Grupo Genética Molecular (GENMOL), Universidad de Antioquia, Carrera 53 No. 61-30, Lab 430. Medellín, Colombia.
Grupo Malaria-Facultad de Medicina, Universidad de Antioquia, Carrera 53 No. 61-30, Lab 610, Medellín, Colombia.
Infect Genet Evol. 2021 Jan;87:104675. doi: 10.1016/j.meegid.2020.104675. Epub 2020 Dec 13.
Host genetics is an influencing factor in the manifestation of infectious diseases. In this study, the association of mild malaria with 28 variants in 16 genes previously reported in other populations and/or close to ancestry-informative markers (AIMs) selected was evaluated in an admixed 736 Colombian population sample. Additionally, the effect of genetic ancestry on phenotype expression was explored. For this purpose, the ancestral genetic composition of Turbo and El Bagre was determined. A higher Native American ancestry trend was found in the population with lower malaria susceptibility [odds ratio (OR) = 0.416, 95% confidence interval (95% CI) = 0.234-0.740, P = 0.003]. Three AIMs presented significant associations with the disease phenotype (MID1752, MID921, and MID1586). The first two were associated with greater malaria susceptibility (D/D, OR = 2.23, 95% CI = 1.06-4.69, P = 0.032 and I/D-I/I, OR = 2.14, 95% CI = 1.18-3.87, P = 0.011, respectively), and the latter has a protective effect on the appearance of malaria (I/I, OR = 0.18, 95% CI = 0.08-0.40, P < 0.0001). After adjustment by age, sex, municipality, and genetic ancestry, genotype association analysis showed evidence of association with malaria susceptibility for variants in or near IL1B, TLR9, TREM1, IL10RA, and CD3G genes: rs1143629-IL1B (G/A-A/A, OR = 0.41, 95% CI = 0.21-0.78, P = 0.0051), rs352139-TLR9 (T/T, OR = 0.28, 95% CI = 0.11-0.72, P = 0.0053), rs352140-TLR9 (C/C, OR = 0.41, 95% CI = 0.20-0.87, P = 0.019), rs2234237-TREM1 (T/A-A/A, OR = 0.43, 95% CI = 0.23-0.79, P = 0.0056), rs4252246-IL10RA (C/A-A/A, OR = 2.11, 95% CI = 1.18-3.75, P = 0.01), and rs1561966-CD3G (A/A, OR = 0.20, 95% CI = 0.06-0.69, P = 0.0058). The results showed the participation of genes involved in immunological processes and suggested an effect of ancestral genetic composition over the traits analyzed. Compared to the paisa population (Antioquia), Turbo and El Bagre showed a strong decrease in European ancestry and an increase in African and Native American ancestries. Also, a novel association of two single nucleotide polymorphisms with malaria susceptibility was identified in this study.
宿主遗传学是传染病表现的一个影响因素。在这项研究中,评估了先前在其他人群中报道的与轻度疟疾相关的 16 个基因中的 28 个变体与选择的接近祖先信息标记(AIMs)之间的关联,并在混合的 736 名哥伦比亚人群样本中进行了探索。此外,还研究了遗传祖先对表型表达的影响。为此,确定了 Turbo 和 El Bagre 的祖先遗传组成。在疟疾易感性较低的人群中发现了更高的美洲原住民遗传趋势[优势比(OR)=0.416,95%置信区间(95%CI)=0.234-0.740,P=0.003]。三个 AIM 与疾病表型呈显著关联(MID1752、MID921 和 MID1586)。前两个与更高的疟疾易感性相关(D/D,OR=2.23,95%CI=1.06-4.69,P=0.032 和 I/D-I/I,OR=2.14,95%CI=1.18-3.87,P=0.011),而后者对疟疾的出现具有保护作用(I/I,OR=0.18,95%CI=0.08-0.40,P<0.0001)。在按年龄、性别、市和遗传祖先进行调整后,基因型关联分析显示,与 IL1B、TLR9、TREM1、IL10RA 和 CD3G 基因中的变体或附近的疟疾易感性相关联的证据:rs1143629-IL1B(G/A-A/A,OR=0.41,95%CI=0.21-0.78,P=0.0051)、rs352139-TLR9(T/T,OR=0.28,95%CI=0.11-0.72,P=0.0053)、rs352140-TLR9(C/C,OR=0.41,95%CI=0.20-0.87,P=0.019)、rs2234237-TREM1(T/A-A/A,OR=0.43,95%CI=0.23-0.79,P=0.0056)、rs4252246-IL10RA(C/A-A/A,OR=2.11,95%CI=1.18-3.75,P=0.01)和 rs1561966-CD3G(A/A,OR=0.20,95%CI=0.06-0.69,P=0.0058)。结果表明,参与免疫过程的基因参与其中,并表明祖先遗传组成对分析的特征有影响。与 paisa 人群(安蒂奥基亚)相比,Turbo 和 El Bagre 显示出欧洲血统的强烈减少和非洲和美洲原住民血统的增加。此外,本研究还确定了两个与疟疾易感性相关的新单核苷酸多态性的关联。