Page 401 - Avian Virology: Current Research and Future Trends
P. 401
392 | Vervelde and Kaufman
Kaufman, J. (2018). Generalists and specialists: a new view of how MHC Loudovaris, T., Calnek, B.W., Yoo, B.H., and Fahey, K.J. (1991a). Genetic
class I molecules fight infectious pathogens. Trends Immunol. 39, susceptibility of chicken macrophages to in vitro infection with infectious
367–379. laryngotracheitis virus. Avian Pathol. 20, 291–302.
Kaufman, J., Völk, H., and Wallny, H.J. (1995). A ‘minimal essential Mhc’ Loudovaris, T., Yoo, B.H., and Fahey, K.J. (1991b). Genetic resistance to
and an ‘unrecognized Mhc’: two extremes in selection for polymorphism. infectious laryngotracheitis in inbred lines of White Leghorn chickens.
Immunol. Rev. 143, 63–88. Avian Pathol. 20, 357–361.
Kaufman, J., Milne, S., Göbel, T.W., Walker, B.A., Jacob, J.P., Auffray, C., Luecke, S., and Paludan, S.R. (2017). Molecular requirements for sensing
Zoorob, R., and Beck, S. (1999). The chicken B locus is a minimal of intracellular microbial nucleic acids by the innate immune system.
essential major histocompatibility complex. Nature 401, 923–925. Cytokine 98, 4–14.
https://doi.org/10.1038/44856 Magor, K.E., Miranzo Navarro, D., Barber, M.R., Petkau, K., Fleming-Canepa,
Keestra, A.M., de Zoete, M.R., Bouwman, L.I., Vaezirad, M.M., and van X., Blyth, G.A., and Blaine, A.H. (2013). Defense genes missing from
Putten, J.P. (2013). Unique features of chicken Toll-like receptors. the flight division. Dev. Comp. Immunol. 41, 377–388. https://doi.
Dev. Comp. Immunol. 41, 316–323. https://doi.org/10.1016/j. org/10.1016/j.dci.2013.04.010
dci.2013.04.009 Mándi, Y., Bakay, M., and Béládi, I. (1984). Effect of interferon on antibody-
Kim, T., Hunt, H.D., Parcells, M.S., van Santen, V., and Ewald, S.J. (2018). dependent cellular cytotoxicity (ADCC) in chickens. Acta Microbiol.
Two class I genes of the chicken MHC have different functions: Hung. 31(2), 127–133.
BF1 is recognized by NK cells while BF2 is recognized by CTLs. Masuda, Y., Matsuda, A., Usui, T., Sugai, T., Asano, A., and Yamano, Y.
Immunogenetics 70, 599–611. https://doi.org/10.1007/s00251-018- (2012). Biological effects of chicken type III interferon on expression
1066-2 of interferon-stimulated genes in chickens: comparison with type I and
Kjærup, R.M., Dalgaard, T.S., Norup, L.R., Hamzic, E., Sørensen, P., and type II interferons. J. Vet. Med. Sci. 74, 1381–1386.
Juul-Madsen, H.R. (2014). Characterization of cellular and humoral Mays, J.K., Bacon, L.D., Pandiri, A.R., and Fadly, A.M. (2005). Response
immune responses after IBV infection in chicken lines differing in of white leghorn chickens of various B haplotypes to infection at hatch
MBL serum concentration. Viral Immunol. 27, 529–542. https://doi. with subgroup J avian leukosis virus. Avian Dis. 49, 214–219. https://
org/10.1089/vim.2014.0088 doi.org/10.1637/7315-120104R
Ko, J.H., Takada, A., Mitsuhashi, T., Agui, T., and Watanabe, T. (2004a). Merkle, H., Cihak, J., and Lösch, U. (1992). The cytotoxic T lymphocyte
Native antiviral specificity of chicken Mx protein depends on amino response in reticuloendotheliosis virus-infected chickens is mediated
acid variation at position 631. Anim. Genet. 35, 119–122. https://doi. by alpha beta and not by gamma delta T-cells. Immunobiology 186,
org/10.1111/j.1365-2052.2004.01096.x 292–303.
Ko, J.H., Asano, A., Kon, Y., Watanabe, T., and Agui, T. (2004b). Mesa, C.M., Thulien, K.J., Moon, D.A., Veniamin, S.M., and Magor, K.E.
Characterization of the chicken PKR: polymorphism of the gene and (2004). The dominant MHC class I gene is adjacent to the polymorphic
antiviral activity against vesicular stomatitis virus. Jpn. J. Vet. Res. 51, TAP2 gene in the duck, Anas platyrhynchos. Immunogenetics 56,
123–133. 192–203. https://doi.org/10.1007/s00251-004-0672-3
Kogut, M.H., Iqbal, M., He, H., Philbin, V., Kaiser, P., and Smith, A. (2005). Miller, M.M., and Taylor, R.L. (2016). Brief review of the chicken
Expression and function of toll-like receptors in chicken heterophils. major histocompatibility complex: The genes, their distribution on
Dev. Comp. Immunol. 29, 791–807. chromosome 16, and their contributions to disease resistance. Poult. Sci.
Koyama, S., Ishii, K.J., Coban, C., and Akira, S. (2008). Innate immune 95, 375–392. https://doi.org/10.3382/ps/pev379
response to viral infection. Cytokine 43, 336–341. https://doi. Miller, M.M., Goto, R., Bernot, A., Zoorob, R., Auffray, C., Bumstead, N.,
org/10.1016/j.cyto.2008.07.009 and Briles, W.E. (1994). Two Mhc class I and two Mhc class II genes map
Kumar, P.A., Das, S.K., and Rao, J.R. (1998). Effect of immunostimulation to the chicken Rfp-Y system outside the B complex. Proc. Natl. Acad. Sci.
on cytotoxic activity of intestinal intraepithelial lymphocytes of chickens U.S.A. 91, 4397–4401.
in infectious bursal disease and Eimeria tenella infections. Acta Vet. Miller, M.M., Goto, R.M., Taylor, R.L., Zoorob, R., Auffray, C., Briles,
Hung. 46, 1–11. R.W., Briles, W.E., and Bloom, S.E. (1996). Assignment of Rfp-Y to the
Lakshmanan, N., and Lamont, S.J. (1998). Rfp-Y polymorphism and chicken major histocompatibility complex/NOR microchromosome
Marek’s disease resistance in multitrait immunocompetence-selected and evidence for high-frequency recombination associated with the
chicken lines. Poult. Sci. 77, 538–541. nucleolar organizer region. Proc. Natl. Acad. Sci. U.S.A. 93, 3958–3962.
Lanier, L.L. (2008). Up on the tightrope: natural killer cell activation and Miura, T., Brockman, M.A., Schneidewind, A., Lobritz, M., Pereyra, F.,
inhibition. Nat. Immunol. 9, 495–502. https://doi.org/10.1038/ni1581 Rathod, A., Block, B.L., Brumme, Z.L., Brumme, C.J., Baker, B., et al.
Laun, K., Coggill, P., Palmer, S., Sims, S., Ning, Z., Ragoussis, J., Volpi, (2009). HLA-B57/B*5801 human immunodeficiency virus type 1
E., Wilson, N., Beck, S., Ziegler, A., et al. (2006). The leukocyte elite controllers select for rare gag variants associated with reduced viral
receptor complex in chicken is characterized by massive expansion replication capacity and strong cytotoxic T-lymphocyte recognition. J.
and diversification of immunoglobulin-like Loci. PLOS Genet. 2, e73. Virol. 83, 2743–2755. https://doi.org/10.1128/JVI.02265-08
https://doi.org/10.1371/journal.pgen.0020073 Moon, D.A., Veniamin, S.M., Parks-Dely, J.A., and Magor, K.E. (2005).
Lee, L.F., Bacon, L.D., Yoshida, S., Yanagida, N., Zhang, H.M., and Witter, The MHC of the duck (Anas platyrhynchos) contains five differentially
R.L. (2004). The efficacy of recombinant fowlpox vaccine protection expressed class I genes. J. Immunol. 175, 6702–6712.
against Marek’s disease: its dependence on chicken line and B haplotype. Moretta, A. (2002). Natural killer cells and dendritic cells: rendezvous
Avian Dis. 48, 129–137. in abused tissues. Nat. Rev. Immunol. 2, 957–964. https://doi.
Li, K., Markosyan, R.M., Zheng, Y.M., Golfetto, O., Bungart, B., Li, M., org/10.1038/nri956
Ding, S., He, Y., Liang, C., Lee, J.C., et al. (2013). IFITM proteins restrict Mostafa, A., Abdelwhab, E.M., Mettenleiter, T.C., and Pleschka, S. (2018).
viral membrane hemifusion. PLOS Pathog. 9, e1003124. https://doi. Zoonotic potential of influenza A viruses: A Comprehensive Overview.
org/10.1371/journal.ppat.1003124 Viruses 10, E497.
Liu, G., Wang, Q., Liu, N., Xiao, Y., Tong, T., Liu, S., and Wu, D. (2012). Murphy, K.M., and Weaver, C. (2017). Janeway’s Immunobiology, 9th edn.
Infectious bronchitis virus nucleoprotein specific CTL response is (Garland Science/Taylor & Francis Group, LLC, New York, NY).
generated prior to serum IgG. Vet. Immunol. Immunopathol. 148, Nagarajan, M.M., and Kibenge, F.S. (1997). Infectious bursal disease virus:
353–358. https://doi.org/10.1016/j.vetimm.2012.06.028 a review of molecular basis for variations in antigenicity and virulence.
Lochner, K.M., Viertlboeck, B.C., and Göbel, T.W. (2010). The red jungle Can. J. Vet. Res. 61, 81–88.
fowl leukocyte receptor complex contains a large, highly diverse number Natarajan, K., Dimasi, N., Wang, J., Mariuzza, R.A., and Margulies,
of chicken immunoglobulin-like receptor (CHIR) genes. Mol. Immunol. D.H. (2002). Structure and function of natural killer cell receptors:
47, 1956–1962. https://doi.org/10.1016/j.molimm.2010.05.001 multiple molecular solutions to self, nonself discrimination. Annu.
Rev. Immunol. 20, 853–885. https://doi.org/10.1146/annurev.
immunol.20.100301.064812