Gene-expression profiling discriminates between cerebral malaria (CM) - Susceptible mice and CM-resistant mice

被引:45
作者
Delahaye, NF
Coltel, N
Puthier, D
Flori, L
Houlgatte, R
Iraqi, FA
Nguyen, C
Grau, GE
Rihet, P
机构
[1] Univ Mediterranee, IFR 48, Fac Pharm, Lab Pharmacogenet Malad Parasitaires EA864, F-13385 Marseille 5, France
[2] Univ Mediterranee, IFR 48, CNRS, UMR 6020,Immunopathol Grp, F-13385 Marseille 5, France
[3] INSERM, ERM 206, TAGC, Marseille, France
[4] Int Livestock Res Inst, Nairobi, Kenya
关键词
D O I
10.1086/498579
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The development of cerebral malaria ( CM) in mice with Plasmodium berghei ANKA infection is under genetic control. Brain gene-expression patterns were investigated in well-defined genetically CM-resistant (CM-R; BALB/c and DBA/2) and CM-susceptible (CM-S; C57BL/6 and CBA/J) mice by use of cDNA microarrays. By combining transcriptional profiling with rigorous statistical methods and cluster analysis, we identified a set of 69 genes that perfectly discriminated between mouse strains and between CM-R and CM-S mice. The analysis of gene ontological terms revealed that the genes that clustered and were related to susceptibility to CM preferentially belonged to some biological process classes, such as those pertaining to immune responses. Using a false discovery rate of 5% and the Welch t test, we identified 31 genes with consistent differential expression between CM-R and CM-S mice. These data indicate that microarray analysis may be useful for identification of candidate genes that are potentially responsible for resistance or susceptibility to mouse CM and suggest that candidate genes identified in mice could be specifically tested in humans for an association with disease severity.
引用
收藏
页码:312 / 321
页数:10
相关论文
共 69 条
[51]  
2-K
[52]   Fas and perforin contribute to the pathogenesis of murine cerebral malaria [J].
Potter, S ;
Chaudhri, G ;
Hansen, A ;
Hunt, NH .
REDOX REPORT, 1999, 4 (06) :333-335
[53]   A general survey of thymocyte differentiation by transcriptional analysis of knockout mouse models [J].
Puthier, D ;
Joly, F ;
Irla, M ;
Saade, M ;
Victorero, G ;
Loriod, B ;
Nguyen, C .
JOURNAL OF IMMUNOLOGY, 2004, 173 (10) :6109-6118
[54]   Malaria in humans:: Plasmodium falciparum blood infection levels are linked to chromosome 5q31-q33 [J].
Rihet, P ;
Traoré, Y ;
Abel, L ;
Aucan, C ;
Traoré-Leroux, T ;
Fumoux, F .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :498-505
[55]  
Scragg IG, 1999, EUR J IMMUNOL, V29, P2636, DOI 10.1002/(SICI)1521-4141(199908)29:08&lt
[56]  
2636::AID-IMMU2636&gt
[57]  
3.0.CO
[58]  
2-Y
[59]   Transcriptional profiling reveals suppressed erythropoiesis, up-regulated glycolysis, and interferon-associated responses in murine malaria [J].
Sexton, AC ;
Good, RT ;
Hansen, DS ;
D'Ombrain, MC ;
Buckingham, L ;
Simpson, K ;
Schofield, L .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (07) :1245-1256
[60]   The glucocorticoid attenuated response genes GARG-16, GARG-39, and GARG-49/IRG2 encode inducible proteins containing multiple tetratricopeptide repeat domains [J].
Smith, JB ;
Herschman, HR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 330 (02) :290-300