Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu 610041, P. R. China.
Division of Pulmonary Disease, West China Hospital, Sichuan University, Chengdu 610041, P. R. China.
Sci Rep. 2016 Jun 23;6:28530. doi: 10.1038/srep28530.
Tuberculosis remains a global public health problem, and its immunopathogenesis is still poorly understood. In this study, 25 single nucleotide polymorphisms (SNPs) in the WNT pathway were evaluated in relation to tuberculosis risk in a Chinese Han discovery set, and 6 candidate susceptible SNPs were further validated in a Chinese Tibetan cohort. Luciferase reporter assay, RT-qPCR and Western blot were used to assess the functionality of the important WNT polymorphisms. Five polymorphisms were associated with tuberculosis susceptibility after Bonferroni correction: SFRP1 rs4736958, CTNNB1 rs9859392, rs9870255 and rs3864004 showed decreased tuberculosis risk; SFRP1 rs7832767 was related to an increased risk (OR = 1.81, 95% CI = 1.30-2.52, p = 0.010). Patients with TT genotype of rs4736958 and rs7832767 correlated with higher CRP concentrations (p = 0.003, <0.001, respectively). Functional assays revealed that mutant alleles of rs9859392 (G), rs9870255 (C) and rs3864004 (A) were associated with significantly decreased transcriptional activity, lower CTNNB1 mRNA expression and p-β-catenin level, which were consistent with their effects of decreasing TB risk. Our results provide evidences that WNT pathway polymorphisms influence tuberculosis susceptibility and host immune response to Mycobacterium tuberculosis, suggesting that these variations may serve as novel markers for identifying the risk of developing tuberculosis.
结核病仍然是一个全球性的公共卫生问题,其免疫发病机制仍知之甚少。在这项研究中,评估了 WNT 通路中的 25 个单核苷酸多态性(SNP)与中国汉族发现人群中结核病风险的关系,并且在 6 名中国藏族队列中进一步验证了 6 个候选易感 SNP。荧光素酶报告基因检测、RT-qPCR 和 Western blot 用于评估重要的 WNT 多态性的功能。经过 Bonferroni 校正后,有 5 个多态性与结核病易感性相关:SFRP1 rs4736958、CTNNB1 rs9859392、rs9870255 和 rs3864004 显示结核病风险降低;SFRP1 rs7832767 与风险增加相关(OR=1.81,95%CI=1.30-2.52,p=0.010)。rs4736958 和 rs7832767 的 TT 基因型患者与 CRP 浓度升高相关(p=0.003,<0.001)。功能检测显示,rs9859392(G)、rs9870255(C)和 rs3864004(A)的突变等位基因与转录活性显著降低、CTNNB1 mRNA 表达和 p-β-catenin 水平降低相关,这与它们降低结核病风险的作用一致。我们的结果提供了证据,表明 WNT 通路多态性影响结核病易感性和宿主对结核分枝杆菌的免疫反应,表明这些变化可能作为识别发生结核病风险的新型标志物。