Association of leishmaniasis with TNF alpha promoter and SLC11A1 gene polymorphisms in patients of two endemic areas in Mexico

• Published in: Microbes and infection 2015-05, Vol.17 (5), p.387-394
• Main Authors: Ortiz-Flores, Aaxin, De la Rosa-López, Gabriela, Zavaleta-Villa, Beatriz, Chávez-López, Susana, Pastor-Santiago, Jorge, Guzmán-Bracho, Carmen, Romero-Valdovinos, Mirza, Martínez-Hernández, Fernando, Olivo-Díaz, Angélica
• Format: Article
• Language: English
• Subjects: Case-Control Studies; Cation Transport Proteins - genetics; Cation Transport Proteins - immunology; DNA typing; Genetic Predisposition to Disease - epidemiology; Genetic susceptibility; Humans; Leishmaniasis; Leishmaniasis, Cutaneous - epidemiology; Leishmaniasis, Cutaneous - genetics; Leishmaniasis, Visceral - epidemiology; Leishmaniasis, Visceral - genetics; Mexico - epidemiology; Polymorphism, Genetic - genetics; Polymorphism, Genetic - immunology; Polymorphism, Single Nucleotide - genetics; Polymorphism, Single Nucleotide - immunology; Polymorphisms; SLC11A1; TNF-α; Tumor Necrosis Factor-alpha - genetics; Tumor Necrosis Factor-alpha - immunology
• ISSN: 1286-4579; 1769-714X
• DOI: 10.1016/j.micinf.2015.01.001

Some Single Nucleotide Polymorphisms (SNPs) of interleukins and other modulatory molecules of the immune response play an important role in susceptibility to infectious diseases, particularly those involving intracellular parasites. In this study, we evaluated allele, genotype and haplotype associations of two SNPs of the TNF-α promoter and seven of the SLC11A1 gene in 79 patients with localized cutaneous leishmaniasis (CL) and 15 with visceral leishmaniasis (VL), compared with 127 and 89 locality paired controls, respectively, from two endemic areas of Chiapas State, Mexico. None of the TNF-α alleles and genotypes was associated either to CL or to VL. Alleles rs2276631-C (P = 0.02; OR [95%CI] = 2.11 [1.16–3.86]) and rs2279015-G (P = 0.005; OR [95%CI] = 2.42 [1.33–4.41]) of SLC11A1, were associated with susceptibility to VL, whereas genotypes rs2276631 C/C (P = 0.003; OR [95%CI] = 2.65 [1.41–5.00]) and rs2279015 G/G (P = 0.018; OR [95%CI] = 2.05 [1.15–3.64]) were significantly increased in CL and VL patients, respectively. Complete haplotypes involved in susceptibility were CGCCGDins with VL and CGCCADins with CL. CGCCA was the minimal susceptibility haplotype for CL and CCG for VL. Our data suggest that SLC11A1 gene polymorphisms might have a relevant role in the pathology of leishmaniasis, directing towards susceptibility outcome of this disease in residents of an endemic area.