Page 398 - Avian Virology: Current Research and Future Trends
P. 398

Avian Immune Responses to Virus Infection |   389
                                                                Aoshi, T., Koyama, S., Kobiyama, K., Akira, S., and Ishii, K.J. (2011). Innate
          Future prospects                                        and adaptive immune responses to viral infection and vaccination. Curr.
          Already it is clear that there are aspects of innate and adaptive   Opin. Virol. 1, 226–232. https://doi.org/10.1016/j.coviro.2011.07.002
          responses in birds that are different from those in mammals.   Ariaans, M.P., van de Haar, P.M., Hensen, E.J., and Vervelde, L. (2009).
          Examples include the differences in key interferon, cytokine   Infectious bronchitis virus induces acute interferon-gamma production
          and chemokine genes, and the expression of single dominantly   through polyclonal stimulation of chicken leukocytes. Virology  385,
                                                                  68–73. https://doi.org/10.1016/j.virol.2008.11.021
          expressed MHC molecules that can determine the success of the   Bacon, L.D. (1987). Influence of the major histocompatibility complex on
          immune response and thus lead to strong genetic associations of   disease resistance and productivity. Poult. Sci. 66, 802–811. https://doi.
          the MHC with infectious diseases.                       org/10.3382/ps.0660802
            The genetic bases for some innate immune responses in birds   Bacon, L.D., and R.L. Witter. (1994). Serotype specificity of B-haplotype
          have described, but there are presumably many other innate pro-  influence on the relative efficacy of Marek’s disease vaccines. Avian Dis.
                                                                  38, 65–71.
          cesses to be discovered. Moreover, there is much to be learned   Bacon, L.D., Witter, R.L., Crittenden, L.B., Fadly, A., and Motta, J. (1981).
          about the mechanisms of resistance and susceptibility deter-  B-haplotype influence on Marek’s disease, Rous sarcoma, and lymphoid
                                                                  leukosis virus-induced tumors in chickens. Poult. Sci. 60, 1132–1139.
          mined by different innate immunity genes, including the actions   Bacon, L.D., Hunt, H.D., and Cheng, H.H. (2000). A review of the
          of many PRRs (including TLRs, NLRs, RIRs, scavenger recep-  development of  chicken lines to  resolve genes determining  resistance
          tors and lectins), cytokines (including the interferon systems)   to diseases. Poult. Sci.  79, 1082–1093. https://doi.org/10.1093/
          and chemokines, and NK cells, receptors and ligands.    ps/79.8.1082
            Similarly, much is now understood about how the MHC class   Bacon, L.D., Hunter, D.B., Zhang, H.M., Brand, K., and Etches, R. (2004).
          I system of chickens works, but there is much more to be learned   Retrospective  evidence  that  the  MHC  (B  haplotype)  of  chickens
                                                                  influences genetic resistance to attenuated infectious bronchitis vaccine
          about the MHC class II system, antigen processing and peptide   strains in chickens. Avian Pathol. 33, 605–609.
          loading in the various APCs, the location of the initiation of the   Balachandran, S., Roberts, P.C., Brown, L.E., Truong, H., Pattnaik,
          adaptive immune response, the TCR repertoire and the different   A.K., Archer, D.R., and Barber, G.N. (2000). Essential role for the
                                                                  dsRNA-dependent protein kinase PKR in innate immunity to viral
          T-cell subsets (both αβ and γδ, and the different T helper cell   infection. Immunity 13, 129–141.
          subsets), the antibody V region repertoire, affinity maturation   Balakrishnan, C.N., Ekblom, R., Völker, M., Westerdahl, H., Godinez, R.,
          and isotype switching.                                  Kotkiewicz, H., Burt, D.W., Graves, T., Griffin, D.K., Warren, W.C.,
            Such knowledge should allow better breeding for resistance   et al.  (2010).  Gene  duplication  and  fragmentation  in  the  zebra  finch
          phenotypes, as well as development of improved vaccines that   major  histocompatibility complex. BMC  Biol.  8, 29.  https://doi.
                                                                  org/10.1186/1741-7007-8-29
          deliver the right response at the right time and in the right place.   Banat, G.R., Tkalcic, S., Dzielawa, J.A., Jackwood, M.W., Saggese, M.D., Yates,
          Moreover, such knowledge forms the basis for research into birds   L., Kopulos, R., Briles, W.E., and Collisson, E.W. (2013). Association of
          that are not commercial livestock.                      the chicken MHC B haplotypes with resistance to avian coronavirus.
                                                                  Dev. Comp. Immunol.  39, 430–437. https://doi.org/10.1016/j.
                                                                  dci.2012.10.006
          References                                            Barrow, A.D., Burgess, S.C., Baigent, S.J., Howes, K., and Nair, V.K. (2003).
          Abbas, A.K., Lichtman, A.H, and Pillai, S. (2016). Basic immunology:   Infection of macrophages by a lymphotropic herpesvirus: a new tropism
            functions and disorders of the immune system, fifth edn. (Elsevier, St.   for Marek’s disease virus. J. Gen. Virol. 84, 2635–2645.
            Louis, MO).                                         Bassano, I., Ong, S.H., Lawless, N., Whitehead, T., Fife, M., and Kellam,
          Abdul-Careem, M.F., Haq, K., Shanmuganathan, S., Read, L.R., Schat, K.A.,   P. (2017). Accurate characterization of the IFITM locus using MiSeq
            Heidari, M., and Sharif, S. (2009). Induction of innate host responses   and PacBio sequencing shows genetic variation in Galliformes. BMC
            in the lungs of chickens following infection with a very virulent   Genomics 18, 419. https://doi.org/10.1186/s12864-017-3801-8
            strain  of  Marek’s  disease  virus.  Virology  393,  250–257.  https://doi.  Bazzigher, L., Schwarz, A., and Staeheli, P. (1993). No enhanced influenza
            org/10.1016/j.virol.2009.08.001                       virus resistance of murine and avian cells expressing cloned duck Mx
          Adams, S.C., Xing, Z., Li, J., and Cardona, C.J. (2009). Immune-related   protein. Virology 195, 100–112.
            gene expression in response to H11N9 low pathogenic avian influenza   Beachboard, D.C., and Horner, S.M. (2016). Innate immune evasion
            virus infection in chicken and Pekin duck peripheral blood mononuclear   strategies of DNA and RNA viruses. Curr. Opin. Microbiol. 32, 113–119.
            cells. Mol. Immunol.  46, 1744–1749. https://doi.org/10.1016/j.  Benfield, C.T., Lyall, J.W., and Tiley, L.S., (2010). The cytoplasmic location
            molimm.2009.01.025                                    of chicken mx is not the determining factor for its lack of antiviral activity.
          Afanassieff, M., Goto, R.M., Ha, J., Sherman, M.A., Zhong, L., Auffray, C.,   PLOS ONE 5, e12151.
            Coudert, F., Zoorob, R., and Miller, M.M. (2001). At least one class I   Biron, C.A., Nguyen, K.B., Pien, G.C., Cousens, L.P., and Salazar-Mather, T.P.
            gene in restriction fragment pattern-Y (Rfp-Y), the second MHC gene   (1999). Natural killer cells in antiviral defense: function and regulation
            cluster in the chicken, is transcribed, polymorphic, and shows divergent   by innate cytokines. Annu. Rev. Immunol.  17, 189–220. https://doi.
            specialization in antigen binding region. J. Immunol. 166, 3324–3333.  org/10.1146/annurev.immunol.17.1.189
          Afonso, C.L., Tulman, E.R., Lu, Z., Zsak, L., Kutish, G.F., and Rock, D.L.   Blyth, G.A., Chan, W.F., Webster, R.G., and Magor, K.E. (2016). Duck
            (2000). The genome of fowlpox virus. J. Virol. 74, 3815–3831.  interferon-inducible transmembrane protein 3 Mediates restriction
          Akira, S., Uematsu, S., and Takeuchi, O. (2006). Pathogen recognition and   of  influenza  viruses.  J. Virol.  90, 103–116.  https://doi.org/10.1128/
            innate immunity. Cell 124, 783–801.                   JVI.01593-15
          Alcaide, M., Liu, M., and Edwards, S.V. (2013). Major histocompatibility   Boonyanuwat, K., Thummabutra, S., Sookmanee, N., Vatchavalkhu, V.,
            complex class I evolution in songbirds: universal primers, rapid evolution   and Siripholvat, V. (2006). Influences of major histocompatibility
            and base compositional shifts in exon 3. PeerJ  1, e86. https://doi.  complex class I haplotypes on avian influenza virus disease traits in Thai
            org/10.7717/peerj.86                                  indigenous chickens. Anim. Sci. J. 77, 285–289.
          Altfeld, M., Fadda, L., Frleta, D., and Bhardwaj, N. (2011). DCs and NK cells:   BoseDasgupta, S., and Pieters, J. (2014). Inflammatory stimuli reprogram
            critical effectors in the immune response to HIV-1. Nat. Rev. Immunol.   macrophage phagocytosis to macropinocytosis for the rapid elimination
            11, 176–186. https://doi.org/10.1038/nri2935          of pathogens. PLOS Pathog.  10, e1003879. https://doi.org/10.1371/
                                                                  journal.ppat.1003879
   393   394   395   396   397   398   399   400   401   402   403