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http://dx.doi.org/10.5713/ajas.2009.80338

Lower Antibody Response in Chickens Homozygous for the Mx Resistant Allele to Avian Influenza  

Qu, L.J. (State Laboratory for Agrobiotechnology and Department of Animal Science and Technology, China Agricultural University)
Li, X.Y. (State Laboratory for Agrobiotechnology and Department of Animal Science and Technology, China Agricultural University)
Xu, G.Y. (State Laboratory for Agrobiotechnology and Department of Animal Science and Technology, China Agricultural University)
Ning, Z.H. (State Laboratory for Agrobiotechnology and Department of Animal Science and Technology, China Agricultural University)
Yang, N. (State Laboratory for Agrobiotechnology and Department of Animal Science and Technology, China Agricultural University)
Publication Information
Asian-Australasian Journal of Animal Sciences / v.22, no.4, 2009 , pp. 465-470 More about this Journal
Abstract
The chicken Mx gene has been regarded as a candidate gene for resistance to avian influenza virus (AIV). In this study, three groups of chickens with homozygotes (AA, GG) and heterozygotes (AG) of the resistant (A) and susceptible alleles (G) to AIV of the Mx gene were constructed from a line of dwarf egg-type chickens. These chickens were not examined for their resistant activities to AIV because the differential resistance had only been detected in vitro. The birds of the three groups were vaccinated with inactivated H5N2 AIV vaccine and the level of hemagglutination inhibition (HI) antibody to AIV was detected. The association between disease resistant activity to AIV and antibody response to AIV vaccination in the three groups was analyzed. The chickens with homozygous resistant allele A showed the lowest antibody levels, whereas the heterozygous chickens (AG) presented the highest antibody level after the boosting vaccination, which indicates that the efficiency of artificial selection on the resistant allele of Mx gene will be compromised since the homozygotes of the allele presented the weakest antibody response to the corresponding vaccine.
Keywords
Antibody Response; Disease Resistance; Chick; Mx Gene; Avian Influenza;
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1 Beuken, E., G. Grauls, C. A. Bruggeman and C. Vink. 1999. The rat cytomegalovirus R32 gene encodes a virion-associated protein that elicits a strong humoral immune response in infected rats. J. Gen. Virol. 80 (Pt 10):2719-2728
2 Bucin, D., T. Lindholm and N. H. Persson. 1992. HLA-A region in highly sensitized patients: another immune response gene region. Exp. Clin. Immunogenet. 9:154-160   DOI   PUBMED
3 Haller, O., M. Frese and G. Kochs. 1998. Mx proteins: mediators of innate resistance to RNA viruses. Rev. Sci. Tech. 17:220-230
4 Hou, Z. C., G. Y. Xu and Z. Su. 2007. Purifying selection and positive selection on the myxovirus resistance gene in mammals and chickens. Gene. 396:188-195
5 Jansa, S. A., B. L. Lundrigan and P. K. Tucker. 2003. Tests for positive selection on immune and reproductive genes in closely related species of the murine genus mus. J. Mol. Evol. 56:294-307   DOI   ScienceOn
6 Quere, P., C. Rivas, K. Ester, K., Novak and W. L. Ragland. 2005. Abundance of IFN-alpha and IFN-gamma mRNA in blood of resistant and susceptible chickens infected with Marek's disease virus (MDV) or vaccinated with turkey herpesvirus; and MDV inhibition of subsequent induction of IFN gene transcription. Arch. Virol. 150:507-519   DOI   ScienceOn
7 Staeheli, P., Y. X. Yu, R. Grob and O. Haller. 1989. A doublestranded RNA-inducible fish gene homologous to the murine influenza virus resistance gene Mx. Mol. Cell Biol. 9:3117-3121   DOI   PUBMED   ScienceOn
8 Wang, E. T., G. Kodama, P. Baldi and R. K. Moyzis. 2006. Global landscape of recent inferred Darwinian selection for Homo sapiens. Proc. Natl. Acad. Sci. 103:135-140   DOI   ScienceOn
9 Berlin, S., L. Qu, X. Li, N. Yang and H. Ellegren. 2008. Positive diversifying selection in avian Mx genes. Immunogenetics 60:689-697   DOI   ScienceOn
10 Pavlovic, J. and P. Staeheli. 1991. The antiviral potentials of Mx proteins. J. Interferon Res. 11:215-219   DOI   PUBMED   ScienceOn
11 Weigend, S., N. Mielenz and S. J. Lamont. 1997. Application of a nonlinear regression function to evaluate the kinetics of antibody response to vaccines in chicken lines divergently selected for multitrait immune response. Poult. Sci. 76:1248-1255   PUBMED
12 O'Connell, M. J. and J. O. McInerney. 2005. Gamma chain receptor interleukins: evidence for positive selection driving the evolution of cell-to-cell communicators in the mammalian immune system. J. Mol. Evol. 61:608-619   DOI   ScienceOn
13 Steadham, E. M., S. J. Lamont, I. Kujdych and A. W. Nordskog. 1987. Association of Marek's disease with Ea-B and immune response genes in subline and F2 populations of the Iowa State S1 Leghorn line. Poult. Sci. 66:571-575   DOI   PUBMED   ScienceOn
14 An, B. K., B. L. Cho, S. J. You, H. D. Paik, H. I. Chang, S. W. Kim, C. W. Yun and C. W. Kang. 2008. Growth performance and antibody response of broiler chicks fed yeast derived $\beta$-glucan and single-strain probiotics. Asian-Aust. J. Anim. Sci. 21:1027-1032
15 Plant, K. P. and R. L. Thune. 2004. Cloning and characterisation of a channel catfish (Ictalurus punctatus) Mx gene. Fish Shellfish Immunol. 16:391-405   DOI   ScienceOn
16 Arnheiter, H. and O. Haller. 1983. Mx gene control of interferon action: different kinetics of the antiviral state against influenza virus and vesicular stomatitis virus. J. Virol. 47:626-630
17 Bernasconi, D., U. Schultz and P. Staeheli. 1995. The interferoninduced Mx protein of chickens lacks antiviral activity. J. Interferon Cytokine Res. 15:47-53   DOI   ScienceOn
18 Siegel, P. B. and W. B. Gross. 1980. Production and persistence of antibodies in chicken to sheep erythrocytes, 1. Directional selection. Poult. Sci. 59:1-5   DOI
19 Li, X. Y., L. J. Qu, J. F. Yao, L. J. Qu, J. F. Yao and N. Yang. 2006. Skewed allele frequencies of an Mx gene mutation with potential resistance to avian influenza virus in different chicken populations. Poult. Sci. 85:1327-1329   PUBMED
20 SAS_Institute., Version 8.2. Cary. 2001
21 Bazzigher, L., A. Schwarz and P. Staeheli. 1993. No enhanced influenza virus resistance of murine and avian cells expressing cloned duck Mx protein. Virol. 195:100-112   DOI   ScienceOn
22 Biozzi, G., D. Mouton, O. A. Sant'Anna, H. C. Passos, M. Gennari, M. H. Reis, V. C. Ferreira, A. M. Heumann, Y. Bouthillier, O. M. Ibanez, C. Stiffel and M. Siqueira. 1979. Genetics of immunoresponsiveness to natural antigens in the mouse. Curr. Top Microbiol. Immunol. 85:31-98   PUBMED
23 Pevzner, I. Y., I. Kujdych and A. W. Nordskog. 1981a. Immune response and disease resistance in chickens. II. Marek's disease and immune response to GAT. Poult. Sci. 60:927-932   DOI   PUBMED   ScienceOn
24 Rothman, J. H., C. K. Raymond, T. Gilbert, P. J. O'Hara and T. H. Stevens. 1990. A putative GTP binding protein homologous to interferon-inducible Mx proteins performs an essential function in yeast protein sorting. Cell 61:1063-1074   DOI   ScienceOn
25 Ko, J. H., H. K. Jin, A. Asano, A. Takada, A. Ninomiya, H. Kida, H. Hokiyama, M. Ohara, M. Tsuzuki, M. Nishibori, M. Mizutani and T. Watanabe. 2002. Polymorphisms and the differential antiviral activity of the chicken Mx gene. Genome Res. 12:595-601   PUBMED
26 Dalgaard, T. S., S. Hojsgaard, K. Skjodt and H. R. Juul-Madsen. 2003. Differences in chicken major histocompatibility complex (MHC) class Ialpha gene expression between Marek's diseaseresistant and -susceptible MHC haplotypes. Scand. J. Immunol. 57:135-143
27 Pevzner, I. Y., H. A. Stone and A. W. Nordskog. 1981b. Immune response and disease resistance in chickens. I. Selection for high and low titer to Salmonella pullorum antigen. Poult. Sci. 60:920-926   DOI   PUBMED   ScienceOn
28 Flex, A., E. Gaetani, R. Pola, R. Santoliquido, F. Aloi, P. Papaleo, A. Dal Lago, E. Pola, M. Serricchio, P. Tondi and P. Pola. 2002. The -174 G/C polymorphism of the interleukin-6 gene promoter is associated with peripheral artery occlusive disease. Eur. J. Vasc. Endovasc. Surg. 24:264-268   DOI   ScienceOn
29 Ko, J. H., A. Takada, T. Mitsuhashi, T. Agui and T. Watanabe. 2004. Native antiviral specificity of chicken Mx protein depends on amino acid variation at position 631. Anim. Genet. 35:119-122   DOI   ScienceOn
30 Staeheli, P. 1990. Interferon-induced proteins and the antiviral state. Adv. Virus Res. 38:147-200   DOI   PUBMED   ScienceOn
31 Vallender, E. J. and B. T. Lahn. 2004. Positive selection on the human genome. Hum. Mol. Genet. 13 Spec. No 2:R245-254   DOI   ScienceOn
32 Flohr, F., S. Schneider-Schaulies, O. Haller and G. Kochs. 1999. The central interactive region of human MxA GTPase is involved in GTPase activation and interaction with viral target structures. FEBS Lett. 463:24-28   DOI   ScienceOn
33 Lee, S. H. and S. M. 2002. Vidal. Functional diversity of Mx proteins: variations on a theme of host resistance to infection. Genome Res. 12:527-530   DOI   ScienceOn
34 Leitner, G., Z. Uni, A. Cahaner, M. Gutman and E. D. Heller. 1992. Replicated divergent selection of broiler chickens for high or low early antibody response to Escherichia coli vaccination. Poult. Sci. 71:27-37   DOI   PUBMED   ScienceOn
35 McMichael, A. and J. Bell. 1991. HLA B27: a disease-associated immune response gene. Res. Immunol. 142:475-482   DOI   ScienceOn
36 Rund, D., I. Azar and O. Shperling. 1999. A mutation in the promoter of the multidrug resistance gene (MDR1) in human hematological malignancies may contribute to the pathogenesis of resistant disease. Adv. Exp. Med. Biol. 457:71-75   PUBMED
37 van der Zijpp, A. J., K. Frankena and J. Boneschanscher. 1983. Genetic analysis of primary and secondary immune responses in the chicken. Poult. Sci. 62:565-572   DOI   PUBMED   ScienceOn