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PAIVS: prediction of avian influenza virus subtype

  • Park, Hyeon-Chun (Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea) ;
  • Shin, Juyoun (Department of Microbiology, College of Medicine, The Catholic University of Korea) ;
  • Cho, Sung-Min (Integrated Research Center for Genome Polymorphism, College of Medicine, The Catholic University of Korea) ;
  • Kang, Shinseok (Chungbuk Veterinary Service Laboratory) ;
  • Chung, Yeun-Jun (Department of Microbiology, College of Medicine, The Catholic University of Korea) ;
  • Jung, Seung-Hyun (Cancer Evolution Research Center, College of Medicine, The Catholic University of Korea)
  • Received : 2020.01.09
  • Accepted : 2020.02.11
  • Published : 2020.03.31

Abstract

Highly pathogenic avian influenza (HPAI) viruses have caused severe respiratory disease and death in poultry and human beings. Although most of the avian influenza viruses (AIVs) are of low pathogenicity and cause mild infections in birds, some subtypes including hemagglutinin H5 and H7 subtype cause HPAI. Therefore, sensitive and accurate subtyping of AIV is important to prepare and prevent for the spread of HPAI. Next-generation sequencing (NGS) can analyze the full-length sequence information of entire AIV genome at once, so this technology is becoming a more common in detecting AIVs and predicting subtypes. However, an analysis pipeline of NGS-based AIV sequencing data, including AIV subtyping, has not yet been established. Here, in order to support the pre-processing of NGS data and its interpretation, we developed a user-friendly tool, named prediction of avian influenza virus subtype (PAIVS). PAIVS has multiple functions that support the pre-processing of NGS data, reference-guided AIV subtyping, de novo assembly, variant calling and identifying the closest full-length sequences by BLAST, and provide the graphical summary to the end users.

Keywords

References

  1. Capua I, Alexander DJ. Avian influenza and human health. Acta Trop 2002;83:1-6. https://doi.org/10.1016/S0001-706X(02)00050-5
  2. Tong S, Zhu X, Li Y, Shi M, Zhang J, Bourgeois M, et al. New world bats harbor diverse influenza A viruses. PLoS Pathog 2013;9:e1003657. https://doi.org/10.1371/journal.ppat.1003657
  3. Claes F, Morzaria SP, Donis RO. Emergence and dissemination of clade 2.3.4.4 H5Nx influenza viruses: how is the Asian HPAI H5 lineage maintained. Curr Opin Virol 2016;16:158-163. https://doi.org/10.1016/j.coviro.2016.02.005
  4. Pantin-Jackwood MJ, Costa-Hurtado M, Shepherd E, DeJesus E, Smith D, Spackman E, et al. Pathogenicity and transmission of H5 and H7 highly pathogenic Avian influenza viruses in mallards. J Virol 2016;90:9967-9982. https://doi.org/10.1128/JVI.01165-16
  5. Vemula SV, Zhao J, Liu J, Wang X, Biswas S, Hewlett I. Current approaches for diagnosis of influenza virus infections in humans. Viruses 2016;8:96. https://doi.org/10.3390/v8040096
  6. Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 2014;30:2114-2120. https://doi.org/10.1093/bioinformatics/btu170
  7. Kim D, Langmead B, Salzberg S. HISAT2: graph-based alignment of next-generation sequencing reads to a population of genomes. Baltimore, MD: Johns Hopkins University, Center for Computational Biology, 2017. Accessed 2019 Dec 10. Available from: https://ccb.jhu.edu/software/hisat2/manual.shtml.
  8. Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009;25:1754-1760. https://doi.org/10.1093/bioinformatics/btp324
  9. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 2009;25:2078-2079. https://doi.org/10.1093/bioinformatics/btp352
  10. Danecek P, McCarthy SA. BCFtools/csq: haplotype-aware variant consequences. Bioinformatics 2017;33:2037-2039. https://doi.org/10.1093/bioinformatics/btx100
  11. Koboldt DC, Zhang Q, Larson DE, Shen D, McLellan MD, Lin L, et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 2012;22:568-576. https://doi.org/10.1101/gr.129684.111
  12. McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 2010;20:1297-1303. https://doi.org/10.1101/gr.107524.110
  13. Hunt M, Gall A, Ong SH, Brener J, Ferns B, Goulder P, et al. IVA: accurate de novo assembly of RNA virus genomes. Bioinformatics 2015;31:2374-2376. https://doi.org/10.1093/bioinformatics/btv120
  14. Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, et al. BLAST+: architecture and applications. BMC Bioinformatics 2009;10:421. https://doi.org/10.1186/1471-2105-10-421