CpG oligodeoxynucleotide and double-stranded RNA synergize inflammatory cytokine gene expressions in chicken monocytes (90.13)
Haiqi He, Kenneth J. Genovese, Michael H. Kogut
Abstract
Haiqi He, Kenneth J. Genovese, Michael H. Kogut
Abstract
Abstract Toll-like receptors (TLRs) recognize microbial components and initiate innate immune responses that control microbial infections. We have investigated the innate immune response of chicken monocytes to CpG-motif containing oligodeoxydinucleotide, CpG-ODN, and the analog of viral double-stranded RNA, poly I:C. Our results show ligands poly I:C and CpG-ODN of the TLR3 and TLR9, respectively, synergized the induction of many genes involving inflammatory responses including nitric oxide and cytokines, IL-1β, IFN-α, IFN-β, IFN-γ, IL-18, and IL-12, in chicken monocytes. We also demonstrated the differential responses of some cytokines such as IL-18 and IFN-β to CpG-ODN and poly I:C stimulations, respectively. Those results demonstrate differential roles for TLR3 and TLR9 in signaling immune responses to bacterial and viral infections in chicken monocytes as well as a synergistic interaction between the two signaling pathways. Furthermore, our results suggest synergistic interaction between TLR3 and TLR9 pathways may contribute the “lethal synergism” from bacterial and viral co-infections.
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Abstract Toll-like receptors (TLRs) recognize microbial components and initiate innate immune responses that control microbial infections. We have investigated the innate immune response of chicken monocytes to CpG-motif containing oligodeoxydinucleotide, CpG-ODN, and the analog of viral double-stranded RNA, poly I:C. Our results show ligands poly I:C and CpG-ODN of the TLR3 and TLR9, respectively, synergized the induction of many genes involving inflammatory responses including nitric oxide and cytokines, IL-1β, IFN-α, IFN-β, IFN-γ, IL-18, and IL-12, in chicken monocytes. We also demonstrated the differential responses of some cytokines such as IL-18 and IFN-β to CpG-ODN and poly I:C stimulations, respectively. Those results demonstrate differential roles for TLR3 and TLR9 in signaling immune responses to bacterial and viral infections in chicken monocytes as well as a synergistic interaction between the two signaling pathways. Furthermore, our results suggest synergistic interaction between TLR3 and TLR9 pathways may contribute the “lethal synergism” from bacterial and viral co-infections.
Key concepts: TLR9, TLR3, CpG Oligodeoxynucleotide, Innate immune system, TLR7, CpG site, Immune system, Biology