Journal Article

Genetic Variation in Autophagy-Related Genes Influences the Risk and Phenotype of Buruli Ulcer

Capela, Carlos, Silva-Gomes, Rita, Pedrosa, Jorge, Makoutode, Michel, Menino, João Filipe, Sopoh, Ghislain Emmanuel, Cunha, Cristina, Dossou, Ange Dodji, Fraga, Alexandra Gabriel, Rodrigues, Fernando, Carvalho, Agostinho

2016

Overview

Buruli ulcer (BU) is a severe necrotizing human skin disease caused by Mycobacterium ulcerans. Clinically, presentation is a sum of these diverse pathogenic hits subjected to critical immune-regulatory mechanisms. Among them, autophagy has been demonstrated as a cellular process of critical importance. Since microtubules and dynein are affected by mycolactone, the critical pathogenic exotoxin produced by M. ulcerans, cytoskeleton-related changes might potentially impair the autophagic process and impact the risk and progression of infection. Genetic variants in the autophagy-related genes NOD2, PARK2 and ATG16L1 has been associated with susceptibility to mycobacterial diseases. Here, we investigated their association with BU risk, its severe phenotypes and its progression to an ulcerative form. Genetic variants were genotyped using KASPar chemistry in 208 BU patients (70.2% with an ulcerative form and 28% in severe WHO category 3 phenotype) and 300 healthy endemic controls. The rs1333955 SNP in PARK2 was significantly associated with increased susceptibility to BU [odds ratio (OR), 1.43; P = 0.05]. In addition, both the rs9302752 and rs2066842 SNPs in NOD2 gee significantly increased the predisposition of patients to develop category 3 (OR, 2.23; P = 0.02; and OR 12.7; P = 0.03, respectively, whereas the rs2241880 SNP in ATG16L1 was found to significantly protect patients from presenting the ulcer phenotype (OR, 0.35; P = 0.02). Our findings indicate that specific genetic variants in autophagy-related genes influence susceptibility to the development of BU and its progression to severe phenotypes.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Adolescent / Adult / Analysis / Autophagy / Autophagy (Cytology) / Autophagy-Related Proteins / Biology and Life Sciences / Buruli ulcer / Buruli Ulcer - epidemiology / Buruli Ulcer - genetics / Buruli Ulcer - pathology / Carrier Proteins - genetics / Child / Cytoskeleton / Development and progression / Disease / Female / Funding / Gender / Genes / Genetic diversity / Genetic Predisposition to Disease / Genetic variance / Genetic variation / Genomics / Genotyping Techniques / Haplotypes / Health care / Host-Pathogen Interactions / Humans / Infections / Influence / Male / Medicine and Health Sciences / Mycobacterium ulcerans - immunology / Nod2 Signaling Adaptor Protein - genetics / Pathogens / Polymorphism, Single Nucleotide / Risk Assessment / Risk factors / Skin diseases / Tropical diseases / Ubiquitin-Protein Ligases - genetics / Ulcers / Young Adult