Differences in the transcriptional responses induced by Theileria annulata infection in bovine monocytes derived from resistant and susceptible cattle breeds

International Journal for Parasitology

Volumn 38, Issue 3-4, 2008, Pages 313-325

  Jensen, Kirsty ^a   Paxton, Edith ^a   Waddington, David ^a   Talbot, Richard ^a   Darghouth, Mohamed A ^b   Glass, Elizabeth J ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b Ecole Nationale de Medecine Veterinaire   (Tunisia)

Author keywords

Bovine; Disease resistance; Host pathogen interactions; Microarray; Monocyte; Theileria annulata

Indexed keywords

PRION PROTEIN; TOLL LIKE RECEPTOR 10;

BLOOD; CATTLE; DISEASE CONTROL; DNA; EUKARYOTE; GENE EXPRESSION; GENETIC VARIATION; HOST-PATHOGEN INTERACTION; IMMUNE RESPONSE; MOLECULAR ANALYSIS; POLYMERASE CHAIN REACTION; PROTEIN; PROTOZOAN;

ARTICLE; CATTLE; CATTLE DISEASE; DISEASE COURSE; FEMALE; GENE EXPRESSION; GENE IDENTIFICATION; GENETIC CODE; GENETIC TRANSCRIPTION; IN VITRO STUDY; MALE; MICROARRAY ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; THEILERIA ANNULATA; THEILERIOSIS; UNINDEXED SEQUENCE;

ANIMALS; BREEDING; CATTLE; CATTLE DISEASES; CELLS, CULTURED; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION TO DISEASE; HOST-PARASITE INTERACTIONS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PROTOZOAN VACCINES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SPECIES SPECIFICITY; THEILERIA ANNULATA; THEILERIASIS; TRANSCRIPTION, GENETIC;

BOS; BOS INDICUS; BOS TAURUS; BOVINAE; FRIESIA; IXODIDA; PROTOZOA; THEILERIA ANNULATA;

EID: 38949106949     PISSN: 00207519     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpara.2007.08.007     Document Type: Article

References (45)

1. de Almeida C.J.G., Chiarini L.B., da Silva J.P., de Silva P.M.R., Martins M.A., and Linden R. The cellular prion protein modulates phagocytosis and inflammatory response. J. Leukocyte Biol. 77 (2005) 238-246
2. Bakheit M.A., and Latif A.A. The innate resistance of Kenana cattle to tropical theileriosis (Theileria annulata infection) in the Sudan. Ann. N.Y. Acad. Sci. 969 (2002) 159-163
3. van Beek E.M., Cochrane F., Barclay A.N., and van den Berg T.K. Signal regulatory proteins in the immune system. J. Immunol. 175 (2005) 7781-7787
4. Benjamini Y., and Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. R. Stat. Soc. B. 57 (1995) 289-300
5. Bielefeldt Ohmann H., Campos M., Snider M., Raipin N., Beshkorwayne T., Popowych Y., Lawman M.J.P., Rossi A., and Babiuik L.A. Effect of chronic administration of recombinant bovine tumour necrosis factor to cattle. Vet. Pathol. 26 (1989) 462-472
6. Brooke G.P., Parsons K.R., and Howard C.J. Cloning of two members of the SIRP alpha family of protein tyrosine phosphatase binding proteins in cattle that are expressed on monocytes and a subpopulation of dendritic cells and which mediate binding to CD4 T cells. Eur. J. Immunol. 28 (1998) 1-11
7. Brown C.G.D. Theileriidae. In: Taylor A.E.R., and Baker J.R. (Eds). In Vitro Methods of Parasite Cultivation (1987), Academic Press, New York 230-253
8. Brown D.J., Campbell J.D.M., Russell G.C., Hopkins J., and Glass E.J. T cell activation by Theileria annulata-infected macrophages correlates with cytokine production. Clin. Exp. Immunol. 102 (1995) 507-514
9. Campbell J.D.M., Howie S.E.M., Odling K.A., and Glass E.J. Theileria annulata induces aberrant T cell activation in vitro and in vivo. Clin. Exp. Immunol. 99 (1995) 203-210
10. Campbell J.D.M., Brown D.J., Nichani A.K., Howie S.E.M., Spooner R.L., and Glass E.J. A non-protective T helper 1 response against the intra-macrophage protozoan Theileria annulata. Clin. Exp. Immunol. 108 (1997) 463-470
11. Chan C.W., Kay L.S., Khadaroo R.G., Chan M.W.C., Lakatoo S., Young K.J., Zhang L., Gorczynski R.M., Cattral M., Rotstein O., and Levy G.A. Soluble fibrinogen-like protein 2/fibroleukin exhibits immunosuppressive properties: suppressing T cell proliferation and inhibiting maturation of bone marrow-derived dendritic cells. J. Immunol. 170 (2003) 4036-4044
12. Coussens P.M., Colvin C.J., Wiersma K., Abouzied A., and Sipkovsky S. Gene expression profiling of peripheral blood mononuclear cells from cattle infected with Mycobacterium paratuberculosis. Infect. Immun. 70 (2002) 5494-5502
13. Dobbelaere D., and Heussler V. Transformation of leukocytes by Theileria parva and T. annulata. Annu. Rev. Microbiol. 53 (1999) 1-42
14. Dürig J., Giese A., Schulz-Schaeffer W., Rosenthal C., Schmücker U., Bieschke J., Dührsen U., and Kretzschmar H.A. Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytes. Br. J. Haematol. 108 (2000) 488-496
15. Forsyth L.M.G., Minns F.C., Kirvar E., Adamson R.E., Hall F.R., McOrist S., Brown C.G.D., and Preston P.M. Tissue damage in cattle infected with Theileria annulata accompanied by metastasis of cytokine-producing, schizont-infected mononuclear phagocytes. J. Comp. Pathol. 120 (1999) 39-57
16. Glass E.J., and Jensen K. Resistance and susceptibility to a protozoan parasite of cattle - gene expression differences in macrophages from different breeds of cattle. Vet. Immunol. Immunopathol. 120 (2007) 20-30
17. Glass E.J., Innes E.A., Spooner R.L., and Brown C.G.D. Infection of bovine monocyte/macrophage populations with Theileria annulata and Theileria parva. Vet. Immunol. Immunopathol. 22 (1989) 355-368
18. Glass E.J., Oliver R.A., and Russell G.C. Duplicated DQ haplotypes increase the complexity of restriction element usage in cattle. J. Immunol. 165 (2000) 134-138
19. Glass E.J., Craigmile S.C., Springbett A., Preston P.M., Kirvar E., Wilkie G.M., Eckersall P.D., Hall F.R., and Brown C.G.D. The protozoan parasite, Theileria annulata, induces a distinct acute phase protein response in cattle that is associated with pathology. Int. J. Parasitol. 33 (2003) 1409-1418
20. Glass E.J., Preston P.M., Springbett A., Craigmile S., Kirvar E., Wilkie G., and Brown C.G.D. Bos taurus and Bos indicus (Sahiwal) calves respond differently to infection with Theileria annulata and produce markedly different levels of acute phase proteins. Int. J. Parasitol. 35 (2005) 337-347
21. Graham S.P., Brown D.J., Vatansever Z., Waddington D., Taylor L.H., Nichani A.K., Campbell J.D.M., Adamson R.E., Glass E.J., and Spooner R.L. Proinflammatory cytokine expression by Theileria annulata infected cell lines correlates with the pathology they cause in vivo. Vaccine 19 (2001) 2932-2944
22. Hasan U., Chaffois C., Gaillard C., Saulnier V., Merck E., Tancredi S., Guiet C., Briere F., Vlach J., Lebecque S., Trinchieri G., and Bates E.E.M. Human TLR10 is a functional receptor, expressed by B cells and plasmacytoid dendritic cells, which activates gene transcription through MyD88. J. Immunol. 174 (2005) 2942-2950
23. Heussler V.T. Theileria survival strategies and host cell transformation. In: Dobbelaere D., and McKeever D. (Eds). World Class Parasites: Volume 3: Theileria (2002), Kluwer Academic Press, Norwell 69-84
24. Jensen K., Speed D., Paxton E., Williams J.L., and Glass E.J. Construction of a normalized Bos taurus and Bos indicus macrophage specific cDNA library. Anim. Genet. 37 (2006) 75-77
25. Jensen K., Talbot R., Paxton E., Waddington D., and Glass E.J. Development and validation of a bovine macrophage specific cDNA microarray. BMC Genomics 7 (2006) 224
26. Jensen K., de Miranda Santos I.K.F., and Glass E.J. Using genomic approaches to unravel livestock (host)-tick-pathogen interactions. Trends Parasitol. 23 (2007) 439-444
27. Jongen-Lavrencic M., Peeters H.R.M., Rozemuller H., Rombouts W.J.C., Martens A.C.M., Vreugdenhil G., Pillay M., Cox P.H., Bijser M., Brutel G., Breedveld F.C., and Swaak A.J.G. IL-6-induced anaemia in rats: possible pathogenic implications for anaemia observed in chronic inflammations. Clin. Exp. Immunol. 103 (1996) 328-334
28. McGuire K., and Glass E.J. The expanding role of microarrays in the investigation of macrophage responses to pathogens. Vet. Immunol. Immunopathol. 105 (2005) 259-275
29. Minjauw B., and de Castro J.J. Host resistance to ticks and tick-borne diseases: its role in integrated control. In: Axford R.F.E., Bishop S.C., Nicholas F.W., and Owen J.B. (Eds). Breeding for Disease Resistance in Farm Animals. 2nd ed. (2000), CABI, Wallingford 153-169
30. Minjauw, B., McLeod, A., 2003. Tick borne diseases and poverty. The impact of ticks and tick-borne diseases on the livelihoods of small-scale and marginal livestock owners in India and eastern and southern Africa. Research report, DFID Animal Health Programme. ().
31. O'Neill L.A.J. TLRs: Professor Mechnikov, sit on your hat. Trends Immunol. 25 (2004) 687-693
32. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 29 (2001) e45
33. Preston P.M., Brown C.G.D., Bell-Sakyi L., Richardson W., and Sanderson A. Tropical theileriosis in Bos taurus and Bos taurus cross Bos indicus calves: response to infection with graded does of sporozoites of Theileria annulata. Res. Vet. Sci. 53 (1992) 230-243
34. Preston P.M., Darghouth M., Boulter N.R., Hall F.R., Tall R., Kirvar E., and Brown C.G.D. A dual role for immunosuppressor mechanisms in infection with Theileria annulata: well-regulated suppressor macrophages help in recovery from infection; profound immunosuppression promotes non-healing disease. Parasitol. Res. 88 (2002) 522-534
35. Robinson P.M. Theileria annulata and its transmission - a review. Trop. Anim. Health Prod. 14 (1982) 3-12
36. Rozen S., and Skaletsky H.J. Primer3 on the WWW for general users and for biologist programmers. In: Krawetz S., and Misener S. (Eds). Bioinformatics Methods and Protocols: Methods in Molecular Biology (2000), Humana Press, Totowa
37. Sager H., Davis W.C., Dobbelaere D.A., and Jungi T.W. Macrophage-parasite relationship in theileriosis. Reversible phenotypic and functional dedifferentiation of macrophages infected with Theileria annulata. J. Leukocyte Biol. 61 (1997) 459-468
38. Schultz J., Milpetz F., Bork P., and Ponting C.P. SMART, a simple modular architecture research tool: identification of signalling domains. Proc. Natl. Acad. Sci. USA 95 (1998) 5857-5864
39. Smyth G.K. Linear models and empirical Bayes methods for assessing differential expression in microarray experiments. Stat. Appl. Genet. Mol. Biol. 3 (2004) 3
40. Smyth G.K. Limma: linear models for microarray data. In: Gentleman R., Carey V., Dudoit S., Irizarry R., and Huber W. (Eds). Bioinformatics and Computational Biology Solutions using R and Bioconductor (2005), Springer, New York
41. Spooner R.L., Innes E.A., Glass E.J., and Brown C.G.D. Theileria annulata and T. parva infect and transform different bovine mononuclear cells. Immunology 66 (1989) 284-288
42. Weiss D.J., Evanson O.A., Deng M., and Abrahamsen M.S. Gene expression and antimicrobial activity of bovine macrophages in response to Mycobacterium avium subsp. paratuberculosis. Vet. Pathol. 41 (2004) 326-337
43. Weiss D.J., Evanson O.A., Deng M.Q., and Abrahamsen M.S. Sequential patterns of gene expression by bovine monocyte-derived macrophages associated with ingestion of mycobacterial organisms. Microb. Pathogen. 37 (2004) 215-224
44. Werling D., Ruryk A., Heaney J., Moeller E., and Brownlie J. Ability to differentiate between cp and ncp BVDV by microarrays: towards an application in clinical veterinary medicine?. Vet. Immunol. Immunopathol. 108 (2005) 157-164
45. Wedlock D.N., Kawakami R.P., Koach J., Buddle B.M., and Collins D.M. Differences of gene expression in bovine alveolar macrophages infected with virulent and attenuated isogenic strains of Mycobacterium bovis. Int. Immunopharmacol. 6 (2006) 957-961