- Open Access
Generation of a recombinant rabies Flury LEP virus carrying an additional G gene creates an improved seed virus for inactivated vaccine production
© Tao et al; licensee BioMed Central Ltd. 2011
Received: 16 May 2011
Accepted: 25 September 2011
Published: 25 September 2011
The rabies Flury Low Egg Passage virus (LEP) has been widely used as a seed virus to generate inactive vaccine. Here, we established a reverse genetic system for LEP and generated a recombinant LEP virus (rLEP-G) that carries two identical G genes. This recombinant virus showed similar properties to those of LEP with respect to in vitro growth, neurotropism index, and virulence in mice. rLEP-G produced 4.3-fold more G protein than did LEP in BHK-21 cells. The inactivated vaccine generated from rLEP-G induced significantly higher virus neutralization titers in mice and dogs than those produced in response to LEP-derived vaccine. Our results suggest that rLEP-G is an improved seed virus candidate for inactivated rabies virus vaccine manufacture.
Rabies virus (RV) belongs to the genus Lyssavirus of the family Rhabdoviridae, and causes a fatal neurological disease in humans and animals  More than 55,000 people die of rabies each year, and about 95% of these deaths occur in Asia and Africa . An estimated 31,000 people die from dog rabies in Asia each year, with most cases occurring in India and China [3, 4]. The most cost-effective strategy for preventing rabies in people is to eliminate rabies in dogs via vaccination [5–7]Inactivated rabies vaccine has been shown to be a safe and efficient means to control rabies in dogs. However, the vaccination rate of dogs in many developing countries is low, especially in rural areas, mainly due to low economic development and the high cost of vaccination More efficient and lower cost inactivated vaccine is, therefore, still needed.
The surface glycoprotein (G) of RV is the major antigen responsible for the induction of protective immunity  Increasing G protein levels should, therefore, enhance the protective viral neutralization antibody (VNA) response. The rabies Flury low egg passage virus (LEP) has been widely used as a seed virus to generate inactive vaccine for humans and animals because of its high immunogenicity and high growth titer in cell culture . Here, we generated a recombinant LEP virus that carries two identical G genes to increase G protein expression. Growth curves, neurotropism index, virulence, and the G protein expression level of the double-G LEP were tested in vitro and in vivo. The immunogenicity of the inactivated vaccine derived from this double-G LEP was also evaluated in mice and dogs and compared with that of LEP.
Materials and Methods
Viruses and cells
Neuroblastoma (NA) cells of A/J mouse origin were grown in Eagle's minimum essential medium (MEM) supplemented with 10% fetal bovine serum (FBS). Baby hamster kidney (BHK-21) cells were grown in Dulbecco's modified Eagle's MEM (DMEM) supplemented with 10% FBS. The RV LEP (AV2012) was obtained from the China Veterinary Culture Collection Center and propagated in BHK-21 cells. A street virus, GX/09, was isolated from the brain of a dog that died of rabies and was propagated in the brain of adult mice. All viruses were kept in at -70°C before use.
Primers used to construct the full-length cDNA clone and helper plasmids for Flury LEP
For F1 amplification
TGCGCTAGC TGTTAAGCGTCTGATGAGTCCGTGAGGACGAAACTATAGGAAAGGAATTCCTATAGTC ACGCTTAACAACAAAACCAAAGAAb
For F2 amplification
For F3 amplification
For Pme I mutation
GACTTGAAGTT TA AAC AGGATGACCGGCCd
GGCCGGTCATCCTG TTT AA ACTTCAAGTC
For G gene amplification
For N gene amplification
For L gene amplification
For LEP-G confirmation
BHK-21 cells were grown overnight to 80% confluence in 6-well plates in DMEM supplemented with 10% FBS. Cells were transfected with 4.0 μg of the full-length plasmid pLEP-G, 2 μg of pCA-N, 1 μg of pCA-P, and 1 μg of pCA-L by using Lipofectamine™ 2000 (Invitrogen) according to the manufacturer's protocol. After 4-6 h, the transfection medium was replaced with fresh medium. After 3 days, supernatants were transferred onto BHK-21cells and incubated for a further 3 days. Rescued viruses were examined by using an indirect fluorescence assay (IFA) with mouse anti-RV serum and FITC-conjugated goat anti-mouse IgG (Sigma). Supernatants from virus-positive cultures were collected to propagate virus stocks in BHK-21 cells. Sequences of recovered viruses were confirmed by sequencing entire viral genomes. To confirm whether the recovered rabies virus was derived from the cloned pLEP-G, RT-PCR was performed with the primers shown in Table 1, positive-sense G4 and negative-sense G3 primers at nucleotide positions 4,302 to 4,321 and 3,613 to 3,632 (based on the genomic nucleotide number of the LEP strain), respectively. The fragment was further digested with Pme I, and the supernatants from virus-positive cultures were used to produce virus stocks in BHK-21 cells. The rescued virus generated from the full-length plasmid pLEP-G was designated as rLEP-G.
Multistep growth assays
Confluent BHK-21 or NA cell monolayers grown in 6-well plates were infected with LEP or rLEP-G at a multiplicity of infection (MOI) of 0.01. After incubation for 1 h at 37°C, the inoculums were removed and the cells were washed twice with PBS. BHK-21 and NA cells were replenished with DMEM containing 2% FBS or with MEM containing 0.2% FBS, respectively, and incubated at 37°C. Culture supernatant (100 μl) was harvested at 0, 1, 2, 3, 4, and 5 days post-inoculation for virus titration.
Monolayers of NA or BHK-21 cells in 24-well plates were infected with 10-fold dilutions of virus suspension and incubated at 37°C. At 48 h post-infection, an IFA test was performed. Foci were counted under a fluorescence microscope and calculated as focus forming unit/ml (FFU/ml).
The in vitro neurotropism index was expressed as the logarithm of the titer of virus stock in NA cells minus the logarithm of the titer of the same stock in BHK-21 cells . The virus titers for neurotropism index calculation were based on the titration results of virus stock harvested at 72 h post infection.
BHK-21 cells grown in 6-well plates were infected with LEP or rLEP-G at an MOI of 1 and incubated for 48 h. G gene expression was confirmed by using western blotting as described previously . Briefly, cell extracts were subjected to 10% polyacrylamide gel electrophoresis (SDS-PAGE), and then blotted to nitrocellulose membrane. The membrane was incubated with a mixture of mouse anti-G protein polyclonal antiserum and anti-β-actin monoclonal antibody (Santa Cruz Biotechnology), as the first antibody, and then with IRDye700-conjugated anti-mouse IgG (Rockland, Gilbertsville, PA) as the second antibody. The mouse anti-G protein polyclonal antiserum was generated by immunization with a recombinant Newcastle disease virus that expresses the RV glycoprotein and was developed in our lab. Signal intensities were analyzed by using the Odyssey infrared image system (LiCor). The densitometry of each band was quantified with Photoshop CS2. The G/β-actin ratio was calculated by dividing the densitometry of the G protein band by that of the β-actin protein band.
Infection of mice
The virulence of LEP and rLEP-G for adult mice was measured in 6-week-old female Balb/c mice (Vital River, Beijing). To determine the 50% lethal dose (LD50) of each virus, groups of five adult mice were inoculated intracerebrally (i.c.) with 30 μl or intramuscularly (i.m.) with 100 μl of serial 10-fold dilutions of LEP or rLEP-G. After infection, mice were observed for 21 days for clinical signs or death. The LD50 of each virus was calculated by using the method of Reed and Muench .
Preparation of inactivated vaccines
BHK-21 cells grown in 75 cm2 flask were infected with LEP or rLEP-G at an MOI of 0.01 and incubated at 37°C. At 96 h post-infection, cells were suspended in the supernatant by using a rubber policeman. The suspension was submitted to three cycles of freezing and thawing (-20°C/37°C, 5 min each) and then subjected to ultrasonic sound to increase the cell extraction dissolution. After centrifuge, supernatants were collected and stored in -70°C. The infectious viruses in the supernatant were titrated in BHK cells. To prepare inactivated vaccines, the supernatant was incubated at 37°C for 2 h in the presence of 0.03% β-propiolactone. Then, three volumes of inactivated supernatant preparation (non-dilution, 20-f old dilution, and 80-fold dilution) were mixed with one volume of Rehydraphos AlPO4 adjuvant (Reheis, Berkeley Heights, NJ), and stored at 4°C for vaccination.
Immunization of Balb/c mice and dogs
Groups of ten 4-week-old female Balb/c mice were inoculated i.m. in the gastrocnemius muscle with 100 μl of 20- or 80-fold dilutions of inactivated vaccine preparations. Groups of six 3-month-old Beagles were inoculated i.m. with 1 ml of inactivated vaccine preparations.
Three weeks after immunization, mice were bled from the retro-orbital sinus under isoflurane inhalation anesthesia and Beagles were bled from the vein of the front leg. Sera were tested for neutralizing antibodies (VNA) by using the rapid fluorescent focus inhibition test (RFFIT) . Neutralization titers, defined as the highest serum dilution that neutralizes 50% of the challenge virus, were normalized to international units (IU) according to the World Health Organization anti-RV antibody standard.
Recovery of rLEP-G from cloned cDNA
Growth properties of rLEP-G in vitro
Pathogenicity of rLEP-G in adult mice
Induction of VNA in mice and dogs
Mass vaccination of dogs has proven to be an effective way to control rabies in this species. However, current live attenuated vaccines can have safety issues [14, 15], and the use of current inactivated vaccines is limited in developing countries because of high manufacturing costs. Increasing G protein expression in RV seed viruses is hypothesized to improve rabies inactivated vaccines not only via immunogenicity but also through increased manufacturing productivity. Previous studies have demonstrated the feasibility of introducing an additional G gene into the RV genome [16–18]. By using reverse genetics technology, Faber et al. generated a double-G gene recombinant RV (SPBNGA-GA). This double-G virus showed a 1.6-fold increase in G protein expression in cell culture relative to that of its single-G gene parent virus (SPBNGA). Inoculation with SPBNGA-GA live virus provided more efficient protective immunity than did the SPBNGA strain in mice. However, the utility of SPBNGA-GA as a seed virus for inactivated vaccine production has not been evaluated further . In another study, Hosokawa-Muto et al. generated a double-G gene recombinant RV RC-HL. This virus showed a 1.5-fold increase in G protein expression in cell culture compared with that induced in the single-G gene parent virus RC-HL. When the recombinant double-G gene RC-HL and wild-type RC-HL were inactivated and used to vaccinated mice, no significant difference in RV neutralization antibody responses was observed.
Here, we generated a recombinant LEP virus carrying an additional G gene, rLEP-G. This recombinant virus produced strikingly higher levels of G protein in cell culture and showed similar in vitro growth properties and bio-safety characteristics. Inactivated vaccine prepared from rLEP-G induced significant higher RV VNA titers in mice and dogs than those induced by LEP-derived vaccine, indicating that rLEP-G represents an improved seed virus candidate for inactivated RV vaccine manufacture.
Since G protein is a major contributor to the pathogenicity of rabies virus [19–22], we evaluated whether this increase in G protein expression affected the virulence of the rLEP-G virus. We found that the insertion of this additional G gene results in increase of G protein expression but not in increase of the neuro-invasiveness or peripheral pathogenicity of the virus in adult mice. In other studies, introduction of one or two additional G genes into the genome of rabies virus resulted in a higher level of G protein expression and attenuate pathogenicity in adult mice [17, 18, 23]. As the pathogenicity of a particular RV strain correlates inversely with its ability to trigger apoptosis in neuron cells, one possible explanation for this discrepancy is that some lethal viruses, such as LEP and rLEP-G, rarely induced apoptosis in neuron cells. In fact, our previous data had shown that there was no clear correlation between apoptosis induction and the viral replication titers or glycoprotein expression level among LEP and its relative mutants or chimerical viruses.
We thank Susan Watson for editing the manuscript. This work was supported by Chinese National S&T Plan (2009ZX10004-214), by the grant from Chinese Ministry of Agriculture (200803014) and by the GHI program of Emory University.
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