Abstract
Senecavirus A (SVA) is an emerging virus that causes vesicular disease in pigs. Construction of a full-length SVA cDNA clone is crucial for understanding its replication and pathogenesis. Here, we successfully constructed a CMV-promoter-driven infectious cDNA clone of the SVA isolate SVA/GX/CH/2018, which we named rSVA GX01. Sequence comparison between the pSVA GX01 and the parental isolate (SVA/GX/CH/2018) revealed three single-nucleotide differences. Four-week-old piglets were experimentally infected with either the parental virus or the cloned virus. The results showed that the cloned rSVA GX01 displayed weak pathogenicity in 4-week-old pigs compared to the parental virus SVA CH-GX-01-2018. The infectious clone of SVA will serve as a valuable tool for studying the viral replication cycle and for functional analysis of the viral genome.
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The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
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Acknowledgements
We are grateful to Dr. Dev Sooranna of Imperial College London for English language editing of the manuscript.
Funding
The Natural Science Foundation of China (31972666) and the Natural Science Foundation of Guangxi Province (No. 2018GXNSFDA281021) funded this research.
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Hao Wang: project administration, writing – original draft. Yongfang Mo: conceptualization. Wenbo Liu: funding acquisition. Chenxia Niu: software. Qijie He: investigation. Tongwei Ren: methodology. Kang Ouyang: resources. Ying Chen: software. Weijian Huang: validation. Zuzhang Wei: visualization, writing – review & editing. All of the authors reviewed the manuscript.
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The animal experiments were approved by the Animal Experiment Committee of Guangxi University, with the approval number (GXU2022-266).
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Wang, H., Mo, Y., Liu, W. et al. Construction and characterization of a full-length infectious clone of an emerging senecavirus A strain. Arch Virol 169, 25 (2024). https://doi.org/10.1007/s00705-023-05951-y
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DOI: https://doi.org/10.1007/s00705-023-05951-y