Susceptibility to visceral leishmaniasis in the domestic dog is associated with MHC class II polymorphism

被引:92
作者
Quinnell, RJ [1 ]
Kennedy, LJ
Barnes, A
Courtenay, O
Dye, C
Garcez, LM
Shaw, MA
Carter, SD
Thomson, W
Ollier, WER
机构
[1] Washington & Lee Univ, Sch Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Manchester, Ctr Integrated Genom Med Res, Manchester, Lancs, England
[3] Univ Liverpool, Mammalian Immunogenet Res Grp, Liverpool L69 3BX, Merseyside, England
[4] Univ Warwick, Ecol & Epidemiol Grp, Dept Sci Biol, Coventry CV4 7AL, W Midlands, England
[5] WHO, Geneva, Switzerland
[6] Inst Evandro Chagas, Belem, Para, Brazil
基金
英国惠康基金;
关键词
DLA; MHC class II; domestic dog; visceral leishmaniasis; Leishmania infantum;
D O I
10.1007/s00251-003-0545-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Zoonotic visceral leishmaniasis (VL) is a disease of dogs, humans and other animals caused by the intracellular macrophage parasite Leishmania infantum. We examined the relationship between DLA class 11 alleles (DRB1, DQA1, DQB1) and the course of infection in a cohort of Brazilian mongrel dogs exposed to natural L. infantum infection. DLA alleles were typed by sequence-based typing. DLA-DRB1 genotype was significantly associated with levels of anti-Leishmania IgG and parasite status assessed by PCR. Dogs with DLA-DRB1 *01502 had higher levels of specific IgG and an increased risk of being parasite positive compared with dogs without this allele, controlling for other alleles and significant variables. No significant associations were seen for DLA-DQA1 or DLA-DQB1 alleles. These results suggest that the DLA-DRB1 locus plays a role in determining susceptibility to canine VL. As the domestic dog is the main reservoir for human infection, the identification of genetic factors influencing canine resistance or susceptibility to VL may provide insights into the immunology and potential control through vaccination of VL.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 34 条
[1]  
Altet L, 2002, INFECT IMMUN, V70, P2763, DOI 10.1128/IAI.70.6.2763-2771.2002
[2]   Leishmania and human immunodeficiency virus coinfection: The first 10 years [J].
Alvar, J ;
Canavate, C ;
GutierrezSolar, B ;
Jimenez, M ;
Laguna, F ;
LopezVelez, R ;
Molina, R ;
Moreno, J .
CLINICAL MICROBIOLOGY REVIEWS, 1997, 10 (02) :298-+
[3]  
BLACKWELL J, 1980, NATURE, V283, P72, DOI 10.1038/283072a0
[4]   Genetic susceptibility to leishmanial infections: Studies in mice and man [J].
Blackwell, JM .
PARASITOLOGY, 1996, 112 :S67-S74
[5]   POLYMORPHISM IN TUMOR-NECROSIS-FACTOR GENES ASSOCIATED WITH MUCOCUTANEOUS LEISHMANIASIS [J].
CABRERA, M ;
SHAW, MA ;
SHARPLES, C ;
WILLIAMS, H ;
CASTES, M ;
CONVIT, J ;
BLACKWELL, JM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) :1259-1264
[6]   MALNUTRITION AS A RISK FACTOR FOR SEVERE VISCERAL LEISHMANIASIS [J].
CERF, BJ ;
JONES, TC ;
BADARO, R ;
SAMPAIO, D ;
TEIXEIRA, R ;
JOHNSON, WD .
JOURNAL OF INFECTIOUS DISEASES, 1987, 156 (06) :1030-1033
[7]   EPIDEMIOLOGY OF CANINE LEISHMANIASIS - A COMPARATIVE SEROLOGICAL STUDY OF DOGS AND FOXES IN AMAZON BRAZIL [J].
COURTENAY, O ;
MACDONALD, DW ;
LAINSON, R ;
SHAW, JJ ;
DYE, C .
PARASITOLOGY, 1994, 109 :273-279
[8]  
COURTENAY O, 1998, THESIS U LONDON
[9]   MALNUTRITION, AGE AND THE RISK OF PARASITIC DISEASE - VISCERAL LEISHMANIASIS REVISITED [J].
DYE, C ;
WILLIAMS, BG .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1993, 254 (1339) :33-39
[10]   STUDY OF THE ASSOCIATION OF HLA CLASS-I ANTIGENS WITH KALA-AZAR [J].
FAGHIRI, Z ;
TABEI, SZ ;
TAHERI, F .
HUMAN HEREDITY, 1995, 45 (05) :258-261