Dunstan Sarah J, Nguyen Thi Hue, Rockett Kirk, Forton Julian, Morris Andrew P, Diakite Mahamadou, Mai Ngoc Lanh, Le Thi Phuong, House Deborah, Parry Christopher M, Ha Vinh, Nguyen T Hieu, Dougan Gordon, Tran Tinh Hien, Kwiatowski Dominic, Farrar Jeremy J
Oxford University Clinical Research Unit, Hospital for Tropical Diseases, 190 Ben Ham Tu, Quan 5, District 5, Ho Chi Minh City, Vietnam.
Hum Genet. 2007 Aug;122(1):51-61. doi: 10.1007/s00439-007-0372-9. Epub 2007 May 15.
The genomic region surrounding the TNF locus on human chromosome 6 has previously been associated with typhoid fever in Vietnam (Dunstan et al. in J Infect Dis 183:261-268, 2001). We used a haplotypic approach to understand this association further. Eighty single nucleotide polymorphisms (SNPs) spanning a 150 kb region were genotyped in 95 Vietnamese individuals (typhoid case/mother/father trios). A subset of data from 33 SNPs with a minor allele frequency of >4.3% was used to construct haplotypes. Fifteen SNPs, which tagged the 42 constructed haplotypes were selected. The haplotype tagging SNPs (T1-T15) were genotyped in 380 confirmed typhoid cases and 380 Vietnamese ethnically matched controls. Allelic frequencies of seven SNPs (T1, T2, T3, T5, T6, T7, T8) were significantly different between typhoid cases and controls. Logistic regression results support the hypothesis that there is just one signal associated with disease at this locus. Haplotype-based analysis of the tag SNPs provided positive evidence of association with typhoid (posterior probability 0.821). The analysis highlighted a low-risk cluster of haplotypes that each carry the minor allele of T1 or T7, but not both, and otherwise carry the combination of alleles 121221111 at T1-T11, further supporting the one associated signal hypothesis. Finally, individuals that carry the typhoid fever protective haplotype 121221111 also produce a relatively low TNF-alpha response to LPS.
人类6号染色体上肿瘤坏死因子(TNF)基因座周围的基因组区域此前已被证实与越南的伤寒热有关(Dunstan等人,《传染病杂志》,2001年,第183卷,第261 - 268页)。我们采用单倍型分析方法进一步探究这种关联。在95名越南个体(伤寒病例/母亲/父亲三联体)中,对跨越150 kb区域的80个单核苷酸多态性(SNP)进行了基因分型。使用来自33个次要等位基因频率>4.3%的SNP的部分数据构建单倍型。选择了15个SNP,这些SNP标记了构建的42种单倍型。在380例确诊的伤寒病例和380名越南种族匹配的对照中对单倍型标签SNP(T1 - T15)进行基因分型。伤寒病例组和对照组之间,7个SNP(T1、T2、T3、T5、T6、T7、T8)的等位基因频率存在显著差异。逻辑回归结果支持了该基因座仅存在一个与疾病相关信号的假设。基于单倍型的标签SNP分析提供了与伤寒相关的阳性证据(后验概率0.821)。该分析突出了一个低风险单倍型簇,每个单倍型携带T1或T7的次要等位基因,但不同时携带两者,并且在T1 - T11处携带等位基因组合121221111,进一步支持了单一相关信号的假设。最后,携带伤寒热保护性单倍型121221111的个体对脂多糖(LPS)产生的肿瘤坏死因子 - α(TNF - α)反应也相对较低。