Entire 3ABC sequence of FMDV containing a 6×his tag coding sequence at the N-terminal was obtained through PCR amplification using a pair of specific primers, subcloned into shuttle plasmid of pMelBac-B with a melittin secretion signal sequence and finally constructed recombinant plasmid of pMel-3ABC. After co-transfected the recombinant plasmid and linearized Bac-N-BlueTM DNA into Sf9 insect cell under intermediary agent of the Cellfectin?, the result showed that we have already acquired recombinant baculovirus by screen of plaque assay and identification of PCR. Though the recombinant baculovirus infecting the Sf9 cells again, experiments indicated that 3ABC gene could express in insect cells and the expressed protein was secreted in the supernatant of Sf9 cell culture possessing favourable biological activities detected by adopting two methods of SDS-PAGE and Western blot. The result verified that the protein could respond with sera derived from FMDV infected animals, but have no responsibility with sera derived from health animals and vaccinated animals detected by indirect ELISA using antigen of expressed protein after purification with Ni-NTA his bind resin. Therefore, this study has established a solid foundation for establishing an effective diagnosis method to discriminating the FMDV infected animals from vaccinated animals.
马江涛,卢曾军,曹轶梅,郭慧琛,郭建宏,祝秀梅,杨孝朴,刘在新. 口蹄疫病毒NSP 3ABC基因在昆虫细胞中的分泌表达及其活性检测[J]. Chinese Journal of Biotechnology, 2007, 23(3):
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