Induction profiles of mRNA of toll like receptors and cytokines in chickens pre-exposed to low pathogenic avian influenza H9N2 virus followed by challenge with highly pathogenic avian influenza H5N1 virus

Microb Pathog. 2018 Apr:117:200-205. doi: 10.1016/j.micpath.2018.02.041. Epub 2018 Feb 21.

Abstract

Herein, the induction of TLRs and cytokines in chickens pre-exposed to low pathogenic avian influenza H9N2 virus followed by challenge with highly pathogenic avian influenza (HPAI) H5N1 virus was studied. Four groups (1-4) of chickens inoculated with 106 EID50 of H9N2 virus were challenged with 106 EID50 of H5N1 virus on days 1, 3, 7 and 14 post H9N2 inoculation, respectively. In groups (1-4) TLRs and cytokines induction was studied in chicken PBMCs on day 3 post H5N1 challenge. In H5N1 control group TLRs (1, 2, 5 and 7) cytokines (IFNα, IFNβ, IFNγ, IL1β, IL2, IL4, IL8 and TGF β3) were down regulated. In group 1 down regulation of cytokines and TLRs was similar to H5N1 control birds. Down regulation of TLRs and cytokines in H5N1 control and group 1 resulted death of all the chickens. In group 2, up-regulation of TLRs (3, 7 and 15) and induction of TNFα, IFNα, IFNβ, IFNγ aided virus clearance leading to survival of all the chickens. In group 3 significant up-regulation of TLRs (3, 4 and 15) and significant induction of cytokines (IFNγ, TNFα, IL1β, IL4, IL6, IL8, IL10 and TGF β3) was detected. In group 4 significant up-regulation of TLRs (2, 3, 7 and 15) and significant induction of cytokines (IFNγ, TNFα, IL1β, IL2, IL6, IL8 and IL10) was detected. In groups 3 and 4 simultaneous and significant induction of pro-inflammatory, antiviral and anti-inflammatory cytokine resulted cytokine dysregulation leading to death of (2/6) and (3/6) chickens respectively. Hence, the study revealed TLRs and cytokines role in modulating the H5N1 infection outcome in chickens pre-exposed to H9N2 virus.

Keywords: AIV; Cytokine; Cytokine storm; Down regulation; Fold change; TLR; Up-regulation.

MeSH terms

  • Animals
  • Chickens
  • Cytokines / biosynthesis
  • Cytokines / blood*
  • Disease Models, Animal
  • Down-Regulation
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology*
  • Immunity, Cellular
  • Immunity, Innate
  • Influenza A Virus, H5N1 Subtype / immunology*
  • Influenza A Virus, H5N1 Subtype / pathogenicity
  • Influenza A Virus, H9N2 Subtype / immunology*
  • Influenza A Virus, H9N2 Subtype / pathogenicity
  • Influenza in Birds / immunology*
  • Influenza in Birds / virology
  • RNA, Messenger / metabolism*
  • Toll-Like Receptors / blood*
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / metabolism
  • Up-Regulation

Substances

  • Cytokines
  • RNA, Messenger
  • Toll-Like Receptors