Understanding bovine trypanosomiasis and trypanotolerance: the promise of functional genomics

被引:40
作者
Hill, EW
O'Gorman, GM
Agaba, M
Gibson, JP
Hanotte, O
Kemp, SJ
Naessens, J
Coussens, PM
MacHugh, DE [1 ]
机构
[1] Univ Coll Dublin, Fac Agrifood & Environm, Anim Genom Lab, Dept Anim Sci, Dublin 4, Ireland
[2] Univ Coll Dublin, Fac Agrifood & Environm, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[3] Int Livestock Res Inst, Nairobi 00100, Kenya
[4] Univ Liverpool, Sch Biol Sci, Liverpool L69 7ZD, Merseyside, England
[5] Michigan State Univ, Dept Anim Sci, Ctr Anim Funct Genom, E Lansing, MI 48824 USA
基金
爱尔兰科学基金会;
关键词
cattle; trypanosome; parasitaemia; trypanotolerance; cDNA microarray; gene expression;
D O I
10.1016/j.vetimm.2005.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
African bovine trypanosomiasis, caused by the protozoan parasite Trypanosoma congolense, is endemic throughout sub-Saharan Africa and is a major constraint on livestock production. A promising approach to disease control is to understand and exploit naturally evolved trypanotolerance. We describe the first attempt to investigate the transcriptional response of susceptible Boran (Bos indicus) cattle to trypanosome infection via a functional genomics approach using a bovine total leukocyte (BOTL) cDNA microarray platform. Four mate Boran cattle were experimentally infected with T congolense and peripheral blood mononuclear cells (PBMC) were collected before infection and 13, 17, 23 and 30 days post-infection (dpi). A reference experimental design was employed using a universal bovine reference RNA pool. Data were normalised to the median of a set of invariant genes (GAPDH) and BRB-Array tools was used to search for statistically significant differentially expressed genes between each time-point. Using a set of 20 microarray hybridisations, we have made a significant contribution to understand the temporal transcriptional response of bovine PBMC in vivo to a controlled trypanosome infection. The greatest changes were evident 13 dpi after parasites were first detected in the blood. Significant differences were observed in clusters of protein kinase C subunits and MHC class I/II related molecules. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 258
页数:12
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