Cloning, expression and characterization of gE protein of Duck plague virus
- Hua Chang†1,
- Anchun Cheng†1, 2, 3Email author,
- Mingshu Wang†1, 2,
- Dekang Zhu†1, 2,
- Renyong Jia†2,
- Fei Liu2,
- Zhengli Chen2,
- Qihui Luo2,
- Xiaoyue Chen1, 2, 3 and
- Yi Zhou2
© Chang et al; licensee BioMed Central Ltd. 2010
Received: 16 March 2010
Accepted: 8 June 2010
Published: 8 June 2010
The gE protein of duck plague virus is the important membrane glycoprotein, its protein characterization has not been reported. In this study, we expressed and presented the characterization of the DPV gE product.
According to the sequence of the gE gene, a pair of primers were designed, and the DNA product with 1490bp in size was amplified by using the polymerase chain reaction (PCR). The PCR product was cloned into pMD18-T vector, and subcloned into pET32a(+), generating the recombinant plasmid pET32a/DPV-gE. SDS-PAGE analysis showed that the fusion pET32a/DPV-gE protein was highly expressed after induction by 0.2 mM IPTG at 30°C for 4.5 h in Rosseta host cells. Over expressed 6×His-gE fusion protein was purified by nickel affinity chromatography, and used to immunize the rabbits for the preparation of polyclonal antibody. The result of the intracellular localization revealed that the gE protein was appeared to be in the cytoplasm region. The real time PCR, RT-PCR analysis and Western blotting revealed that the gE gene was produced most abundantly during the late phase of replication in DPV-infected cells.
In this work, the DPV gE protein was successfully expressed in a prokaryotic expression system, and we presented the basic properties of the DPV gE product for the first time. These properties of the gE protein provided a prerequisite for further functional analysis of this gene.
Duck plague (DP), which is caused by DPV, is an acute, febrile, contagious, and septic disease of waterfowl (ducks, geese, and swans) . DPV has been classified as belonging to the Alphaherpesvirinae subfamily of the family Herpesviridae on the basis of the report of the Eighth International Committee on Taxonomy of Viruses (ICTV), but it has not been grouped into any genus . The genome of DPV, a linear and double stranded DNA, is about 150 kb. Recently, an increasing number of DPV genes, such as UL5 , UL6 , UL22, UL23(TK) , UL24 [5, 6], UL25, UL26, UL26.5, UL27, UL28, UL29, UL30 , UL31 [8, 9], UL32, UL33, UL34 , UL35 [8, 11], UL44 (gC) , UL50 , UL51 , US8 , US2 and US10  have been identified. Some genes were not essential for replication of the virus in cell culture in Herpesviridae, these dispensable gene products were, however, thought to be important for virus growth and spread in the natural host . The envelope glycoprotein E (gE) in Herpesviridae was important for the expression of virulence of the virus. It was necessary that the virus transfered in olfactory, trigeminal, sympathetic, and parasympathetic pathways [17, 18], and played an important role in cell-to-cell spread, though it was not a essential protein for in vitro replication [19–21]. In addition, the gE protein, an important envelope glycoprotein, was present in almost all examined the field isolates, and the gE antigen was used in the serological diagnosis, which was detected the antibodies against gE in the natural infection .
In 2006, a DPV genomic library was successfully constructed in our laboratory . Sequence analysis showed that the gE gene of DPV was predicted to encode a 490 amino acid protein with a molecular mass of 54 kDa . The report focused on the product of the DPV gE gene. We constructed the recombinant expression vector pET32a/DPV-gE, the fusion pET32a/DPV-gE protein (approximately 74 kDa) was expressed by the addition of isopropyl-β-D-thiogalactopyranoside (IPTG). The recombinant gE protein was purified and used to immunize the rabbits for the preparation of polyclonal antibody. We examined further the intracellular localization of the gE protein using the rabbit polyclonal antiserum specific to it in DPV-infected cells. We examined the expression of gE protein in DPV-infected cells using Western blotting, and analyzed the DPV gE gene transcription in DPV-infected cells using the real time PCR and RT-PCR.
Cloning of DPV gE gene and the correct recombinant plasmid
Expression and purification of the gE recombinant protein
The immunogenicity of the recombinant protein gE was tested with the anti-DPV polyclonal IgG as the first antibody by western blotting analysis. The result indicated a single band at apparent molecular mass of 74 kDa region was obtained with the recombinant plasmid pET32a/DPV-gE in E. coli Rosseta, which was induced by IPTG (Fig 3B, Lane 2). However, the band was not detected without induction. (Fig 3B, Lane 1). And the recombinant protein gE was recognized with the pET32a/DPV-gE antiserum as the first antibody by western blotting analysis. The result showed a specific signal at about 74 kDa (Fig 3C, Lane 3), no positive signal was detected without induction (Fig 3C, Lane 4) and observed when using the pre-immune serum (Fig 3C, Lane 5).
Dynamic proliferation of gE expression in DPV-infected cells
Intracellular localization of the gE product in DPV-infected cells
Transcription analysis of the gE gene in DPV-infected cells
DPV gE is a typical membrane glycoprotein which spanned 490 amino acids. Computer analysis showed there were six putative N-glycosylation sites in DPV gE epitopes and there was an immunodominant region consisting of twenty-one distinct, conformation-dependent epitopes in DPV gE . In this report, as the first step towards studying the properties and function of the gE protein. The PCR product of the gE was inserted into the vector pMD18-T, the recombinant plasmid pMD18/DPV-gE was confirmed by restriction digestion and DNA sequencing. The sequencing result showed that there were no nucleotide errors in the synthetic gE gene. This recombinant plasmid pMD18/DPV-gE could be used for further experiments to study the gE gene product.
We choosed the protocaryon expression vectors pET32a(+), which featured a high stringency T7 lac promoter, 6×His-tag, and thioredoxin, had been recognized as one of the most powerful tools for producing the recombinant proteins in E. coli . The thioredoxin could not only reduce the digestion by bacterial proteases, but also promote the expression of the recombinant fusion protein . The correct recombinant plasmid pMD18/DPV-gE was digested with EcoRI and XhoI, and the gE gene was directionally inserted in-frame downstream of the region encoding six histidine residues in the Escherichia coil expression vector pET32a(+). Expression of this fusion pET32a/DPV-gE protein is regulated by an IPTG-inducible lac operator and translation is expected to terminate at the stop codon of the gE gene. To obtain the highly expressed level of the fusion pET32a/DPV-gE protein as possible, the recombinant expression was transformed into E.coli BL21(pLysS), BL21(DE3) and Rosseta host cells, and optimized the condition for induction. Although there was 62 rare codons and 8 consecutive rare codons in gE ORF, which may influence the expression of the gE in vitro , the host bacteria Rosseta should impove the expression of the exogenous gene. The different temperatures, different IPTG concentrations, and different incubation times could effect the expressed level of the pET32a/DPV-gE protein. The result showed that the fusion pET32a/DPV-gE protein was highly expressed after induction at 30°C with 0.2 mM IPTG for 4.5 h in Rosseta.
We choosed the affinity purification using the immobilized metal affinity chromatography (IMAC) on nickel-nitrilotriacetic acid (Ni2+-NTA) affinity resin. The 6×His-Tag is very useful as a fusion partner for protein purification. 6×His-Tag fusion proteins can be affinity purified under denaturing conditions, which is particularly convenient for proteins expressed as inclusion bodies . After elution with the equilibration buffer containing imidazole, a clear band corresponding to a molecular mass of about 74 kDa was seen on the SDS-PAGE gel following Coomassie blue staining. And Western blotting analysis showed that the fusion pET32a/DPV-gE protein was recognized by the rabbit anti-DPV IgG, it indicated that the protein had good immunogenicity, and the fusion pET32a/DPV-gE protein was used as antigen to produce the rabbit polyclonal antiserum specific for gE. And the fusion pET32a/DPV-gE protein was recognized with the pET32a/DPV-gE antiserum by Western blotting, these results indicated that the recombinant protein gE induced an immunological response and the pET32a/DPV-gE antiserum had a high level of specificity. In addition, the antiserum was examined to react specifically with apparent 54 kDa protein in DPV-infected cells in Western blotting experiments. These results indicated that the antiserum had a high level of reactivity and specificity, and the antiserum was used for further experiments to study the intracellular localization of the DPV gE.
The intracellular localization of DPV gE was examined by indirect immunofluorescence assay and confocal microscopy on DPV-infected DEFs. The data indicated that the protein was detected in the cytoplasm at 5.5 hours post-infection. During the IFA process, the permeabilization time, and the dilution concentration of the primary antibody were two significant factors, the permeabilization time influenced the pET32a/DPV-gE antiserum to penetrate into the cell sufficiently, and the dilution concentration of the primary antibody effected the dense of the gE-specific fluorescence. So we obtained the optimized conditions was with 0.2% (v/v) TrionX-100 in PBS for an additional 15 min at room temperature, and the primary antibody was diluted 1:150 to incubate with the cells at 4°C overnight.
DPV belonged to the Alphaherpesvirinae subfamily of herpesviruses, and possesed a lipidic envelope in which different glycoproteins of viral origin are embedded [28, 29]. About the pathways of Alphaherpesviruses during their intracellular maturation, some reports supported that the nucleocapsids got transient envelops from the inner lamella of nuclear membrane, which would fuse with the membrane of the endoplasmic reticulum. The naked nucleocapsids were released into the cytosol, and they became enveloped during budding into cytosolic membraneous compartments, most probably trans-Golgi network [30, 31]. Some studies had reported that the gE glycoprotein had also been detected in the cytoplasm of the HSV-1-infected cells, VZV-infected cells, and PRV-infected cells. In this report, the result revealed that the DPV gE was targeted to the cytoplasm of DPV-infected cells, similar to the gE homologous protein of HSV-1, VZV-1, and PRV [32–34], and suggested that DPV gE protein might serve similar functions with the gE homologous protein. And some reports had illustrated the role of Tyrosine-containing sorting motifs in regulating the intracellular traffic of membrane proteins [33, 35]. The Tyrosine-containing sorting motifs usually consist of a tetrapeptide bearing the sequence YXXØ (Y is tyrosine, X is any amino acid, and Ø represents any hydrophobic residue) [36, 37]. The DPV gE protein contained YGSY and YNSL in the cytoplasmic domain , we inferred that 2 motifs could mediate the intracellular traffic of DPV gE protein. The research will provide useful clues for further understanding the localization properties of the alphaherpesvirus gE homologs.
Currently, there is little information on the transcription and translation of DPV gE. We studied the transcription of the DPV gE gene using RT-PCR and real-time quantitative PCR. DPV gE earliest transcripts were detected at 5 h post-infection by RT-PCR, and markedly increased at 36 h post-infection. The analysis of real-time quantitative PCR showed that DPV gE earliest transcripts can be detected at 4 h post-infection, and the average relative content of DPV gE transcripts at 36 h post-infection was approximately 40,342 times that of the transcript at 4 h post-infection. It indicated that real-time quantitative PCR was more sensitive than the conventional RT-PCR. We studied the dynamic proliferation of the gE protein expression in DPV-infected DEFs using Western blotting and indirect immunofluorescence assay. The DPV gE protein was first observed at 8 h post-infection, with maximal amounts at 36 h post-infection, and then declining gradually. However, the indirect immunofluorescence assay was highly sensitive. The gE protein specific fluorescence was observed firstly in the cytoplasm region at 5.5 h post infection and increased gradually. These results demonstrated that the accumulation of the gE protein occurred at the late stage of infection. Kocan R M  reported that DPV had a latent period of 6 hours and a maximum virus titer reached at 36 hours in DPV-infected cells at a multiplicity of 2 PFU/cell. However, the number of DPV-infected effected the latent period in virus replication. In this report, the cells were infected with DPV at a multiplicity of 5 PFU/cell, it inferred that the latent period of DPV would be less than 6 h, and the result showed that the gE was detected at 4 h post-infection by real-time quantitative RT-PCR, Guo  had reported that real-time PCR assay for the detection of DPV could detected the 1.0 × 101 copy, so it indicated that gE begun to transcribe at 4 h post infection and would take part in assembling with the envelope to form mature DPV virions.
In conclusion, the DPV gE gene has been successfully expressed in a prokaryotic expression system, and we present the basic characteristics of DPV gE product. The immunofluorescence studies showed that gE mainly localized in the cytoplasm, and DPV gE might share similar functions with its HSV-1, VZV-1, and PRV homolog gE. The real time PCR, RT-PCR, and Western blotting analysis indicated that the accumulation of DPV gE protein was observed at the late stage of infection. These results were especially helpful for the functional analysis of the DPV gE protein.
Materials and methods
DPV CHv strains and the rabbit anti-DPV were provided by Key Laboratory of Animal Disease and Human Health of Sichuan Province. The expression vector pET32a(+) and the host strain Escherichia coli BL21(DE3), BL21(pLysS) and Rosseta were purchased from Novagen. Primers were synthesized at TaKaRa (Dalian, China). Restriction enzymes, EcoRI and XhoI, pMD18-T vector, the Total RNA Isolation System and RNase-free DNase I were purchased from TaKaRa Biotechnology Co. Ltd. The Gel extraction kit purification, and the real-time PCR Master Mix SYBR Green I were purchased from Tiangen Biotechnology Co. Ltd. Horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG, the fluorescein isothiocyanate-conjugated secondary antibody (goat anti-rabbit) and DAB (3'3'-Diaminobenzidine tetrahydrochloride peroxidase) were from Beijing Zhongshan Co. Ltd.
Duck embryo fibroblasts (DEF) were cultured in MEM medium (Gibco-BRL) supplemented with 10% fetal bovine serum (FBS) (Gibco-BRL) at 37°C. For virus infection, MEM medium supplemented with 2-3% FBS was used .
Primer Design and PCR Amplification of the gE Gene
The coding regions of gE gene was amplified by PCR using the primers. The forward primer (P1) is 5'-CGGAATTCATGATGGTTACTTTTATATCTACAG-3', containing a EcoRI site, protective base (underlined) and the first 25nt of the gE ORF, and the reverse primer (P2) 5'-CCGCTCGAGTCAGATGCGGAAACTAGA-3', with a XhoI site, protective base (underlined) and the last 18nt of the gE.
The PCR reagent was composed of 2.5 μl of 10 × reaction buffer, 2.0 μ1 dNTPs (2.5 mM for each of the four dNTPs), 1.0 μl of each primer (20 pM each), 2.0 μl DNA template, 2.0 μl MgCl2, 0.25 μl Taq DNA polymerase (5U/μl), Sterile water was added into the mixture to 25 μl. Reactions were performed at 95°C for 5 min, followed by 30 cycles of 94°C for 45 s, 58°C for 45 s and 72°C for 1.5 min, followed by 72°C for 10 min. The amplified product was verified by 1% agarose gel electrophoresis and analyzed using gel imaging system (Bio-Rad, USA).
Cloning of the gE Gene and Construction of recombinant expression vector
The PCR amplified product of the gE gene was purified by the Gel Extraction kit according to the manufacturer's instructions. The purified product was ligated into pMD18-T vector which was an AT cloning vector at 16°C overnight using T4 DNA ligase. Competent E. coli DH5αcells were transformed with the ligation mixture by the heat shock method. The cells were cultured at 37°C on Luria-Bertani broth plates containing 100 mg/ml ampicillin for 16 h. Then the recombinant plasmid was confirmed by restriction enzyme digestion (EcoRI and XhoI). The correct recombinant plasmid was sent to Dalian TAKARA Biotechnology Co. (China) for sequencing.
The correct recombinant vector was named as pMD18/DPV-gE. Subsequently, the constructed pMD18/DPV-gE was cut with EcoRI and XhoI, and the insert was subcloned into the pET32a(+) expression vector  precut with the same enzymes. Competent E. coli DH5αcells were transformed with the ligation product. Cells were cultured overnight at 37°C on Luria-Bertani broth plates containing 100 mg/ml ampicillin. The subclones were verified by restriction analysis (EcoRI and XhoI). Escherichia coli BL21(pLysS), BL21(DE3) and Rosseta cells were individually transformed with the positive recombinant plasmid and used for protein expression.
Expression and Purification of the recombinant protein
Expression of this fusion protein was regulated by an IPTG-inducible lac operator sequence and a phage T7 promoter. To obtain as much fusion protein as possible, we transformed the recombinant expression into E.coli BL21(DE3), BL21(pLysS) and Rosseta host cells, and optimized the condition for induction. Once an optical density at 600 nm (OD 600nm) of the cultures reached about 0.5, the bacterial culture was induced with different concentrations of IPTG (0.1-1.0 mM) or allowed to grow for 2-6 h at 25, 30, 37°C. The cells were harvested by centrifugation at 10,000 rpm/min for 5 min, and the cell lysate was lysed in SDS sample buffer (0.5 M Tris-HCl, pH 6.8, 50% glycerol, 10% SDS, and 0.05% bromophenol blue, with 100 mM DTT). The pellet was heated at 95°C for 10 min, and analyzed by SDS-PAGE using 12% polyacrylamide gel. The uninduced control culture and the vector control culture were analyzed in parallel.
Recombinant pET32a/DPV-gE protein was purified under denaturing condition using the immobilized metal affinity chromatography (IMAC) on nickel-nitrilotriacetic acid (Ni2+-NTA) affinity resin (Bio-Rad). The induced cells were centrifuged at 10,000 rpm/min for 10 min, and lysed in 20 ml 20 mM Tris-HCl pH 8.0 containing 1.0 mg/ml lysozyme at -20°C overnight. The cell lysate was clarified by centrifugation at 10,000 rpm/min for 20 min at 4°C and the supernatant was discarded, after it was disrupted by an ultrasonic cell disrupter with pulses of 200 W for 30 s intermittence 10 times. The pellet of the inclusion bodies was resuspended in 20 ml cold washing buffer (20 mM Tris-HCl, 2% Triton X-100 (v/v), pH 8.0) under constant stirring for 10 min, then followed by centrifugation at 10,000 rpm/min for 10 min at 4°C, and the above steps were repeated once. Finally, the pellet was solubilized in denaturing buffer (8 M urea, 100 m M NaH2PO4, 10 mM Tris-HCl, pH 8.0). Denatured soluble protein was loaded on the column, and the 6×His-Tag recombinant protein was eluted from the column by 100 ml linear gradient equilibration buffer containing 20-250 mM imidazole, with protein purification system (Bio-Rad, USA). Bound protein fractions were pooled, dialyzed, and concentrated, and the expression yield was analyzed by Bradford assay .
Western Blot Analysis
The pET32a/DPV-gE protein separated on 12% SDS-PAGE gel was transferred to the polyvinylidene difluoride (PVDF) membrane. The membrane was incubated with blocking buffer containing 3% bovine serum albumin (BSA) in TBS (50 mM Tris-HCl, 150 mM NaCl, pH 7.5) for 1 h at 37°C. Subsequently, the membrane was incubated with the serum of the rabbit anti-DPV (diluted 1:200) for 1 h at 4°C overnight, and washed 3 times for 5 min each with TBS containing 0.05% Tween-20 (TBST), and incubated for 2 h with HRP-conjugated goat anti-rabbit IgG (diluted 1:10000). The membrane was again washed with TBST, and developed with substrate solution (DAB 3'3'-Diaminobenzidine tetrahydrochloride peroxidase) for 3 min at 37°C. Finally, the reaction was stopped by the addition of distilled water to strips.
Generation of polyclonal antisera in the rabbits
The purified denatured protein was done by gradient dialysis in 0.85% NaCl solution containing 6, 5, 4, 3, 2 M urea, and changed 3 times over 1 day at 4°C in each solution. Also, aggregation was removed by centrifugation and the supernatant was collected as soluble refolded protein. For the preparation of polyclonal antibodies, the rabbits were immunized intradermally with purified recombinant protein (0.75 mg per rabbit with the addition of Freud's complete adjuvant), after a week, the rabbits were immunized intradermally with purified recombinant protein (1.00 mg per rabbit with the addition of Freud's incomplete adjuvant), the rabbits were immunized subcutaneously with purified recombinant protein (1.00 mg per rabbit with the addition of Freud's incomplete adjuvant) 7 days after the second injection, after 7 days, the rabbits were injected by the vein of the edge of the ears with 0.5 mg per rabbit. Sera were collected 17 days after fourth injections, and stored at -80°C until further use. Control pre-immune serum was obtained before the first injection. The purified pET32a/DPV-gE antiserum was obtained by purification using ammonium sulfate precipitation and High-Q anion-exchange chromatography . Western blottiong analysis was conducted to examine the reactivity and specificity of the pET32a/DPV-gE antiserum.
The expression of gE protein in DPV-infected cells
DEFs were either mock-infected or infected with DPV at a multiplicity of 5 PFU per cell, and harvested at 6, 8, 12, 24, 36, 48 and 60 h post-infection. Cells were lysed in SDS sample buffer, the pellet was heated at 95°Cfor 10 min and size-separated by electrophoresis on 12% SDS-containing polyacrylamide gels followed by transfer of protein onto PVDF membrane. After transferring, the membrane was incubated at 37°C for 60 min with blocking buffer (3% bovine serum albumin in PBST) at 37°C, and subsequently incubated with the purified pET32a/DPV-gE antiserum (diluted 1:150) for 1 h at 37°C. The membrane was washed three times with PBST (PBS plus 0.1% Tween-20), 10 min each and then incubated with horseradish peroxidase-link sheep anti-rabbit IgG (1:10000) for 1 h at 37°C. Following three 10 min washes with PBST, DAB (3'3'-Diaminobenzidine tetrahydrochloride peroxidase) substrate was used as a substrate to visualize the reaction result according to manufacturer's instructions (Beijing Zhong Shan Co. Ltd., China).
Intracellular localization of the gE protein in DPV-infected cells
To characterize the intracellular localization of gE protein, immunofluorescent microscopy analysis was employed with the anti-pET32a/DPV-gE polyclonal antibody as described previously . DEFs grown on glass coverslips were infected with DPV at a multiplicity of 5 PFU/cell. At different times (5.5, 9, 36, 48, and 60 h) post-infection, the cells were collected, and the mock-infected cells were collected. After washing (PBS), the coverslips were fixed immediately for 4% paraformaldehyde for 3 h at 4°C. After permeabilization (PBS, 0.1% triton X-100 for 15 min) and blocking (3% bovine serum albumin in PBS-T for at 4°C overnight), the coverslips were incubated with the pET32a/DPV-gE antiserum for 2 h at 37°C. Following incubation with the primary antibody, the coverslips were washed 3 times in PBS containing 0.2% Tween-20 and stained with fluorescein isothiocyanate-conjugated secondary antibody (goat anti-rabbit, Beijing Zhongshan Co. Ltd) for 30 min. The coverslips were again washed 3 times and stained with 4'6'-diamidino-2-phenylindole (DAPI) for 10 min. To obtain the optimized conditions, the fixed temperature (4°C, 37°C) and time (30 min, 1 h, 4 h and overnight), permeabilization time (5 min, 15 min, 30 min), the blocking buffer (3% bovine serum albumin, 5% bovine serum albumin), the dilution concentration of the primary antibody (1:50, 1:100, 1:150) and incubation time (37°C 30 min, 60 min, 90 min and 4°C overnight) were performed. Finally, the coverslips were mounted onto glass slides with a drop of mounting medium (PBS containing 90% glycerol), and analyzed with Confocal laser scanning microscopy (CLSM, Nikon, Japan).
RNA expression of DPV gE in DPV-infected cells
DEFs were infected with DPV at a multiplicity of 5 PFU per cell. To examine the gE transcription in infected cells in vitro, the total RNA was isolated from mock-infected or DPV-infected cells at different times (4, 5, 6, 8, 12, 16, 24, 36, 48 and 60 h post-infection) by using the Total RNA Isolation System (Takara), and detected by 1.0% agarose gel electrophoresis. The cell volume equivalent amount of total RNA (15 μl) was digested by the RNase-free DNase I (Takara) to eliminate contamination of chromosomal DNA. The concentration of RNA was determined by measuring A260, and the purity was checked by the A260/A280 ratio (greater than 1.8), 100 ng RNA was used as template for RT-PCR. According to the manufacturer's instructions (TaKaRa), the RT reaction was performed in a 10 μl reaction volume.
Based on the nucleotide sequence of the DPV gE gene, the forward primer is 5'-AAAATAACATCGTGGGC-3', and the reverse primer is 5'-TTCGGTAGACTTTAG CATC-3'. Using duck β-actin as the reference gene, the forward primer is 5'-CCGGGCATCGCTGACA-3', and the reverse primer is 5'-GGATTCATCATACTC CTGCTTGCT-3'. RT-PCR was performed in a volume of 25 μl containing 1.0 μl of the forward primer (10 pmol/L), 1.0 of the reverse primer (10 pmol/L), 1.0 μl cDNA template, 12.5 μl PCR Master Mix, and 9.5 μl water. β-actin mRNA expression was determined using the same amount of cDNA as an RNA-competence control. Real time PCR was performed in a volume of 25 μl containing 1.0 μl of the forward primer (10 pmol/L), 1.0 of the reverse primer (10 pmol/L), 1.0 μl cDNA template, 12.5 μl real-time PCR Master Mix SYBR Green I, and 9.5 μl water (all reagents were purchased from TaKaRa). All reactions were performed in triplicate and in at least two independent reactions, and the average relative content of DPV gE gene transcripts was calculated using the 2-ΔΔC t method .
The research were supported by the Changjiang Scholars and Innovative Research Team in University (PCSIRT0848), the earmarked fund for Modern Agro-industry Technology Research System (nycytx-45-12), the Cultivation Fund of the Key Scientific and Technical Innovation Project, Ministry of Education of China (706050), and the Cultivation Fund of the Key Scientific and Technical Innovation Project, department of Education of Sichuan Province (07ZZ028).
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