Complex genetic control of susceptibility to malaria in mice

被引:66
作者
Fortin, A
Stevenson, MM
Gros, P
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Ctr Study Host Resistance, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Ctr Canc, Montreal, PQ H3G 1Y6, Canada
关键词
malaria; complex trait; mouse model; recombinant congenic; host defense; genetic susceptibility;
D O I
10.1038/sj.gene.6363841
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Malaria is a major infectious disease worldwide, with over 1 million deaths in African children every year. The molecular pathways of pathogenesis of the Plasmodium parasite and the host mechanisms of defense against this infection remain poorly understood. Epidemiological studies, together with linkage analyses in endemic areas have clearly pointed at a genetic component of innate susceptibility and severity of disease. In humans, this genetic trait is complex, and has been studied in a mouse experimental model over the past few years. Inbred strains of mice show different degrees of susceptibility to infection with Plasmodium chabaudi, and the genetic component of these inter-strain differences has been studied in standard informative backcross and F2 populations, as well as in recombinant inbred strains and more recently, in recombinant congenic strains. These studies have shown that genetic susceptibility to malaria is also complex in mice, and have led to the mapping of major susceptibility Char (Chabaudi resistance) loci, located on chromosomes 9 (Char1), 8 (Char2), 17 (Char3) and 3 (Char4).
引用
收藏
页码:177 / 186
页数:10
相关论文
共 81 条
[1]  
ABEL L, 1992, AM J HUM GENET, V50, P1308
[2]   ROLE OF MACROPHAGE-DERIVED NITRIC-OXIDE IN SUPPRESSION OF LYMPHOCYTE-PROLIFERATION DURING BLOOD-STAGE MALARIA [J].
AHVAZI, BC ;
JACOBS, P ;
STEVENSON, MM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 58 (01) :23-31
[3]   α+-thalassemia protects children against disease caused by other infections as well as malaria [J].
Allen, SJ ;
O'Donnell, A ;
Alexander, NDE ;
Alpers, MP ;
Peto, TEA ;
Clegg, JB ;
Weatherall, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14736-14741
[4]   Familial correlation of immunoglobulin g subclass responses to Plasmodium falciparum antigens in Burkina Faso [J].
Aucan, C ;
Traoré, Y ;
Fumoux, F ;
Rihet, P .
INFECTION AND IMMUNITY, 2001, 69 (02) :996-1001
[5]   TESTOSTERONE-INDUCED ABROGATION OF SELF-HEALING OF PLASMODIUM-CHABAUDI MALARIA IN B10 MICE - MEDIATION BY SPLEEN-CELLS [J].
BENTEN, WPM ;
BETTENHAEUSER, U ;
WUNDERLICH, F ;
VANVLIET, E ;
MOSSMANN, H .
INFECTION AND IMMUNITY, 1991, 59 (12) :4486-4490
[6]   Vital involvement of a natural killer cell activation receptor in resistance to viral infection [J].
Brown, MG ;
Dokun, AO ;
Heusel, JW ;
Smith, HRC ;
Beckman, DL ;
Blattenberger, EA ;
Dubbelde, CE ;
Stone, LR ;
Scalzo, AA ;
Yokoyama, WM .
SCIENCE, 2001, 292 (5518) :934-937
[7]   Temporal expression of an H2-linked locus in host response to mouse malaria [J].
Burt, RA ;
Baldwin, TM ;
Marshall, VM ;
Foote, SJ .
IMMUNOGENETICS, 1999, 50 (5-6) :278-285
[8]   New French government aims to boost research job prospects [J].
Butler, D .
NATURE, 1997, 387 (6633) :535-535
[9]  
CHIPPAUX JP, 1992, REV EPIDEMIOL SANTE, V40, P240
[10]   PLASMODIUM-CHABAUDI - A RODENT MALARIA MODEL FOR INVIVO AND INVITRO CYTOADHERENCE OF MALARIA PARASITES IN THE ABSENCE OF KNOBS [J].
COX, J ;
SEMOFF, S ;
HOMMEL, M .
PARASITE IMMUNOLOGY, 1987, 9 (05) :543-561