| Literature DB >> 33550926 |
Beate M Crossley1, Daniel Rejmanek1, John Baroch2, James B Stanton3, Kelsey T Young3, Mary Lea Killian4, Mia K Torchetti4, Sharon K Hietala1.
Abstract
We report whole-genome sequencing of influenza A virus (IAV) with 100% diagnostic sensitivity and results available in <24-48 h using amplicon-based nanopore sequencing technology (MinION) on clinical material from wild waterfowl (n = 19), commercial poultry (n = 4), and swine (n = 3). All 8 gene segments of IAV including those from 14 of the 18 recognized hemagglutinin subtypes and 9 of the 11 neuraminidase subtypes were amplified in their entirety at >500× coverage from each of 16 reference virus isolates evaluated. Subgenomic viral sequences obtained in 3 cases using Sanger sequencing as the reference standard were identical to those obtained when sequenced using the MinION approach. An inter-laboratory comparison demonstrated reproducibility when comparing 2 independent laboratories at ≥99.8% across the entirety of the IAV genomes sequenced.Entities:
Keywords: MinION; avian influenza A virus; nanopore; whole-genome sequencing
Mesh:
Year: 2021 PMID: 33550926 PMCID: PMC7953088 DOI: 10.1177/1040638720984114
Source DB: PubMed Journal: J Vet Diagn Invest ISSN: 1040-6387 Impact factor: 1.279