Abstract
In this study, we describe a novel and rapid method for the construction of a full-length infectious clone (pPPV). The constructed clone contained an engineered EcoRv site that served as a genetic marker and was shown to be infectious when transfected into a monolayer of PK-15 cells. The rescued virus (rPPV) of the infectious clone was found to be indistinguishable from wild-type virus BQ in terms of its biological properties. The generation of this PPV infectious clone provides a potentially powerful tool with which to elucidate the molecular pathogenesis of PPV.
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Acknowledgements
This work was supported by the Agricultural Science and Technology Innovation Program (ASTIP-IAS15), National Natural Science Foundation of China (NO. 31172349 & NO. 31172341) and the National Key Research and Development Program of China (No. 2016YFD0501003 & 2017YFD0502300).
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Zhang, L., Gao, D., Yu, Y. et al. Establishment of a rescue system for porcine parvovirus using a seamless cloning method. Arch Virol 164, 1459–1467 (2019). https://doi.org/10.1007/s00705-019-04209-w
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DOI: https://doi.org/10.1007/s00705-019-04209-w