Abstract
Canine parvovirus (CPV) is an important and highly prevalent pathogen of dogs that causes acute hemorrhagic enteritis disease. Here, we describe a rapid method for the construction and characterization of a full-length infectious clone (rCPV) of CPV. Feline kidney (F81) cells were transfected with rCPV incorporating an engineered EcoR I site that served as a genetic marker. The rescued virus was indistinguishable from that of wild-type virus in its biological properties.
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Acknowledgements
This work was supported by 863 Project (2011AA10A213) and National Key Research and Development Program of China (2016YFD0501001).
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Conceived and designed the experiments: Yongle Yu and Weiquan Liu. Performed the experiments: Yongle Yu. Analyzed the data: Yongle Yu. Contributed reagents/materials/analysis tools: Yongle Yu, Jun Su, Jigui Wang, Ji Xi, Yaping Mao, Qiang Hou, Xiaomei Zhang, and Weiquan Liu. Wrote the paper: Yongle Yu and Weiquan Liu.
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No conflict of interest exists in the submission of this manuscript, and manuscript is approved by all authors for publication.
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All animal experiments were performed following protocols approved by the State Key Laboratory of Agrobiotechnology Animal Study Proposal of China Agricultural University.
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Edited by Zhen F. Fu.
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Yu, Y., Su, J., Wang, J. et al. A rapid method for establishment of a reverse genetics system for canine parvovirus. Virus Genes 53, 876–882 (2017). https://doi.org/10.1007/s11262-017-1497-0
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DOI: https://doi.org/10.1007/s11262-017-1497-0