Zhu Pei, Li Zhanhong, Li Zhuoran, Meng Li, Liu Peng, Sun Xiutao, Yang Qi, Song Jianling
Yunnan Tropical and Subtropical Animal Virus Diseases Laboratory, Yunnan Animal Science and Veterinary Institute, Kunming 650224, China.
Key Laboratory of Transboundary Animal Diseases Prevention and Control (Co-Construction by Ministry and Province), Yunnan Animal Science and Veterinary Institute, Kunming 650224, China.
Viruses. 2025 Mar 31;17(4):505. doi: 10.3390/v17040505.
In order to investigate the causes of swine diarrhea in Yunnan Province, this study was conducted to detect and monitor diarrhea viruses through regular sampling and reverse transcription polymerase chain reaction (RT-PCR). In October 2023, porcine sapelovirus (PSV) was detected in fecal specimens collected from diarrheal pigs in Honghe City, and three strains of PSV were successfully isolated by inoculating them into PK-15 cells; electron microscopy revealed virus particles with diameters of ~32 nm. Next-generation sequencing (NGS) revealed that the PSV isolate genomes ranged from 7480 to 7515 nucleotides in length. Homology analyses indicated that ML-15 and ML-16 showed the highest nucleotide and amino acid identities with the Asian PSV strains, ML-19 showed the highest sequence identities with the Zambia PSV strains, and the VP1 to VP4 genes of the three PSV isolates were in the hypervariable region. Phylogenetic analyses showed that the three PSVs isolated in this study all clustered together with Chinese PSV strains; furthermore, recombination analyses indicated that PSV-ML-19 might be a recombined strain and may have emerged through genetic recombination between the major putative parent strain PSV-21-V and the minor putative parent GER L00798-K11 14-02. This was the first reported instance of the isolation and phylogenetic analyses of the PSV strains in Yunnan Province, which enriched the understanding of Chinese PSV strains and indicated the need to prevent and control PSV; the mutation of the VP1 and 3D genes may also provide an important reference for the development of PSV vaccines.
为调查云南省猪腹泻的病因,本研究通过定期采样和逆转录聚合酶链反应(RT-PCR)对腹泻病毒进行检测和监测。2023年10月,在从红河州腹泻猪采集的粪便标本中检测到猪萨佩罗病毒(PSV),通过将其接种到PK-15细胞中成功分离出3株PSV;电子显微镜显示病毒粒子直径约为32 nm。二代测序(NGS)显示,PSV分离株基因组长度在7480至7515个核苷酸之间。同源性分析表明,ML-15和ML-16与亚洲PSV毒株的核苷酸和氨基酸同一性最高,ML-19与赞比亚PSV毒株的序列同一性最高,3株PSV分离株的VP1至VP4基因位于高变区。系统发育分析表明,本研究分离的3株PSV均与中国PSV毒株聚集在一起;此外,重组分析表明,PSV-ML-19可能是一个重组毒株,可能是通过主要推定亲本毒株PSV-21-V和次要推定亲本GER L00798-K11 14-02之间的基因重组产生的。这是云南省首次报道PSV毒株的分离和系统发育分析,丰富了对中国PSV毒株的认识,表明需要对PSV进行防控;VP1和3D基因的突变也可能为PSV疫苗的研发提供重要参考。
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