Wen-Bao Qi

South China Agricultural University, Shengcheng, Guangdong, China

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Publications (14)28.07 Total impact

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    ABSTRACT: Complete genome characterization of porcine circovirus type 2 (PCV2) for bovid origins was still unclear in China. Therefore, in this study, PCV2 full-length genome of buffalo-origin was amplified and analyzed using PCR, DNAStar and MEGA 5.1. Genome size of three distinct PCV2 strains (buffalo1, buffalo2 and buffalo3) was 1767 bp (48.56% G + C), 1767 bp (48.67% G + C) and 1768 bp (48.08% G + C), respectively. At the nucleotide level, their identity varied from 95% to 96% for complete genome, from 97% to 97.8% for ORF1, and from 90.6% to 94.4% for ORF2. At the amino acid level, their identity varied from 98.7% to 99% for ORF1, and from 88% to 94.9% for ORF2. Online Blast analysis showed that buffalo1, buffalo2 and buffalo3 had highest nucleotide identity (varied from 99.77% to 99.83%) with porcine-origin PCV2 strains. Moreover, in the phylogenetic tree, they were divided into three different clusters and belonged to the worldwide accepted genotypes of PCV2b, PCV2c and PCV2a, respectively. To summarize, this study first recorded complete genome information of PCV2 for non-porcine origins in China.
    Full-text · Article · Oct 2014 · Infection Genetics and Evolution
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    ABSTRACT: MicroRNAs (miRNAs) are a class of endogenous non-coding small RNAs of 18-22-nucleotides in length that regulate gene expression at the post-transcriptional level. The objective of this study was to examine the differences in the miRNA expression profiles of the lungs and trachea of beagle dogs infected with canine influenza virus (CIV). Total RNA was isolated from lung and trachea tissues of beagle dogs infected and non-infected with H3N2 CIV at 4 dpi. A total of 41,512,315 and 39,107,475 reads were obtained from the lung and trachea, respectively. Out of a total 288 dog miRNAs available in miRBase, 227 and 236 miRNAs were detected in the infected (Fg) and the non-infected lungs (Fc), respectively, whereas 242 miRNAs were detected in both the infected (Qg) and the non-infected trachea (Qc). From these, 34 and 45 miRNAs were differentially expressed in the lungs and trachea between the infected and non-infected dogs, respectively. More miRNAs were highly expressed in the non-infected tissues than in the infected tissues. miR-143 was the most abundantly expressed miRNA in the four samples, followed by let-7. In total, 252, 234, 196 and 235 novel miRNAs were identified in the Fc, Fg, Qc, and Qg groups, respectively. To our knowledge, this is the first study examining the miRNA gene expression in CIV infected dogs using the Solexa sequencing approach. We have revealed the existence of a large number miRNAs that are affected by CIV infection as well as identified some potentially new miRNAs. These findings will help us better understand the host-CIV interaction and its relationship to pathogenesis, as well as contribute to the prevention and control of CIV.
    No preview · Article · Dec 2013 · Infection, genetics and evolution: journal of molecular epidemiology and evolutionary genetics in infectious diseases
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    ABSTRACT: Influenza A viruses occasionally cause large epidemics and kill thousands every year. While little is known about the mechanism of cell fusion in diseases, especially influenza virus infected and protection from Amaryllidaceae Alkaloids. The two compounds lyconne (AA1) and haemanthamme (AA3) were obtained from bulbs ofL. radiate, exhibited anti-influenza activity after influenza virus entry cells. The two compounds were investigated for in vitro displaying different levels of resistance to pro-apoptotic stimuli. Seven influenza viruses were used, A/CK/GD/178/04 (H 5N, 178), A/DK/GD/212/04 (H 5N l5 212), A/swine/GD/166/06 (H 3N 2,166), A/CK/HN/170/03 (H 1N 1, 170), A/Puerto Rico/8/34 (H 1N 1, PR8), A/Ck/GD/400/07 (H 9N 2, 400), A/Ck/GD/228/04 (H 9N2, 228), the two compounds exhibited potency in the single-digit micromolar range. The studies also showed that AA1 and A A3 exerted their in vitro anti-influenza activity through cytostatic rather than cytotoxic effects. Many viruses interact with the host cells to change their own growth which they favor the speed. The cells infected with virus, growth of MDCK cells was slowed down by arresting cell cycle at Gl/S phase. With the compound treated, the growth cycle was decreased in S phase. With H 5N 1, influenza virus treated, the cytoskeleton of cells was changed while with the compound treated the protection of cytoskeleton was obviously protected. The data showed differences between drug treated cells and virus infected cells, provided a basis to further explore cell fusion and anti-influenza mechanism of the two compounds.
    No preview · Article · Dec 2012 · Journal of Animal and Veterinary Advances
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    ABSTRACT: Pigs serve as major reservoirs of HINl and H3N2 influenza viruses which are endemic in pig populations world-wide and are responsible for one of the most prevalent respiratory diseases in pigs. Furthermore, swine H9N2 influenza viruses might be a potential threat to human health and continuing to carry out swine influenza virus surveillance in China is of great significance. From March 2010-2011, researchers carried out serological surveillance of swine influenza in seven cities located Guangdong province in South China. The serological results indicated that antibodies to HINl swine influenza virus in the swine population were high with a 34.6% (226/653) positive rate whereas antibodies to H3N2 swine influenza virus were low with a 16.4% (107/653) positive rate. Autibodies to H9N2 swine influenza virus were very low with a 1.4% (9/653) positive rate. HINI influenza viruses were more dominant in the pig population than H3N2 influenza viruses in South China. H9N2 influenza virus in the pigs only send out the phenomenon in South China. According to reports in the virology and molecular epidemiological studies, the South China coastal areas of the global influenza research in key areas is the region of finding new influenza subtypes in the world and influenza outbreak Therefore, the presence of H9N2, HI NI and H3N2 subtypes in pigs of Chnia and the potential public health significance have become the focus of attention of the global influenza research. After the outbreak of the flu pandemic in 2009, researchers had done a serological smvey of large-scale farms in seven cities in Guangdong province. The results showed that swine influenza virus infections are more common in the surveyed farms: all farms were infected by swine influenza virus infection and more than half of the pigs present antibody-positive.
    No preview · Article · Dec 2012 · Journal of Animal and Veterinary Advances
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    ABSTRACT: Please cite this paper as: He et al. (2013) Amaryllidaceae alkaloids inhibit nuclear‐to‐cytoplasmic export of ribonucleoprotein (RNP) complex of highly pathogenic avian influenza virus H5N1. Influenza and Other Respiratory Viruses 7(6), 922–931. Background Few drugs are currently licensed to treat influenza A infection, and new therapies are needed, especially for highly pathogenic strains. Traditional medicinal plants, such as Lycoris radiata, are a potential source of new antiviral agents. Objective To test 15 Amaryllidaceae alkaloids isolated from the bulbs of L. radiata in vitro for antiviral activities against influenza virus type A, A/Chicken/GuangDong/178/2004 (H5N1, 178). Methods Antiviral activities of the compounds were tested in time‐of‐addition assays, hemagglutination inhibition (HI) assays, neuraminidase (NA) activity assays, and viral entry inhibition assays using H5N1‐HIV pseudoviruses. Effects of the compounds on localization and activity of the viral ribonucleoprotein (RNP) were determined by immunofluorescence and an RNP minigenome assay, respectively. Results Among the alkaloids, lycorine (AA1), hippeastrine (AA2), hemanthamine (AA3) and 11‐hydroxy vittatine (AA4) exhibited antiviral activities, with EC90 values of 0·52, 82·07, 4·15, and 13·45 μm, respectively. These compounds did not affect the function of the outer membrane proteins or the viral entry process and viral RNP activity. As AA1 and AA3 exhibited stronger antiviral activities, they were further analyzed. Intracellular nucleoprotein (NP) localization showed that AA1 and AA3 inhibited the RNP complex in the nucleus at an early stage of a single‐round and multi‐round of replication. Conclusion Four Amaryllidaceae alkaloids were first determined that could exert anti‐influenza activities after virus entry into cells. Furthermore, AA1 and AA3 could inhibit nuclear‐to‐cytoplasmic export of the RNP complex of virus replication. Thus, these compounds may be developed further as anti‐influenza drug candidates.
    Full-text · Article · Nov 2012 · Influenza and Other Respiratory Viruses
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    ABSTRACT: Reports of influenza A virus infections in dogs has received considerable attention from veterinarians, virologists, and epidemiologists. Interaction between influenza viral hemagglutinin and cell oligosaccharides containing sialic acid residues results in infection. Sialic acids have an α-2,3-linkage to the penultimate galactose in the avian influenza virus receptor and an α-2,6-linkage in the human receptor. To date, there are no detailed data on the tissue distribution or histological features of either type of sialic acid-linked influenza virus receptors in beagle dogs, which are common laboratory animals and pets. We conducted the current study to visualize the in situ tissue distribution of both sialic acid-linked influenza virus receptors in various organs of beagle dogs using Maackia amurensis lectin II and Sambucus nigra agglutinin. Both α-2,3- and α-2,6-sialic acid-linked receptors were detected in the endothelial cells of the respiratory tract and other organs. Endothelial cells of most gastrointestinal organs were negative for α-2,3-sialic acid-linked receptors in the dogs. Our results suggested that these canine organs may be affected by influenza virus infection. The findings from our study will also help evaluate the occurrence and development of influenza virus infections in dogs.
    No preview · Article · Sep 2012 · Journal of Veterinary Science
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    ABSTRACT: We report here the complete genomic sequence of an avian-like H4N8 swine influenza virus containing an H5N1 avian influenza virus segment from swine in southern China. Phylogenetic analyses of the sequences of all eight viral RNA segments demonstrated that these are wholly avian influenza viruses of the Asia lineage. To our knowledge, this is the first report of interspecies transmission of an avian H4N8 influenza virus to domestic pigs under natural conditions.
    Preview · Article · Sep 2012 · Journal of Virology
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    ABSTRACT: We report here the complete genomic sequence of a novel avian-like H3N2 swine influenza virus containing an H5N1 highly pathogenic avian influenza virus segment that was obtained from swine in southern China. Phylogenetic analysis indicated that this virus might originate from domestic aquatic birds. The sequence information provided herein suggests that continuing study is required to determine if this virus can be established in the swine population and pose potential threats to public health.
    Preview · Article · Sep 2012 · Journal of Virology
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    ABSTRACT: The Na(+)/H(+) exchanger 1 (NHE1) transmembrane protein regulates intracellular pH, cell survival, cell growth, cell differentiation and plays a critical role in the progression of some diseases, including the pathogenesis of J avian leukosis. The chicken is an ideal model to study the function of NHE1 because it has developed highly efficient Na(+)-absorptive mechanisms in its small and large intestines. To date, there has been no detailed expression analysis to determine NHE1 expression in various tissues of the chicken. We determined the mRNA and protein expression levels of avian NHE1 by real-time quantitative PCR and immunohistochemical analysis. NHE1 mRNA was detected in all chicken tissues examined. Protein expression levels varied widely among tissues and did not always correlate with mRNA expression. Determining the mRNA and protein of NHE1 expression patterns in chicken should help to delineate the NHE1 role in different tissues and its contribution to physiological and pathological processes. These data provide the basis for examining the distinct function of chicken NHE1 compared with its mammalian counterpart.
    No preview · Article · Sep 2011 · Biochemical Genetics
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    ABSTRACT: Two swine influenza (SI) H1N1 virus was isolated from a pig during a severe outbreak of respiratory disease in south China. The two H1N1 influenza viruses were classical SI virus. A/swine/Guangdong/L6/09 is classical SI virus of recent years, which is of the main SI virus in China. Howere, A/swine/Guangdong/L3/09 was closet to A/swine/Iowa/1931, which was the first isolated SI virus and had demonstrated significant pathogenicity in animal models. The results of phylogenetic analysis of A/swine/Guangdong/L3/09 showed a close relationship with the 1918 pandemic virus. The results suggested that the previous SI virus appeared again. Whether, it brought a new pandemic to pigs deserves more attention.
    Full-text · Article · Jun 2011 · Indian Journal of Virology
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S5: SDS-PAGE analysis of supernatant or inclusion bodies (four compounds were added to binding buffer). Lane M: Protein Markers; Supernatant (lane 1) or Precipitation (lane 2) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the five compounds: β-mercaptoethanol, urea, Tween 20, glycerol, and SDS; Supernatant (lane 3) or Precipitation (lane 4) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the 5 compounds with the exception of urea; Supernatant (lane 5) or Precipitation (lane 6) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the 5 compounds with the exception of Tween 20; Supernatant (lane 7) or Precipitation (lane 8) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the 5 compounds with the exception of β-mercaptoethanol; Supernatant (lane 9) or Precipitation (lane 10) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the 5 compounds with the exception of glycerol; Supernatant (lane 11) or Precipitation (lane 12) after ultrasonic disruption of the tD5-producing cells that used binding buffer with the 5 compounds with the exception of SDS; Supernatant (lane 13) or Precipitation (lane 14) after ultrasonic disruption of the tD5-producing cells that used binding buffer without the compounds.
    Preview · Dataset · Mar 2011
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S1: SDS-PAGE analysis of the expression of tD4 (a) or tD5 (b) products at different times. Lane M: Protein Markers; lane 1: pET28a non-induced; lane 2: pET28a induced for 4 h (1.0 mmol/L); lane 3: pET-28a-tD4 or pET-28a-tD5 non-induced; lane 4: pET-28a-tD4 or pET-28a-tD5 induced for 1 h (1.0 mmol/L); lane 5: pET-28a-tD4 or pET-28a-tD5 induced for 2 h (1.0 mmol/L); lane 6: pET-28a-tD4 or pET-28a-tD5 induced for 3 h (1.0 mmol/L); lane 7: pET-28a-tD4 or pET-28a-tD5 induced for 4 h (1.0 mmol/L); lane 8: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (1.0 mmol/L); lane 9: pET-28a-tD4 or pET-28a-tD5 induced for 6 h (1.0 mmol/L).
    Preview · Dataset · Mar 2011
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S6: SDS-PAGE analysis of supernatant or inclusion bodies after ultrasonic disruption of the cells from the production of GST recombinant fusion protein. Lane M: Protein Markers; lane 1: Supernatant after ultrasonic disruption of the GST-A-producing cells that used the binding buffer without the compounds; lane 2: Precipitation after ultrasonic disruption of the GST-A-producing cells that used the binding buffer without the compounds; lane 3: Supernatant after ultrasonic disruption of the cells from the production of GST-A using binding buffer with the following compounds: β-mercaptoethanol, urea, Tween 20, glycerol, and SDS; lane 4: Precipitation after ultrasonic disruption of the GST-A-producing cells that used binding buffer with the compounds; lane 5: Supernatant after ultrasonic disruption of the GST-B-producing cells that used the binding buffer without the compounds; lane 6: Precipitation after ultrasonic disruption of the GST-B-producing cells that used the binding buffer without the compounds; lane 7: Supernatant after ultrasonic disruption of the GST-B-producing cells that used the binding buffer with the compounds; lane 8: Precipitation after ultrasonic disruption of the GST-B-producing cells that used the binding buffer with the compounds.
    Preview · Dataset · Mar 2011
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S2: SDS-PAGE analysis of the expression of tD4 (a) or tD5 (b) products with different concentrations of isopropyl beta-D-thiogalactopyranoside (IPTG). Lane M: Protein Markers; lane 1: pET28a non-induced; lane 2: pET28a induced for 5 h (1.0 mmol/L); lane 3: pET-28a-tD4 or pET-28a-tD5 non-induced; lane 4: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (0.2 mmol/L); lane 5: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (0.4 mmol/L); lane 6: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (0.6 mmol/L); lane 7: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (0.8 mmol/L); lane 8: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (1.0 mmol/L); lane 9: pET-28a-tD4 or pET-28a-tD5 induced for 5 h (1.2 mmol/L).
    Preview · Dataset · Mar 2011
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S4: SDS-PAGE analysis of supernatant or inclusion bodies (one compound was added alone to binding buffer). Lane M: Protein Markers; Supernatant (lane 1) or Precipitation (lane 2) after ultrasonic disruption of the tD5-producing cells that used binding buffer without the compounds; Supernatant (lane 3) or Precipitation (lane 4) after ultrasonic disruption of the tD5-producing cells that used binding buffer only with SDS; Supernatant (lane 5) or Precipitation (lane 6) after ultrasonic disruption of the tD5-producing cells that used binding buffer only with glycerol; Supernatant (lane 7) or Precipitation (lane 8) after ultrasonic disruption of the tD5-producing cells that used binding buffer only with β-mercaptoethanol; Supernatant (lane 9) or Precipitation (lane 10) after ultrasonic disruption of the tD5-producing cells that used binding buffer only with Tween 20; Supernatant (lane 11) or Precipitation (lane 12) after ultrasonic disruption of the tD5-producing cells that used binding buffer only with urea; Supernatant (lane 13) or Precipitation (lane 14) after ultrasonic disruption of the tD5-producing cells that used binding buffer containing the five compounds: β-mercaptoethanol, urea, Tween 20, glycerol, and SDS.
    Preview · Dataset · Mar 2011
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    Zong-Xi Cao · Fu-Rong Zhao · Kun Jia · Wei-Wei Sun · Ming-Fei Yan · Si-Hu Guo · Pei-Rong Jiao · Wen-Bao Qi · Gui-Hong Zhang
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    ABSTRACT: Figure S3: SDS-PAGE analysis of samples taken during the purification of tD4 (a) or tD5 (b) protein. Lane M: Protein Markers; lane 1: Supernatant after ultrasonic disruption; lane 2: Precipitation after ultrasonic disruption; lane 3: Collected flow-though during loading of tD4 or tD5 protein; lanes 4-6: Collected flow-though from washing the gravity-flow columns with binding buffer; lanes 7-8: Collected flow-though from washing the gravity-flow columns with elution buffer.
    Preview · Dataset · Mar 2011
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    ABSTRACT: Porcine reproductive and respiratory syndrome virus (PRRSV) has been acknowledged as one of the most important agents affecting swine. The scavenger receptor CD163 is one of the important entry mediators for PRRSV. The tD4 and tD5 CD163 genes were amplified, and the PCR products were cloned into pET-28a(+) (designated pET-28a-tD4 and pET-28a-tD5, respectively). The plasmids pET-28a-tD4 and pET-28a-tD5 were then transformed into the E. coli BL21 (DE3) strain and expressed by adding 1 mmol/L of isopropyl-beta-D-thiogalactopyranoside. The proteins were highly expressed in the supernatant from the tD4- and tD5-producing cells that were incubated with a binding buffer containing the following compounds: β-mercaptoethanol, urea, Tween 20, glycerol, and SDS, while they were rarely expressed in the supernatant from the tD4- and tD5-producing cells that were incubated with binding buffer without the compounds. The tD4 and tD5 proteins were purified, and BALB/c mice were immunized with the purified proteins. Western blotting analysis showed that the tD4 and tD5 proteins were capable of reacting with tD5 antibodies; the titer of both the tD4 and tD5 antiserums was 1:160 against the tD5 protein, as shown by ELISA. These studies provide a new way for the purification of proteins expressed in inclusion bodies and the preparation of the corresponding antibodies.
    Full-text · Article · Mar 2011 · Virology Journal
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    ABSTRACT: Influenza is a pandemic contagious disease and causes human deaths and huge economic destruction of poultry in the world. In order to control and prevent influenza, mainly type A, influenza vaccine for human and poultry were available since the 1940s and 1920s, respectively. In the development of vaccine production, influenza viruses were cultured originally from chicken embryos to anchorage-dependent cell lines, such as MDCK and Vero. The anchorage-independent lines have also been used to produce influenza virus, such as PER.C6 and engineering modified MDCK and Vero. During the process of influenza vaccine production, the common problem faced by all producers is how to improve the titer of influenza virus. This paper focuses on the developments of cell culture for influenza virus vaccine production, limitations of cell culture, and relative strategies for improvement virus yields in cell-culture systems.
    Full-text · Article · Nov 2010 · Applied Microbiology and Biotechnology
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    ABSTRACT: Eight full-length genes of an avian influenza virus Chinese isolate of H9N2 subtype, A/Chicken/Guangdong/HL/2006 (H9N2) (abbreviated as Ck/GD/HL/06), were amplified by RT-PCR, including the 5' and 3' non-coding region. All the genes were cloned and sequenced. The phylogenetic analysis results showed the HA gene of Ck/GD/HL/06 was located in the same phylogenetic clade as Dk/HK/Y280/97 (H9N2), while the Dk/HK/Y280/97-like viruses had been predominately isolated from chickens in mainland China. After the analysis of glycosylation sites and receptor-binding sites in the HA, it was shown that the HA of Ck/GD/HL/06 exhibited the common feature of H9 subtype avian influenza virus isolated from China, but the leucine (Leu) residue at the amino acid position 226 indicated the potential of binding with SA alpha,2-6 receptor. The three internal genes of Ck/GD/HL/06 (PB1, PA and NP) had the highest nucleotide identity with A/Viet Nam/1203/2004 (abbreviated A/VN/1203/04) isolate, which was shown to be transmitted from chickens to human and caused lethal infection in human. No analogous H9N2 strains was reported in previous studies. Based on the high similarity of Ck/GD/HL/06 three genes to A/VN/1203/04, it was suggested that the possibility of generating new highly pathogenic H5N1 AIVs by recombination was worthy of our attention. Further studies should be needed for molecular epidemiologic surveillance of H9N2 AIV in the south China for a long time.
    No preview · Article · May 2010 · Bing du xue bao = Chinese journal of virology / [bian ji, Bing du xue bao bian ji wei yuan hui]
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    ABSTRACT: Japanese encephalitis virus (JEV), a mosquito-borne flavivirus, causes an acute infection of the central nervous system resulting in encephalitis of humans and many kinds of animals. NS5, the largest and most conserved flavivirus protein, is homologous to methyltransferase and RNA-dependent RNA polymerase. RNA interference is an effective anti-viral strategy to inhibit viral replication in vitro. In this study, four short hairpin RNA (shRNA) expression vectors (pS4.1-NS5-201, pS4.1-NS5-455, pS4.1-NS5-699, and pS4.1-NS5-804) targeting the NS5 gene of JEV were employed to target and destroy JEV transcripts. The four shRNAs expression plasmids were individually co-transfected into 293T cells with the plasmid pNS5-EGFP expressing NS5 fused to enhanced green fluorescent protein. The expression level of NS5 was evaluated by fluorescence microscopy, flow cytometry, real time RT-PCR, and Western blot. The four shRNA expression plasmids were also transfected into BHK-21 cells to examine their inhibition of viral replication by indirect immunofluorescence, real time RT-PCR, and Western blot. The results provided strong evidence that shRNAs targeting the NS5 gene could specifically and efficiently inhibit JEV replication. Three out of four plasmids were highly efficient at inhibiting viral replication, including pS4.1-NS5-455, pS4.1-NS5-699, and pS4.1-NS5-804. This was especially true for pS4.1-NS5-699, which reduced the levels of virus RNA and protein the most. Our data suggest that shRNAs could be used as a tool to inhibit JEV replication in vivo.
    No preview · Article · Apr 2008 · Virus Research

Publication Stats

76 Citations
28.07 Total Impact Points

Institutions

  • 2010-2014
    • South China Agricultural University
      • College of Veterinary Medicine
      Shengcheng, Guangdong, China
  • 2012
    • Yunnan Agricultural University
      Panlong, Shaanxi, China
  • 2008
    • Harbin Veterinary Research Institute
      Charbin, Heilongjiang Sheng, China