h5n2 viruses (ATCC)
Structured Review

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
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
Figure Legend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-28/2018 (A/H5N2) genome.
Techniques Used: Sequencing
Figure Legend Snippet: Sequence homology of the whole A/Bean Goose/South Korea/KNU18-86/2018 (A/H5N2) genome.
Techniques Used: Sequencing
Figure Legend Snippet: Sequence homology of the whole A/Wild duck/South Korea/KNU18-93/2018 (A/H5N2) genome.
Techniques Used: Sequencing
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:
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
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:
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
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
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
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
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
