tetano
Editor, Senior Moderator
J Virol Methods
. 2023 Jul 17;320:114773.
doi: 10.1016/j.jviromet.2023.114773. Online ahead of print. Subtype specific virus enrichement with immunomagnetic separation method followed by NGS unravels the mixture of H5 and H9 avian influenza virus
Eun Bi Noh[SUP] 1 [/SUP], Gyeong-Beom Heo[SUP] 2 [/SUP], Kwang-Nyeong Lee[SUP] 3 [/SUP], Yong-Myung Kang[SUP] 4 [/SUP], Se-Hee An[SUP] 5 [/SUP], Nayeong Kim[SUP] 6 [/SUP], Youn-Jeong Lee[SUP] 7 [/SUP]
Affiliations
Wild bird avian influenza type A virus (AIV) surveillance is important for the early detection of highly pathogenic AIVs and for providing early warnings to the poultry industry and veterinary services to implement more effective control measures against these viruses. Some field samples are often found to contain more than two kinds of AIV. Correct determination of the HA/NA subtype and complete nucleotide sequences of the component viruses in those samples are often critical for timely and accurate understanding of the field situation, but it is not easy to define the genomic structure of the constituent viruses unambiguously because AIV has eight segmented genomes. In this study, with immunomagnetic beads incorporating polyclonal antibodies of chicken for subtype-specific viral enrichment, we could selectively decrease the density of one of the two constituent viruses in a sample of different subtypes, H5 and H9, artificially generated; this was represented in the changes of Ct values with subtype specific real-time RT-PCR. Following this, with NGS, we could recover nearly complete genomic sequences and arrange the consensus sequences of gene segments of the constituent viruses confidently with the quantitative variable like genome coverage, linked along the gene segments and associated with the number of viral copies in a sample.
Keywords: Avian influenza virus; Detection; Enrichment; Fecal sample; Immunomagnetic separation; NGS.
. 2023 Jul 17;320:114773.
doi: 10.1016/j.jviromet.2023.114773. Online ahead of print. Subtype specific virus enrichement with immunomagnetic separation method followed by NGS unravels the mixture of H5 and H9 avian influenza virus
Eun Bi Noh[SUP] 1 [/SUP], Gyeong-Beom Heo[SUP] 2 [/SUP], Kwang-Nyeong Lee[SUP] 3 [/SUP], Yong-Myung Kang[SUP] 4 [/SUP], Se-Hee An[SUP] 5 [/SUP], Nayeong Kim[SUP] 6 [/SUP], Youn-Jeong Lee[SUP] 7 [/SUP]
Affiliations
- PMID: 37467847
- DOI: 10.1016/j.jviromet.2023.114773
Wild bird avian influenza type A virus (AIV) surveillance is important for the early detection of highly pathogenic AIVs and for providing early warnings to the poultry industry and veterinary services to implement more effective control measures against these viruses. Some field samples are often found to contain more than two kinds of AIV. Correct determination of the HA/NA subtype and complete nucleotide sequences of the component viruses in those samples are often critical for timely and accurate understanding of the field situation, but it is not easy to define the genomic structure of the constituent viruses unambiguously because AIV has eight segmented genomes. In this study, with immunomagnetic beads incorporating polyclonal antibodies of chicken for subtype-specific viral enrichment, we could selectively decrease the density of one of the two constituent viruses in a sample of different subtypes, H5 and H9, artificially generated; this was represented in the changes of Ct values with subtype specific real-time RT-PCR. Following this, with NGS, we could recover nearly complete genomic sequences and arrange the consensus sequences of gene segments of the constituent viruses confidently with the quantitative variable like genome coverage, linked along the gene segments and associated with the number of viral copies in a sample.
Keywords: Avian influenza virus; Detection; Enrichment; Fecal sample; Immunomagnetic separation; NGS.