Key Projects in the National Science and Technology Pillar Program(No. 2006BAD06A17-08), Science and Technology Program of Heilongjiang Province(No. GA06B202), Earmarked Fund for Modern Agro-industry Technology Research System(No. nycytx-0303).
After sequencing the Asia 1 foot-and-mouth disease virus (FMDV) (As01 strain), we amplified the two fragments covering the whole genome by overlapping PCR and long PCR. The 5¢ fragment was 1.8 kb in length including 15Cs, and the 3¢ fragment was 6.7 kb in length. The two fragments were cloned into the pBluescript SK vector to construct recombinant plasmid pBSAs carrying the full-length cDNA of FMDV As01 strain. The RNA transcript was synthesized in vitro using T7 polymerase and transfected into BHK-21 cells. We observed the typical CPE caused by rescued FMDV. The harvested virus was confirmed to be Asia 1 FMDV by RT-PCR, indirect immunofluorescence assay (IFA) and electron microscope observation. The rescued virus showed a similar pathogenicity in suckling mouse (LD50) compared to its wild-type virus. The infectious cDNA clone of the FMDV As01 strain laid a new ground for further investigation of FMDV virulence determinants and development of novel vaccines against FMD.
李爽,张润祥,宋鸽,高明春,刘湘涛,王君伟. 牛Asia 1型口蹄疫病毒感染性克隆的构建[J]. Chinese Journal of Biotechnology, 2009, 25(11): 1621-1626
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