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h5n2 viruses  (ATCC)


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    Structured Review

    ATCC h5n2 viruses
    Sequence homology of the whole A/Wild duck/South <t> Korea/KNU18-28/2018 </t> <t> (A/H5N2) </t> genome.
    H5n2 Viruses, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 917 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/h5n2+viruses/pmc08619638-123-2-37?v=ATCC
    Average 96 stars, based on 917 article reviews
    h5n2 viruses - by Bioz Stars, 2026-08
    96/100 stars

    Images

    1) Product Images from "Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018"

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    Journal: Viruses

    doi: 10.3390/v13112192

    Sequence homology of the whole A/Wild duck/South  Korea/KNU18-28/2018   (A/H5N2)  genome.
    Figure Legend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-28/2018 (A/H5N2) genome.

    Techniques Used: Sequencing

    Sequence homology of the whole A/Bean Goose/South  Korea/KNU18-86/2018   (A/H5N2)  genome.
    Figure Legend Snippet: Sequence homology of the whole A/Bean Goose/South Korea/KNU18-86/2018 (A/H5N2) genome.

    Techniques Used: Sequencing

    Sequence homology of the whole A/Wild duck/South  Korea/KNU18-93/2018   (A/H5N2)  genome.
    Figure Legend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-93/2018 (A/H5N2) genome.

    Techniques Used: Sequencing

    Putative origins of the genes comprising the KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.
    Figure Legend Snippet: Putative origins of the genes comprising the KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Techniques Used:

    Phylogenetic tree analysis of NS gene segment based on the nucleotide sequences. MEGA-X software using maximum likelihood method with bootstrap replication (1000 bootstraps) was used to generate the phylogenetic tree. Red color: novel H5N2 isolates, blue color: Korean strains, purple color: H5N2 highly pathogenic avian influenza viruses (HPAIVs), and green color: H5N3 strain isolated at the same surveillance time.
    Figure Legend Snippet: Phylogenetic tree analysis of NS gene segment based on the nucleotide sequences. MEGA-X software using maximum likelihood method with bootstrap replication (1000 bootstraps) was used to generate the phylogenetic tree. Red color: novel H5N2 isolates, blue color: Korean strains, purple color: H5N2 highly pathogenic avian influenza viruses (HPAIVs), and green color: H5N3 strain isolated at the same surveillance time.

    Techniques Used: Software, Isolation

    Hypothesis of the ancestor of each gene segment evolution of ( A ) KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and ( B ) KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.
    Figure Legend Snippet: Hypothesis of the ancestor of each gene segment evolution of ( A ) KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and ( B ) KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Techniques Used:

    Comparison between the hemagglutinin (HA) receptor-binding sites and neuraminidase (NA) of the three novel avian influenza  H5N2 viruses  and those of low pathogenic and highly pathogenic H5 viruses.
    Figure Legend Snippet: Comparison between the hemagglutinin (HA) receptor-binding sites and neuraminidase (NA) of the three novel avian influenza H5N2 viruses and those of low pathogenic and highly pathogenic H5 viruses.

    Techniques Used: Comparison

    Amino acid mutation analysis of eight gene segments responsible for enhancing polymerase activity, viral transmissibility, and virulence of the three novel  H5N2 viruses.
    Figure Legend Snippet: Amino acid mutation analysis of eight gene segments responsible for enhancing polymerase activity, viral transmissibility, and virulence of the three novel H5N2 viruses.

    Techniques Used: Mutagenesis, Activity Assay, Mouse Assay, Virus

    Growth kinetics replication of three novel H5N2 isolates in MDCK cells. Five kinds of viruses were infected with 0.01 multiplicity of infection (MOI) into MDCK monolayers. The virus supernatants were collected at different time points each 12 h until 71 h post-infection (hpi). The viral replication titers were then determined by the TCID 50 assay combined ELISA for detecting the nucleoprotein (NP) viral antigen. *, p < 0.05; **, p < 0.01; and ***, p < 0.001 showing comparison with H5N3 control.
    Figure Legend Snippet: Growth kinetics replication of three novel H5N2 isolates in MDCK cells. Five kinds of viruses were infected with 0.01 multiplicity of infection (MOI) into MDCK monolayers. The virus supernatants were collected at different time points each 12 h until 71 h post-infection (hpi). The viral replication titers were then determined by the TCID 50 assay combined ELISA for detecting the nucleoprotein (NP) viral antigen. *, p < 0.05; **, p < 0.01; and ***, p < 0.001 showing comparison with H5N3 control.

    Techniques Used: Infection, Virus, Enzyme-linked Immunosorbent Assay, Comparison, Control

    In vivo pathogenicity of three novel H5N2 isolates in mouse model. The BALB/c mice were intranasally challenged with three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) at titer 10 5 EID 50 /mouse. H1N1 and H5N3 virus strains were used as controls. Mouse bodyweight change ( A ) and survival rate ( B ) were observed for 14 days post-infection (dpi). Bodyweight is presented as a % change from those of the same mice at day 0 ( n = 5). ( C ) The viral titer mean values in the mouse lung ( n = 3) were determined at 3, 6, and 14 dpi. ( D ) Mean lung weight of normal mice and infected mice at 6 dpi ( n = 3) was observed before examining the histology of lung inflammation by hematoxylin and eosin (H&E) staining. **, p < 0.01; ***, p < 0.001.
    Figure Legend Snippet: In vivo pathogenicity of three novel H5N2 isolates in mouse model. The BALB/c mice were intranasally challenged with three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) at titer 10 5 EID 50 /mouse. H1N1 and H5N3 virus strains were used as controls. Mouse bodyweight change ( A ) and survival rate ( B ) were observed for 14 days post-infection (dpi). Bodyweight is presented as a % change from those of the same mice at day 0 ( n = 5). ( C ) The viral titer mean values in the mouse lung ( n = 3) were determined at 3, 6, and 14 dpi. ( D ) Mean lung weight of normal mice and infected mice at 6 dpi ( n = 3) was observed before examining the histology of lung inflammation by hematoxylin and eosin (H&E) staining. **, p < 0.01; ***, p < 0.001.

    Techniques Used: In Vivo, Virus, Infection, Staining

    Histology of lung inflammation examined by hematoxylin and eosin (H&E) staining. BALB/c mice were intranasally challenged with 10 5 EID 50 /mouse ( n = 3) of three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) and two control virus strains (H1N1 and H5N3). The infected mouse lungs were collected for H&E staining at 6 dpi (scale bar, 100 µm; original magnification, 40×).
    Figure Legend Snippet: Histology of lung inflammation examined by hematoxylin and eosin (H&E) staining. BALB/c mice were intranasally challenged with 10 5 EID 50 /mouse ( n = 3) of three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) and two control virus strains (H1N1 and H5N3). The infected mouse lungs were collected for H&E staining at 6 dpi (scale bar, 100 µm; original magnification, 40×).

    Techniques Used: Staining, Control, Virus, Infection



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    Image Search Results


    Sequence homology of the whole A/Wild duck/South  Korea/KNU18-28/2018   (A/H5N2)  genome.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-28/2018 (A/H5N2) genome.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Sequencing

    Sequence homology of the whole A/Bean Goose/South  Korea/KNU18-86/2018   (A/H5N2)  genome.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Sequence homology of the whole A/Bean Goose/South Korea/KNU18-86/2018 (A/H5N2) genome.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Sequencing

    Sequence homology of the whole A/Wild duck/South  Korea/KNU18-93/2018   (A/H5N2)  genome.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-93/2018 (A/H5N2) genome.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Sequencing

    Putative origins of the genes comprising the KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Putative origins of the genes comprising the KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques:

    Phylogenetic tree analysis of NS gene segment based on the nucleotide sequences. MEGA-X software using maximum likelihood method with bootstrap replication (1000 bootstraps) was used to generate the phylogenetic tree. Red color: novel H5N2 isolates, blue color: Korean strains, purple color: H5N2 highly pathogenic avian influenza viruses (HPAIVs), and green color: H5N3 strain isolated at the same surveillance time.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Phylogenetic tree analysis of NS gene segment based on the nucleotide sequences. MEGA-X software using maximum likelihood method with bootstrap replication (1000 bootstraps) was used to generate the phylogenetic tree. Red color: novel H5N2 isolates, blue color: Korean strains, purple color: H5N2 highly pathogenic avian influenza viruses (HPAIVs), and green color: H5N3 strain isolated at the same surveillance time.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Software, Isolation

    Hypothesis of the ancestor of each gene segment evolution of ( A ) KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and ( B ) KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Hypothesis of the ancestor of each gene segment evolution of ( A ) KNU18-28 (A/Wild duck/South Korea/KNU18-28/2018 (H5N2)), KNU18-86 (A/Bean Goose/South Korea/KNU18-86/2018 (H5N2)), and ( B ) KNU18-93 (A/Wild duck/South Korea/KNU18-93/2018 (H5N2)) strains.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques:

    Comparison between the hemagglutinin (HA) receptor-binding sites and neuraminidase (NA) of the three novel avian influenza  H5N2 viruses  and those of low pathogenic and highly pathogenic H5 viruses.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Comparison between the hemagglutinin (HA) receptor-binding sites and neuraminidase (NA) of the three novel avian influenza H5N2 viruses and those of low pathogenic and highly pathogenic H5 viruses.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Comparison

    Amino acid mutation analysis of eight gene segments responsible for enhancing polymerase activity, viral transmissibility, and virulence of the three novel  H5N2 viruses.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Amino acid mutation analysis of eight gene segments responsible for enhancing polymerase activity, viral transmissibility, and virulence of the three novel H5N2 viruses.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Mutagenesis, Activity Assay, Mouse Assay, Virus

    Growth kinetics replication of three novel H5N2 isolates in MDCK cells. Five kinds of viruses were infected with 0.01 multiplicity of infection (MOI) into MDCK monolayers. The virus supernatants were collected at different time points each 12 h until 71 h post-infection (hpi). The viral replication titers were then determined by the TCID 50 assay combined ELISA for detecting the nucleoprotein (NP) viral antigen. *, p < 0.05; **, p < 0.01; and ***, p < 0.001 showing comparison with H5N3 control.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Growth kinetics replication of three novel H5N2 isolates in MDCK cells. Five kinds of viruses were infected with 0.01 multiplicity of infection (MOI) into MDCK monolayers. The virus supernatants were collected at different time points each 12 h until 71 h post-infection (hpi). The viral replication titers were then determined by the TCID 50 assay combined ELISA for detecting the nucleoprotein (NP) viral antigen. *, p < 0.05; **, p < 0.01; and ***, p < 0.001 showing comparison with H5N3 control.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Infection, Virus, Enzyme-linked Immunosorbent Assay, Comparison, Control

    In vivo pathogenicity of three novel H5N2 isolates in mouse model. The BALB/c mice were intranasally challenged with three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) at titer 10 5 EID 50 /mouse. H1N1 and H5N3 virus strains were used as controls. Mouse bodyweight change ( A ) and survival rate ( B ) were observed for 14 days post-infection (dpi). Bodyweight is presented as a % change from those of the same mice at day 0 ( n = 5). ( C ) The viral titer mean values in the mouse lung ( n = 3) were determined at 3, 6, and 14 dpi. ( D ) Mean lung weight of normal mice and infected mice at 6 dpi ( n = 3) was observed before examining the histology of lung inflammation by hematoxylin and eosin (H&E) staining. **, p < 0.01; ***, p < 0.001.

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: In vivo pathogenicity of three novel H5N2 isolates in mouse model. The BALB/c mice were intranasally challenged with three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) at titer 10 5 EID 50 /mouse. H1N1 and H5N3 virus strains were used as controls. Mouse bodyweight change ( A ) and survival rate ( B ) were observed for 14 days post-infection (dpi). Bodyweight is presented as a % change from those of the same mice at day 0 ( n = 5). ( C ) The viral titer mean values in the mouse lung ( n = 3) were determined at 3, 6, and 14 dpi. ( D ) Mean lung weight of normal mice and infected mice at 6 dpi ( n = 3) was observed before examining the histology of lung inflammation by hematoxylin and eosin (H&E) staining. **, p < 0.01; ***, p < 0.001.

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: In Vivo, Virus, Infection, Staining

    Histology of lung inflammation examined by hematoxylin and eosin (H&E) staining. BALB/c mice were intranasally challenged with 10 5 EID 50 /mouse ( n = 3) of three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) and two control virus strains (H1N1 and H5N3). The infected mouse lungs were collected for H&E staining at 6 dpi (scale bar, 100 µm; original magnification, 40×).

    Journal: Viruses

    Article Title: Genetic Characterization and Pathogenesis of Three Novel Reassortant H5N2 Viruses in South Korea, 2018

    doi: 10.3390/v13112192

    Figure Lengend Snippet: Histology of lung inflammation examined by hematoxylin and eosin (H&E) staining. BALB/c mice were intranasally challenged with 10 5 EID 50 /mouse ( n = 3) of three novel H5N2 isolates (KNU18-28, KNU18-86, and KNU18-93) and two control virus strains (H1N1 and H5N3). The infected mouse lungs were collected for H&E staining at 6 dpi (scale bar, 100 µm; original magnification, 40×).

    Article Snippet: Three isolated H5N2 viruses (A/Wild duck/South Korea/KNU18-28/2018, A/Bean Goose/South Korea/KNU18-86/2018, and A/Wild duck/South Korea/KNU18-93/2018) together with two reference strains (human-origin H1N1 (A/California/04/2009) and H5N3 (A/spot-billed duck/Korea/KNU SYG06/2006)) were infected into the Madin–Darby canine kidney (MDCK) cell line (American Type Culture Collection) to examine the viral replication capacity in mammalian cells.

    Techniques: Staining, Control, Virus, Infection

    The profile of generated  H5N2  reassortant viruses.

    Journal: Viruses

    Article Title: Development of American-Lineage Influenza H5N2 Reassortant Vaccine Viruses for Pandemic Preparedness

    doi: 10.3390/v11060543

    Figure Lengend Snippet: The profile of generated H5N2 reassortant viruses.

    Article Snippet: Eight plasmids which contained NA and modified HA genes from an H5N2 virus and six internal genes from the Vero-15 virus were transfected into Vero cells to generate H5N2 vaccine viruses by electroporation (Bio-RAD Gene Pulser Xcell system, Hercules, CA, USA).

    Techniques: Generated, Modification, Virus

    Single radial immunodiffusion (SRID) assay of goat anti-E7 bHA serum against the H5N2 E7 Ag.

    Journal: Viruses

    Article Title: Development of American-Lineage Influenza H5N2 Reassortant Vaccine Viruses for Pandemic Preparedness

    doi: 10.3390/v11060543

    Figure Lengend Snippet: Single radial immunodiffusion (SRID) assay of goat anti-E7 bHA serum against the H5N2 E7 Ag.

    Article Snippet: Eight plasmids which contained NA and modified HA genes from an H5N2 virus and six internal genes from the Vero-15 virus were transfected into Vero cells to generate H5N2 vaccine viruses by electroporation (Bio-RAD Gene Pulser Xcell system, Hercules, CA, USA).

    Techniques: Radial Immuno Diffusion

    The HI titre of ferret sera after two intramuscular injections of  H5N2  inactivated virus vaccine.

    Journal: Viruses

    Article Title: Development of American-Lineage Influenza H5N2 Reassortant Vaccine Viruses for Pandemic Preparedness

    doi: 10.3390/v11060543

    Figure Lengend Snippet: The HI titre of ferret sera after two intramuscular injections of H5N2 inactivated virus vaccine.

    Article Snippet: Eight plasmids which contained NA and modified HA genes from an H5N2 virus and six internal genes from the Vero-15 virus were transfected into Vero cells to generate H5N2 vaccine viruses by electroporation (Bio-RAD Gene Pulser Xcell system, Hercules, CA, USA).

    Techniques: Virus