound Emerg Dis. 2022 Sep;69(5):2971-2979. doi: 10.1111/tbed.14459. Epub 2022 Jan 28.
Genotype II African swine fever virus (ASFV) has been plaguing Chinese pig industry and caused severe morbidity and mortality of pigs resulting in huge economic losses since its first report in August 2018. Most recently, two genotype I ASFVs with low virulence but efficient transmissibility in pigs were reported in China, which makes the diagnosis and control of this lethal disease more challenging. Therefore, it is prerequisite and important to differentiate genotype I from genotype II upon ASFV outbreaks before making any stringent control procedures. In this study, a duplex real-time PCR assay based on ASFV E296R gene was established which could simultaneously detect genotypes I and II ASFVs with two pairs of primers and two probes. Plasmid containing ASFV genes was used to test the sensitivity, repeatability, and reproducibility. DNA or cDNA samples of ASFV and other swine viruses were used to test the specificity. The results showed that the established duplex real-time PCR assay has satisfied specificity, sensitivity, repeatability, and reproducibility. In addition, the assay was applied to differentiate 84 ASFV positive clinical samples including lymph nodes, spleen, kidney, lung, liver, blood, nasal swab, and environmental swab samples which were sent to National ASF Reference Laboratory from April 2020 to September 2021. The results showed that all these ASFV positive samples belong to genotype II ASFV. The established duplex real-time PCR in this study provides a powerful tool for rapid detection and differentiation between genotypes I and II ASFVs and will facilitate efficient control of ASFV in China.
自 2018 年 8 月首次报告以来,基因型 II 非洲猪瘟病毒(ASFV)一直困扰着中国的养猪业,导致猪的发病率和死亡率很高,造成了巨大的经济损失。最近,中国报告了两种毒力较低但在猪中传播效率较高的基因型 I ASFVs,这使得这种致命疾病的诊断和控制更加具有挑战性。因此,在实施任何严格的控制措施之前,对 ASFV 暴发进行基因型 I 和 II 的区分是必要的和重要的。在本研究中,建立了一种基于 ASFV E296R 基因的双重实时 PCR 检测方法,该方法可以使用两对引物和两个探针同时检测基因型 I 和 II ASFV。使用含有 ASFV 基因的质粒来测试灵敏度、重复性和重现性。使用 ASFV 和其他猪病毒的 DNA 或 cDNA 样本来测试特异性。结果表明,建立的双重实时 PCR 检测方法具有良好的特异性、灵敏度、重复性和重现性。此外,该检测方法还用于区分 2020 年 4 月至 2021 年 9 月期间国家 ASF 参考实验室收到的 84 份来自淋巴结、脾脏、肾脏、肺脏、肝脏、血液、鼻拭子和环境拭子的临床 ASFV 阳性样本。结果表明,所有这些 ASFV 阳性样本均属于基因型 II ASFV。本研究建立的双重实时 PCR 为快速检测和区分基因型 I 和 II ASFV 提供了有力工具,将有助于在中国有效控制 ASFV。