Linking Chronic Infection and Autoimmune Diseases: Mycobacterium avium Subspecies paratuberculosis, SLC11A1 Polymorphisms and Type-1 Diabetes Mellitus

被引:50
作者
Paccagnini, Daniela
Sieswerda, Lee
Rosu, Valentina
Masala, Speranza
Pacifico, Adolfo
Gazouli, Maria
Ikonomopoulos, John
Ahmed, Niyaz
Zanetti, Stefania
Sechi, Leonardo A.
机构
[1] Dipartimento di Scienze Biomediche, Sezione di Microbiologia Clinica e Sperimentale, Sassari
[2] Bay District Health Unit 999, Thunder Bay, ON
[3] Servizio di Diabetologia, Clinica Medica Universitaria di Sassari, Sassari
[4] Department of Biology, School of Medicine, University of Athens, Athens
[5] Department of Anatomy-Physiology, Faculty of Animal Science, Agricultural University of Athens, Athens
[6] Pathogen Biology Laboratory, Department of Biotechnology, University of Hyderabad, Hyderabad
关键词
D O I
10.1371/journal.pone.0007109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The etiology of type 1 diabetes mellitus (T1DM) is still unknown; numerous studies are performed to unravel the environmental factors involved in triggering the disease. SLC11A1 is a membrane transporter that is expressed in late endosomes of antigen presenting cells involved in the immunopathogenic events leading to T1DM. Mycobacterium avium subsp. paratuberculosis (MAP) has been reported to be a possible trigger in the development of T1DM. Methodology/Principal Findings: Fifty nine T1DM patients and 79 healthy controls were genotyped for 9 polymorphisms of SLC11A1 gene, and screened for the presence of MAP by PCR. Differences in genotype frequency were evaluated for both T1DM patients and controls. We found a polymorphism in the SLC11A1 gene (274C/T) associated to type 1 diabetic patients and not to controls. The presence of MAP DNA was also significantly associated with T1DM patients and not with controls. Conclusions/Significance: The 274C/T SCL11A1 polymorphism was found to be associated with T1DM as well as the presence of MAP DNA in blood. Since MAP persists within macrophages and it is also processed by dendritic cells, further studies are necessary to evaluate if mutant forms of SLC11A1 alter the processing or presentation of MAP antigens triggering thereby an autoimmune response in T1DM patients.
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