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Open Access Research article

Generation of recombinant Orf virus using an enhanced green fluorescent protein reporter gene as a selectable marker

Zhangyong Ning12, Yongzheng Peng13, Wenbo Hao4, Chaohui Duan15, Daniel L Rock1 and Shuhong Luo14*

Author Affiliations

1 Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Champaign-Urbana, 2001 S. Lincoln Avenue, Urbana, IL 61802, USA

2 College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, People's Republic of China

3 Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, People's Republic of China

4 Institute of Antibody Engineering, School of Biotechnology, Southern Medical University, 1838 N. Guangzhou Avenue,Guangzhou, 510515, People's Republic of China

5 Laboratory of Clinical Immunology, the Sun Yat-Sen Memorial hospital, Sun Yat-Sen University, Guangzhou 510120, Guangdong, People's Republic of China

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BMC Veterinary Research 2011, 7:80  doi:10.1186/1746-6148-7-80

Published: 22 December 2011

Abstract

Background

Reporter genes are often used as a selectable marker for generation of recombinant viruses in order to investigate the mechanism of pathogenesis and to obtain candidate vaccine viruses. Routine selection of the recombinant parapoxvirus is time-consuming and labor intensive. Therefore, developing a novel method for selection is critical.

Results

In this study, we developed a rapid method to generate recombinant Orf viruses (ORFV) based on the enhanced green fluorescent protein (EGFP) reporter gene as a selectable marker. The coding sequence of EGFP gene was amplified from pEGFP-N1 vector and subcloned into the pZIPPY-neo/gus plasmid under the control of the early-late vaccinia virus (VACV) VV7.5 promoter and flanked by two multiple cloning sites (MCS) to generate a novel transfer vector pSPV-EGFP. Using the pSPV-EGFP, two recombination cassettes pSPV-113LF-EGFP-113RF and pSPV-116LF-EGFP-116RF were constructed by cloning the flanking regions of the ORFV113 and ORFV116 and inserted into two MCS flanking the EGFP gene. Using this novel system, two single gene deletion mutants OV-IA82Δ113 and OV-IA82Δ116 were successfully generated.

Conclusions

This approach shortens the time needed to generate recombinant ORFVs (rORFVs). Thus, the pSPV-EGFP vector provides a direct, fast, and convenient way to manipulate the recombinant viruses, indicating that it is highly suited for its designed purpose.