Heilongjiang Provincial Key Laboratory of Laboratory Animal and Comparative Medicine, State Key Laboratory of Veterinary Biotechnology, National Poultry Laboratory Animal Resource Center, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
Laboratory of Inspection and Testing, Hebei Provincial Station of Veterinary Drug and Feed, Shijiazhuang 050000, China.
Viruses. 2022 Feb 8;14(2):349. doi: 10.3390/v14020349.
Porcine sapelovirus (PSV) is an important emerging pathogen associated with a wide variety of diseases in swine, including acute diarrhoea, respiratory distress, skin lesions, severe neurological disorders, and reproductive failure. Although PSV is widespread, serological assays for field-based epidemiological studies are not yet available. Here, four PSV strains were recovered from diarrheic piglets, and electron microscopy revealed virus particles with a diameter of ~32 nm. Analysis of the entire genome sequence revealed that the genomes of PSV isolates ranged 7569-7572 nucleotides in length. Phylogenetic analysis showed that the isolated viruses were classified together with strains from China. Additionally, monoclonal antibodies for the recombinant PSV-VP1 protein were developed to specifically detect PSV infection in cells, and we demonstrated that isolated PSVs could only replicate in cells of porcine origin. Using recombinant PSV-VP1 protein as the coating antigen, we developed an indirect ELISA for the first time for the detection of PSV antibodies in serum. A total of 516 swine serum samples were tested, and PSV positive rate was 79.3%. The virus isolates, monoclonal antibodies and indirect ELISA developed would be useful for further understanding the pathophysiology of PSV, developing new diagnostic assays, and investigating the epidemiology of the PSV.
猪传染性胃肠炎病毒(PSV)是一种重要的新兴病原体,与猪的多种疾病有关,包括急性腹泻、呼吸窘迫、皮肤损伤、严重的神经紊乱和繁殖失败。尽管 PSV 广泛存在,但目前还没有用于现场流行病学研究的血清学检测方法。在这里,从腹泻仔猪中分离到了 4 株 PSV,电镜显示病毒粒子的直径约为 32nm。对整个基因组序列的分析表明,PSV 分离株的基因组长度为 7569-7572 个核苷酸。系统进化分析表明,分离的病毒与来自中国的毒株归为一类。此外,还制备了针对重组 PSV-VP1 蛋白的单克隆抗体,用于特异性检测细胞中的 PSV 感染,我们证明分离的 PSV 只能在猪源细胞中复制。我们首次使用重组 PSV-VP1 蛋白作为包被抗原,建立了用于检测血清中 PSV 抗体的间接 ELISA。共检测了 516 份猪血清样本,PSV 的阳性率为 79.3%。这些病毒分离株、单克隆抗体和间接 ELISA 将有助于进一步了解 PSV 的病理生理学,开发新的诊断方法,并研究 PSV 的流行病学。