A recombinant rabies virus carrying GFP between N and P affects viral transcription in vitro

• DOI: 10.1007/s11262-016-1313-2
• Publication Date: 2016-03-08T07:19:28Z
• Authors: Jun Luo; Jing Zhao; Qin Tian; Weiyu Mo; Yifei Wang; Hao Chen; Xiaofeng Guo
• Keywords: Transcription, Genetic; Genetic Vectors; Green Fluorescent Proteins; Genome, Viral; Article; Cell Line; Viral Proteins; 03 medical and health sciences; Virology; Cricetinae; Genetics; Animals; Molecular Biology; Viral Structural Proteins; Vaccines, Synthetic; 0303 health sciences; DNA-Directed RNA Polymerases; Nucleocapsid Proteins; Viral Load; Phosphoproteins; Immunity, Innate; 3. Good health; Rabies Vaccines; Rabies virus; RNA, Viral; Molecular Chaperones

Several studies have demonstrated the rabies virus to be a perfect potential vaccine vector to insert foreign genes into the target genome. For this study, a green fluorescent protein (GFP) gene was cloned into the rabies virus (RABV) genome between the N and P gene. CT dinucleotide was inserted as intergenic region. The recombinant high egg passage Flury strain (HEP-Flury) of RABV, carrying GFP (rHEP-NP-GFP), was generated in BHK-21 cells using reverse genetics. According to the viral growth kinetics assay, the addition of GFP between N and P gene has little effect on the viral growth compared to the parental strain HEP-Flury. Quantitative real-time PCR (qPCR) indicated that rHEP-NP-GFP showed different viral gene transcription, especially for G gene, compared to HEP-Flury. The same is true for one other recombinant RABV carrying GFP between G and L gene in NA cells. In addition, parent HEP-Flury showed more expression of innate immune-related molecules in NA cells. Compared to HEP-Flury, Western blotting (WB) indicated that insertion of a foreign gene following N gene enhanced the expression of M and G proteins. According to the qPCR and WB, GFP expression levels of rHEP-NP-GFP were significantly higher than rHEP-GFP. This study indicates HEP-Flury as valid vector to express exogenous genes between N and P.