Additive host genetic factors influence fecal egg excretion rates during Schistosoma mansoni infection in a rural area in Brazil

被引:38
作者
Bethony, J
Williams, JT
Blangero, J
Kloos, H
Gazzinelli, A
Soares, B
Coelho, L
Alves-Fraga, L
Williams-Blangero, S
Loverde, PT
Correa-Oliveira, R
机构
[1] SW Fdn Biomed Res, Dept Genet, San Antonio, TX USA
[2] Univ Calif San Francisco, Med Ctr, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[3] Univ Fed Minas Gerais, Escola Enfermagem, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Inst Geosci, Ctr Sensoriamento Remoto, BR-30270971 Belo Horizonte, MG, Brazil
[5] Univ Vale Rio Doce, CENBIOS, Lab Immunol & Pesquisa, Governado Valadares, MG, Brazil
[6] SUNY Buffalo, Sch Med & Biomed Sci, Dept Microbiol, Buffalo, NY 14216 USA
[7] Fiocruz MS, Ctr Pesquisas Rene Rachou, Immunol Lab, BR-30190 Belo Horizonte, MG, Brazil
[8] George Washington Univ, Dept Microbiol & Trop Med, Washington, DC USA
关键词
D O I
10.4269/ajtmh.2002.67.336
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
This study quantifies the influence of shared household and kinship on egg counts during Schistosoma mansoni infection in a sample from rural Brazil. Detailed genealogic information allowed assignment of 597 individuals to 6 multihousehold pedigrees residing in 145 households. A variance component method was used to partition egg counts into shared household, additive genetic, and individual-specific environmental effects. Host additive genetic effects consistently accounted for a large proportion of the variation in egg counts: 43% in an unadjusted model and 40% in model adjusted for covariates. In a model that examined the confounding of shared household with kinship, additive genetic effects still accounted for 27% of the variation in egg counts and shared household only 12%. The consistently important role for host additive genetic factors on the variation in egg counts points to new ways of modeling and understanding the mechanisms that contribute to trait variation during infection with S. mansoni.
引用
收藏
页码:336 / 343
页数:8
相关论文
共 58 条
[41]   Further evidence suggesting the presence of a locus, on human chromosome 5q31-q33, influencing the intensity of infection with Schistosoma mansoni [J].
MullerMyhsok, B ;
Stelma, FF ;
GuisseSow, F ;
Muntau, B ;
Thye, T ;
Burchard, GD ;
Gryseels, B ;
Horstmann, RD .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :452-454
[42]  
POLDERMAN AM, 1979, TROP GEOGR MED, V31, P465
[43]  
POLDERMAN AM, 1985, ANN SOC BELG MED TR, V65, P251
[44]   MALUMFASHI ENDEMIC DISEASES RESEARCH-PROJECT .3. URINARY SCHISTOSOMIASIS - LONGITUDINAL-STUDY [J].
PUGH, RNH ;
GILLES, HM .
ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1978, 72 (05) :471-482
[45]  
Rodrigues V, 1996, AM J HUM GENET, V59, P453
[46]  
SCOTT D, 1982, B WORLD HEALTH ORGAN, V60, P89
[47]  
Searle SR., 1992, VARIANCE COMPONENTS, DOI DOI 10.1002/9780470316856
[48]  
Searle SR., 1971, LINEAR MODELS
[49]   ASYMPTOTIC PROPERTIES OF MAXIMUM-LIKELIHOOD ESTIMATORS AND LIKELIHOOD RATIO TESTS UNDER NONSTANDARD CONDITIONS [J].
SELF, SG ;
LIANG, KY .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1987, 82 (398) :605-610
[50]   EDF STATISTICS FOR GOODNESS OF FIT AND SOME COMPARISONS [J].
STEPHENS, MA .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1974, 69 (347) :730-737