Cytokine responses of Holstein and Sahiwal zebu derived monocytes after mycobacterial infection

Tropical Animal Health and Production

Volumn 44, Issue 3, 2012, Pages 651-655

  Vordermeier, Martin ^a   Ameni, Gobena ^b   Glass, Elizabeth J ^c  

^a VETERINARY LABORATORIES AGENCY   (United Kingdom)

^b ADDIS ABABA UNIVERSITY   (Ethiopia)

^c UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

Bovine tuberculosis; Cattle; Cytokines; Holstein; Mycobacterium bovis; Mycobacterium tuberculosis; Zebu

Indexed keywords

INTERLEUKIN DERIVATIVE; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL; ANIMAL HUSBANDRY; ARTICLE; BOVINE TUBERCULOSIS; CATTLE; CELL CULTURE; FEMALE; GENETIC PREDISPOSITION; GENETICS; IMMUNOLOGY; INNATE IMMUNITY; METABOLISM; MICROBIOLOGY; MONOCYTE; MYCOBACTERIUM BOVIS; MYCOBACTERIUM TUBERCULOSIS; SPECIES DIFFERENCE;

ANIMAL HUSBANDRY; ANIMALS; CATTLE; CELLS, CULTURED; FEMALE; GENETIC PREDISPOSITION TO DISEASE; IMMUNITY, INNATE; INTERLEUKINS; MONOCYTES; MYCOBACTERIUM BOVIS; MYCOBACTERIUM TUBERCULOSIS; SPECIES SPECIFICITY; TUBERCULOSIS, BOVINE; TUMOR NECROSIS FACTOR-ALPHA;

BOS; BOS INDICUS; BOS TAURUS; BOVINAE; MYCOBACTERIUM BOVIS; MYCOBACTERIUM TUBERCULOSIS;

EID: 84856693278     PISSN: 00494747     EISSN: 15737438     Source Type: Journal    
DOI: 10.1007/s11250-011-9950-x     Document Type: Article

References (29)

1. Aldwell, F. E., Wedlock, D. N., Buddle, B. M. 1996. Bacterial metabolism, cytokine mRNA transcription and viability of bovine alveolar macrophages infected with Mycobacterium bovis BCG or virulent M. bovis. Immunology and Cell Biology 74, 45-51.
2. Ameni, G., Aseffa, A., Engers, H., Young, D., Gordon, S., Hewinson, G., Vordermeier, M. 2007. High prevalence and increased severity of pathology of bovine tuberculosis in Holsteins compared to zebu breeds under field cattle husbandry in central Ethiopia. Clinical and Vaccine Immunolology, 14, 1356-1361.
3. Ameni, G., Hewinson, G., Aseffa, A., Young, D., Vordermeier, M. 2008. Appraisal of interpretation criteria for the comparative intradermal tuberculin test for diagnosis of tuberculosis in cattle in central Ethiopia. Clinical and Vaccine Immunolology, 15, 1272-1276.
4. Amirzargar, A. A., Naroueynejad, M., Khosravi, F., Dianat, S., Rezaei, N., Mytilineos, J., Nikbin, B. 2008. Cytokine single nucleotide polymorphisms in Iranian populations. European Cytokine Network, 19, 104-112.
5. Bakheit, M. A., Latif, A. A. 2002. The innate resistance of Kenana cattle to tropical theileriosis (Theileria annulata infection) in the Sudan. Annals of the New York Academy of Science, 969, 159-163.
6. Berg, S., Firdessa, R., Habtamu, M., Gadisa, E., Mengistu, A., Yamuah, L., Ameni, G., Vordermeier, M., Robertson, B. D., Smith, N. H., Engers, H., Young, D., Hewinson, R. G., Aseffa, A., Gordon, S. V. 2009. The burden of mycobacterial disease in Ethiopian cattle: implications for public health. PLoS ONE 4, e5068.
7. Carmichael, J. 1939. Bovine tuberculosis in the tropics, with special reference to Uganda, part 1. Journal of Comparative Pathology and Therapy, 52, 322-335.
8. Coad, M., Clifford, D., Rhodes, S. G., Hewinson, R. G., Vordermeier, H. M., Whelan, A. O. 2010. Repeat tuberculin skin testing leads to desensitisation in naturally infected tuberculous cattle which is associated with elevated interleukin-10 and decreased interleukin-1 beta responses. Veterinary Research 41, 14.
9. Correia, J. W., Freitas, M. V., Queiroz, J. A., PereiraPerrin, M., Cavadas, B. 2009. Interleukin-6 blood levels in sensitive and multiresistant tuberculosis. Infection 37, 138-141.
10. de Jong, E., Suddason, T., Lord, G. M. 2010. Translational mini-review series on Th17 cells: development of mouse and human T helper 17 cells. Clinical and Experimental Immunology, 159, 148-158.
11. Djoba Siawaya, J. F., Beyers, N., van Helden, P., Walzl, G. 2009. Differential cytokine secretion and early treatment response in patients with pulmonary tuberculosis. Clinical and Experimental Immunology, 156, 69-77.
12. Glass, E. J., Jensen, K. 2007. Resistance and susceptibility to a protozoan parasite of cattle-gene expression differences in macrophages from different breeds of cattle. Veterinary Immunology and Immunopatholology, 120, 20-30.
13. Hall, L. J., Clare, S., Dougan, G. 2010. NK cells influence both innate and adaptive immune responses after mucosal immunization with antigen and mucosal adjuvant. Journal of Immunology, 184, 4327-4337.
14. Jensen, K., Paxton, E., Waddington, D., Talbot, R., Darghouth, M. A., Glass, E. J. 2008. Differences in the transcriptional responses induced by Theileria annulata infection in bovine monocytes derived from resistant and susceptible cattle breeds. International Journal of Parasitology, 38, 313-325.
15. Khader, S. A., Bell, G. K., Pearl, J. E., Fountain, J. J., Rangel-Moreno, J., Cilley, G. E., Shen, F., Eaton, S. M., Gaffen, S. L., Swain, S. L., Locksley, R. M., Haynes, L., Randall, T. D., Cooper, A. M. 2007. IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge. Nature Immunolology, 8, 369-377.
16. Ladel, C. H., Blum, C., Dreher, A., Reifenberg, K., Kopf, M., Kaufmann, S. H. 1997. Lethal tuberculosis in interleukin-6-deficient mutant mice. Infection and Immunity, 65, 4843-4849.
17. Larcombe, L. A., Orr, P. H., Lodge, A. M., Brown, J. S., Dembinski, I. J., Milligan, L. C., Larcombe, E. A., Martin, B. D., Nickerson, P. W. 2008. Functional gene polymorphisms in Canadian aboriginal populations with high rates of tuberculosis. Journal of Infectious Disease, 198, 1175-1179.
18. Liston, W. G., Soparkar, M. B. 1917. The susceptibility of Indian Milch cows to tuberculosis. Indian Journal of Medical Research, 5, 19-71.
19. Naessens, J., Teale, A. J., Sileghem, M. 2002. Identification of mechanisms of natural resistance to African trypanosomiasis in cattle. Veterinary Immunology and Immunopathology, 87, 187-194.
20. Pokkali, S., Das, S. D. 2009. Augmented chemokine levels and chemokine receptor expression on immune cells during pulmonary tuberculosis. Human Immunology, 70, 110-115.
21. Radaeva, T. V., Kondratieva, E. V., Sosunov, V. V., Majorov, K. B., Apt, A. 2008. A human-like TB in genetically susceptible mice followed by the true dormancy in a Cornell-like model. Tuberculosis (Edinb), 88, 576-585.
22. Reed, S. G., Coler, R. N., Dalemans, W., Tan, E. V., DeLa Cruz, E. C., Basaraba, R. J., Orme, I. M., Skeiky, Y. A., Alderson, M. R., Cowgill, K. D., Prieels, J. P., Abalos, R. M., Dubois, M. C., Cohen, J., Mettens, P., Lobet, Y. 2009. Defined tuberculosis vaccine, Mtb72F/AS02A, evidence of protection in cynomolgus monkeys. Proceedings of the National Academy of Science USA, 106, 2301-2306.
23. Rhodes, S. G., Sawyer, J., Whelan, A. O., Dean, G. S., Coad, M., Ewer, K. J., Waldvogel, A. S., Zakher, A., Clifford, D. J., Hewinson, R. G., Vordermeier, H. M. 2007. Is interleukin-4delta3 splice variant expression in bovine tuberculosis a marker of protective immunity? Infection and Immunity, 75, 3006-3013.
24. Sharma, A. K., Vanaayya, P. R., Parihar, N. S. 1985. Tuberculosis in cattle: a retrospective study based on necroscopy. Indian Journal of Veterinary Pathology, 9, 17-18.
25. Soparkar, M. B. 1927. The relative susceptibility of Indian Milch cattle of various breeds to tuberculosis. Indian Journal of Medical Research, 8, 755-779.
26. Stern, J. N., Keskin, D. B., Romero, V., Zuniga, J., Encinales, L., Li, C., Awad, C., Yunis, E. J. 2009. Molecular signatures distinguishing active from latent tuberculosis in peripheral blood mononuclear cells, after in vitro antigenic stimulation with purified protein derivative of tuberculin (PPD) or Candida: a preliminary report. ImmunologyResearch, 45, 1-12.
27. Tsikas, D. 2007. Analysis of nitrite and nitrate in biological fluids by assays based on the Griess reaction: appraisal of the Griess reaction in the L-arginine/nitric oxide area of research. Journal of Chromatography B, 851, 51-70.
28. Vordermeier, H. M., Villarreal-Ramos, B., Cockle, P. J., McAulay, M., Rhodes, S. G., Thacker, T., Gilbert, S. C., McShane, H., Hill, A. V., Xing, Z., Hewinson, R. G. 2009. Viral booster vaccines improve Mycobacterium bovis BCG-induced protection against bovine tuberculosis. Infection and Immunity, 77, 3364-3373.
29. Welsh, K. J., Abbott, A. N., Hwang, S. A., Indrigo, J., Armitige, L. Y., Blackburn, M. R., Hunter, R. L., Jr., Actor, J. K. 2008. A role for tumour necrosis factor-alpha, complement C5 and interleukin-6 in the initiation and development of the mycobacterial cord factor trehalose 6, 6′-dimycolate induced granulomatous response. Microbiology, 154, 1813-1824.