Comparative moleculo-immunological analysis of swamp- and riverine-type water buffaloes responses

Cytokine

Volumn 46, Issue 2, 2009, Pages 273-282

  Mingala, Claro N ^a,b   Konnai, Satoru ^a   Cruz, Libertado C ^b   Onuma, Misao ^a   Ohashi, Kazuhiko ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b Philippine Carabao Center National Headquarters and Genepool   (Philippines)

Author keywords

A. marginale; BLV; BVDV; Cytokines; Promoter region

Indexed keywords

CONCANAVALIN A; CYTOKINE; GAMMA INTERFERON; INTERLEUKIN 10; INTERLEUKIN 12P40; INTERLEUKIN 2; INTERLEUKIN 4; LUCIFERASE; TUMOR NECROSIS FACTOR ALPHA;

ANAPLASMA MARGINALE; ANAPLASMOSIS; ARTICLE; BABESIA BIGEMINA; BABESIOSIS; BLOOD SAMPLING; BOVINE DIARRHEA VIRUS; BOVINE LEUKEMIA VIRUS; BUFFALO; COMPARATIVE STUDY; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DNA POLYMORPHISM; DOWN REGULATION; GENETIC TRANSCRIPTION; IMMUNE RESPONSE; IMMUNOLOGICAL PROCEDURES; NONHUMAN; PATHOGENESIS; PERIPHERAL BLOOD MONONUCLEAR CELL; PHILIPPINES; PREVALENCE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; REAL TIME POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM; UPREGULATION;

ANAPLASMA MARGINALE; ANAPLASMOSIS; ANIMALS; BABESIA; BABESIOSIS; BASE SEQUENCE; BUFFALOES; CATTLE; CYTOKINES; DIARRHEA VIRUSES, BOVINE VIRAL; ENVIRONMENT; ENZOOTIC BOVINE LEUKOSIS; FRESH WATER; INTERFERON-GAMMA; INTERLEUKINS; LEUKEMIA VIRUS, BOVINE; MOLECULAR SEQUENCE DATA; PESTIVIRUS INFECTIONS; POLYMORPHISM, GENETIC; PROMOTER REGIONS, GENETIC; SEQUENCE ALIGNMENT; TRANSCRIPTION, GENETIC; TUMOR NECROSIS FACTOR-ALPHA;

ANAPLASMA MARGINALE; ANIMALIA; BABESIA BIGEMINA; BOVINE LEUKEMIA VIRUS; BOVINE VIRAL DIARRHEA VIRUS 1; BUBALUS; BUBALUS CARABANENSIS;

EID: 67349114864     PISSN: 10434666     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cyto.2009.02.006     Document Type: Article

References (67)

1. Ligda DJ. The water buffalo. Web edit 1996. Available from: http://www.netnitco.net/users/djligda/waterbuf.htm.
2. Parker BA. Genetic improvement. In: Ranjhan S.K., and Faylon P.S. (Eds). Carabao production in the Philippines (1992), PCARRD and FAO/UNDP 50-58
3. Frisch J.E., and Vercoe J.E. Adaptive and productive features of cattle growth in the tropics: their relevance to buffalo production. Trop Anim Prod 4 (1979) 3
4. Hung N.H. Survey on blood-parasite diseases of buffalo and cattle of industrial and rural farms in the southern provinces of Vietnam. Proc Res Anim Husbandry Vet Med vol. 1 (1985), Faculty of Animal Husbandry and Veterinary Medicine of University of Cantho 9 Vietnamese
5. National Workshop on Swamp Buffalo Development (NWSBD). Recommendations 2001. Available from: http://www.mekarn.org/procbuf/recom.htm.
6. Burny A., Willems L., Callebaut I., Adam E., Cludts I., Dequiedt F., et al. Bovine leukemia virus: biology and mode of transformation. In: Minson A.C., Neil J.C., and McRae M.A. (Eds). Viruses and cancer (1994), Cambridge University Press, Cambridge 313-334
7. Burny A., Cleuter Y., Kettmann R., Mammerickx M., Marbaix G., Portetelle D., et al. Bovine leukaemia: facts and hypotheses derived from the study of an infectious cancer. Vet Microbiol 17 (1988) 197-218
8. Mirsky M.L., Olmstead C.A., Da Y., and Lewin H.A. The prevalence of proviral bovine leukemia virus in peripheral blood mononuclear cells at two subclinical stages of infection. J Virol 70 (1996) 2178-2183
9. Baker J.C. The clinical manifestations of bovine viral diarrhea infection. Vet Clin North Am Food Anim Pract 11 (1995) 425-445
10. Brock K.V. The persistence of bovine viral diarrhea virus. Biologicals 31 (2003) 133-135
11. Houe H. Epidemiological features and economical importance of bovine viral diarrhoea virus (BVDV) infections. Vet Microbiol 64 (1999) 89-107
12. Carman S., van Dreumel T., Ridpath J., Hazlett M., Alves D., Dubovi E., et al. Severe acute bovine viral diarrhea in Ontario, 1993-1995. J Vet Diagn Invest 10 (1998) 27-35
13. Ellis J.A., West K.H., Cortese V.S., Myers S.L., Carman S., Martin K.M., et al. Lesions and distribution of viral antigen following an experimental infection of young seronegative calves with virulent bovine virus diarrhea virus-type II. Can J Vet Res 62 (1998) 161-169
14. Australian Centre for International Agricultural Research (ACIAR). Bovine babesiosis and anaplasmosis in the Philippines: developing a research and diagnostic capability 2004. Available from: http://www.aciar.gov.au/project/AS2/2000/098.
15. Marchette N.J., and Stiller D. The Anaplasmataceae, Bartonellaceae, and Rochalimaea quintana. In: Marchette N.J. (Ed). Ecological relationships and evolution in the Rickettsiae (1982), CRC Press, Boca Raton, Florida, USA 98-106
16. Ristic M. Anaplasmosis. In: Weinman D., and Ristic M. (Eds). Infectious blood diseases of man and animals vol. 11 (1968), Academic Press, New York, USA 473-542
17. TFRC (Tick Fever Research Center). Tick fever and disease diagnosis. Queensland, Australia: Department of Primary Industries; 1996.
18. Bock R., Jackson L., de Vos A., and Jorgensen W. Babesiosis of cattle. Parasitology 129 (2004) 247-269
19. King M.C., and Wilson A.C. Evolution at two levels in humans and chimpanzees. Science 188 (1975) 107-116
20. Michalak P., Malone J.H., Lee I.T., Hoshino D., and Ma D. Gene expression polymorphism in Drosophila populations. Mol Ecol 16 (2007) 1179-1189
21. Shnyreva M., Weaver W.M., Blanchette M., Taylor S.L., Tompa M., Fitzpatrick D.R., et al. Evolutionarily conserved sequence elements that positively regulate IFN-gamma expression in T cells. Proc Natl Acad Sci USA 101 (2004) 12622-12627
22. Gu X., and Su Z. Web-based resources for comparative genomics. Hum Genomics 2 (2005) 187-190
23. Ptacek T., and Sell S.M. A tiered approach to comparative genomics. Brief Funct Genomic Proteomic 4 (2005) 178-185
24. Caron J., Malo D., Schutta C., Templeton J.W., and Adams L.G. Genetic susceptibility of infectious diseases linked to NRAMP1 gene in farm animals. In: Cellier M., and Gros P. (Eds). The Nramp family (2004), Eurekah.com and Kluwer Academic/Plenum Publishers 16
25. Hardy K.J., and Young H.A. IFN-γ, gene structure and regulation. In: Baron S., Coppenhaver D.H., Dianzani F., Fleischmann W.R., Hughes T.K., Klimpel G.R., Niesel D.W., Stanton G.J., and Tyring S.K. (Eds). Interferon: principles and medical applications (1992), The University of Texas Medical Branch, Galveston, TX 1-15
26. Lewis D.B., and Wilson C.B. Gamma-interferon: an immunoregulatory lymphokine with immunotherapeutic potential. Pediatr Infect Dis J 9 (1990) 642-651
27. Kojima H., Aizawa Y., Yanai Y., Nagaoka K., Takeuchi M., Ohta T., et al. An essential role for NF-kappa B in IL-18-induced IFN-gamma expression in KG-1 cells. J Immunol 162 (1999) 5063-5069
28. Ye J., Cippitelli M., Dorman L., Ortaldo J.R., and Young H.A. The nuclear factor YY1 suppresses the human gamma interferon promoter through two mechanisms: inhibition of AP1 binding and activation of a silencer element. Mol Cell Biol 16 (1996) 4744-4753
29. Abbas A.K., Murphy K.M., and Sher A. Functional diversity of helper T lymphocytes. Nature 383 (1996) 787-793
30. Bradley L.M., Dalton D.K., and Croft M. A direct role for IFN-gamma in regulation of Th1 cell development. J Immunol 157 (1996) 1350-1358
31. Romagnani S. Understanding the role of Th1/Th2 cells in infection. Trends Microbiol 4 (1996) 470-473
32. Konnai S., Usui T., Ikeda M., Kohara J., Hirata T., Okada K., et al. Tumor necrosis factor-alpha genetic polymorphism may contribute to progression of bovine leukemia virus-infection. Microbes Infect 8 (2006) 2163-2171
33. An P., Thio C.L., Kirk G.D., Donfield S., Goedert J.J., and Winkler C.A. Regulatory polymorphisms in the interleukin-18 promoter are associated with hepatitis C virus clearance. J Infect Dis 198 (2008) 1159-1165
34. Cunningham L.M., Chapman C., Dunstan R., Bell M.C., and Joske D.J. Polymorphisms in the interleukin 10 gene promoter are associated with susceptibility to aggressive non-Hodgkin's lymphoma. Leuk Lymphoma 44 (2003) 251-255
35. Dhiman N., Ovsyannikova I.G., Vierkant R.A., Pankratz V.S., Jacobson R.M., and Poland G.A. Associations between cytokine/cytokine receptor single nucleotide polymorphisms and humoral immunity to measles, mumps and rubella in a Somali population. Tissue Antigens 72 (2008) 211-220
36. Nicaud V., Raoux S., Poirier O., Cambien F., O'Reilly D.S., and Tiret L. The TNF alpha/G-308A polymorphism influences insulin sensitivity in offspring of patients with coronary heart disease: the european atherosclerosis research study II. Atherosclerosis 161 (2002) 317-325
37. Usui T., Konnai S., Ohashi K., and Onuma M. Interferon-γ expression associated with suppression of bovine leukemia virus at the early phase of infection in sheep. Vet Immunol Immunopathol 115 (2007) 17-23
38. Konnai S., Usui T., Ohashi K., and Onuma M. The rapid quantitative analysis of bovine cytokine genes by real-time RT-PCR. Vet Microbiol 94 (2003) 283-294
39. World Organization for Animal Health (OIE). World animal health information system 2008. Available from: http://www.oie.int/wahis/public.php.
40. Waldvogel A.S., Hediger-Weithaler B.M., Eicher R., Zakher A., Zarlenga D.S., Gasbarre L.C., et al. Interferon-gamma and interleukin-4 mRNA expression by peripheral blood mononuclear cells from pregnant and non-pregnant cattle seropositive for bovine viral diarrhea virus. Vet Immunol Immunopathol 77 (2000) 201-212
41. Bielefeldt-Ohmann H. The pathologies of bovine viral diarrhea virus infection. A window on the pathogenesis. Vet Clin North Am Food Anim Pract 11 (1995) 447-476
42. Yamane D, Kato K, Tohya Y, Akashi H. The relationship between the viral RNA level and upregulation of innate immunity in spleen of cattle persistently infected with bovine viral diarrhea virus. Vet Microbiol 2007. doi:10.1016/j.vetmic.2007.11.004.
43. Trainin Z., Brenner J., Meirom R., and Ungar-Waron H. Detrimental effect of bovine leukemia virus (BLV) on the immunological state of cattle. Vet Immunol Immunopathol 54 (1996) 293-302
44. Klintevall K., Fuxler L., and Fossum C. Bovine leukemia virus: early reflections in blood after an experimental infection of calves. Comp Immunol Microbiol Infect Dis 20 (1997) 119-130
45. Meirom R., Moss S., Brenner J., Heller D., and Trainin Z. Levels and role of cytokines in bovine leukemia virus (BLV) infection. Leukemia 11 (1997) 219-220
46. Kabeya H., Ohashi K., and Onuma M. Host immune responses in the course of bovine leukemia virus infection. J Vet Med Sci 63 (2001) 703-708
47. Amills M., Ramiya V., Norimine J., Olmstead C.A., and Lewin H.A. Reduced IL-2 and IL-4 mRNA expression in CD4+ T cells from bovine leukemia virus-infected cows with persistent lymphocytosis. Virology 304 (2002) 1-9
48. Yakobson B., Brenner J., Ungar-Waron H., and Trainin Z. Short-termed expression of interleukin-12 during experimental BLV infection may direct disease progression to persistent lymphocytosis. Vet Immunol Immunopathol 64 (1998) 207-218
49. Gale K.R., Gartside M.G., Dimmock C.M., Zakrzewski H., and Leatch G. Peripheral blood lymphocyte proliferative responses in cattle infected with or vaccinated against Anaplasma marginale. Parasitol Res 82 (1996) 551-562
50. Mosmann T.R., Cherwinski H., Bond M.W., Giedlin M.A., and Coffman R.L. Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immunol 136 (1986) 2348-2357
51. Pedra J.H., Tao J., Sutterwala F.S., Sukumaran B., Berliner N., Bockenstedt L.K., et al. IL-12/23p40-dependent clearance of Anaplasma phagocytophilum in the murine model of human anaplasmosis. FEMS Immunol Med Microbiol 50 (2007) 401-410
52. Brown W.C., Zhu D., Shkap V., McGuire T.C., Blouin E.F., Kocan K.M., et al. The repertoire of Anaplasma marginale antigens recognized by CD4(+) T-lymphocyte clones from protectively immunized cattle is diverse and includes major surface protein 2 (MSP-2) and MSP-3. Infect Immun 66 (1998) 5414-5422
53. Kim H.Y., and Rikihisa Y. Expression of interleukin-1beta, tumor necrosis factor alpha, and interleukin-6 in human peripheral blood leukocytes exposed to human granulocytic ehrlichiosis agent or recombinant major surface protein P44. Infect Immun 68 (2000) 3394-3402
54. Grosse W.M., Kappes S.M., Laegreid W.W., Keele J.W., Chitko-McKown C.G., and Heaton M.P. Single nucleotide polymorphism (SNP) discovery and linkage mapping of bovine cytokine genes. Mamm Genome 10 (1999) 1062-1069
55. Mingala C.N., Odbileg R., Konnai S., Ohashi K., and Onuma M. Comparative assessment of Th1 and Th2 cytokines of swamp type buffalo and other bubaline breeds by molecular cloning, sequencing and phylogenetics. Vet Immunol Immunopathol 113 (2006) 348-356
56. Skoog T., van't Hooft F.M., Kallin B., Jovinge S., Boquist S., Nilsson J., et al. A common functional polymorphism (C → A substitution at position -863) in the promoter region of the tumour necrosis factor-alpha (TNF-alpha) gene associated with reduced circulating levels of TNF-alpha. Hum Mol Genet 8 (1999) 1443-1449
57. Wilson A.G., Symons J.A., McDowell T.L., McDevitt H.O., and Duff G.W. Effects of a polymorphism in the human tumor necrosis factor alpha promoter on transcriptional activation. Proc Natl Acad Sci USA 94 (1997) 3195-3199
58. Penix L., Weaver W.M., Pang Y., Young H.A., and Wilson C.B. Two essential regulatory elements in the human interferon gamma promoter confer activation specific expression in T cells. J Exp Med 178 (1993) 1483-1496
59. Sica A., Dorman L., Viggiano V., Cippitelli M., Ghosh P., Rice N., et al. Interaction of NF-kappaB and NFAT with the interferon-gamma promoter. J Biol Chem 272 (1997) 30412-30420
60. Sweetser M.T., Hoey T., Sun Y.L., Weaver W.M., Price G.A., and Wilson C.B. The roles of nuclear factor of activated T cells and ying-yang 1 in activation-induced expression of the interferon-gamma promoter in T cells. J Biol Chem 273 (1998) 34775-34783
61. Deshpande A., Nolan J.P., White P.S., Valdez Y.E., Hunt W.C., Peyton C.L., et al. TNF-alpha promoter polymorphisms and susceptibility to human papillomavirus 16-associated cervical cancer. J Infect Dis 191 (2005) 969-976
62. Singh K.K., and Schmidtke J. Single nucleotide polymorphism within the promoter region of the rhesus monkey tumor necrosis factor-alpha gene. Immunogenetics 57 (2005) 289-292
63. Radwan G.S., Brock K.V., Hogan J.S., and Smith K.L. Development of a PCR amplification assay as a screening test using bulk milk samples for identifying dairy herds infected with bovine viral diarrhea virus. Vet Microbiol 44 (1995) 77-91
64. Tajima S., Ikawa Y., and Aida Y. Complete bovine leukemia virus (BLV) provirus is conserved in BLV-infected cattle throughout the course of B-cell lymphosarcoma development. J Virol 72 (1998) 7569-7576
65. Molad T., Mazuz M.L., Fleiderovitz L., Fish L., Savitsky I., Krigel Y., et al. Molecular and serological detection of A. centrale- and A. marginale-infected cattle grazing within an endemic area. Vet Microbiol 113 (2006) 55-56
66. Figueroa J.V., Chieves L.P., Johnson G.S., and Buening G.M. Detection of Babesia bigemina-infected carriers by polymerase chain reaction amplification. J Clin Microbiol 30 (1992) 2576-2582
67. Konnai S., Usui T., Ikeda M., Kohara J., Hirata T., Okada K., et al. Imbalance of tumor necrosis factor receptors during progression in bovine leukemia virus infection. Virology 339 (2005) 239-248