Association of polymorphisms and abnormal methylation of several autophagy genes with pulmonary tuberculosis susceptibility, clinical manifestations in a Chinese population.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Hua Niu, Dong-Ping Wang, Xue-Qian Cai, Hao-Hui Fang, Ye Li
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引用次数: 0

Abstract

Background: Studies have shown that autophagy was closely involved in host defense against mycobacteria, and genetic variations in autophagy genes were related to susceptibility to multiple diseases. We conducted this observational study to analyze the role of autophagy related genes polymorphisms and promoter methylation in the pathogenesis of pulmonary tuberculosis (PTB).

Methods: Ten single nucleotide polymorphisms (SNPs) in four autophagy related genes (ATG16L1, ATG5, IRGM, ULK1) were genotyped in 496 PTB patients and 498 controls using SNPscan technique, and the methylation levels of these genes were detected by MethylTarget technique in 98 PTB patients and 97 controls.

Results: We found that ATG16L1 gene rs2241880 GG genotype frequency was significantly increased in PTB patients than that in controls. While, no significant association was found between PTB risk and ATG16L1 rs6754677, ATG5 rs2245214, rs510432, IRGM rs1000113, rs10065172, rs12658239, ULK1 rs7138581, rs9481, rs12297124. Haplotype analysis showed that ATG16L1 GA haplotype was associated with the increased risk to PTB, and ATG5 CC haplotype was related to the decreased risk to PTB. Stratification analysis demonstrated that ATG16L1 rs6754677, IRGM rs1000113, rs10065172 polymorphism were associated with pulmonary infection, and ULK1 rs7138581 polymorphism was related to fever, drug-induced liver injury in PTB patients. Compared with controls, ATG16L1 methylation level was significantly decreased in PTB, while ATG5, IRGM methylation levels were not significantly changed. Rs1000113, rs10065172, rs12658239 variants in IRGM had a major impact on IRGM methylation level in PTB patients.

Conclusion: ATG16L1, ATG5 genes variation and ATG16L1 gene methylation level were associated with the genetic background of PTB, while IRGM, ULK1 genes variations showed no significant association with PTB.

中国人群中几个自噬基因多态性和异常甲基化与肺结核易感性和临床表现的关系
背景:研究表明,自噬与宿主对分枝杆菌的防御密切相关,自噬基因的遗传变异与多种疾病的易感性有关。我们进行了这项观察性研究,以分析自噬相关基因多态性和启动子甲基化在肺结核(PTB)发病机制中的作用。方法:采用SNPscan技术对496例PTB患者和498例对照者的4个自噬相关基因(ATG16L1、ATG5、IRGM、ULK1)的10个单核苷酸多态性(snp)进行基因分型,并采用MethylTarget技术检测98例PTB患者和97例对照者中这些基因的甲基化水平。结果:我们发现ATG16L1基因rs2241880 GG基因型频率在肺结核患者中明显高于对照组。而ATG16L1 rs6754677、ATG5 rs2245214、rs510432、IRGM rs1000113、rs10065172、rs12658239、ULK1 rs7138581、rs9481、rs12297124与PTB风险无显著相关性。单倍型分析显示,ATG16L1 GA单倍型与PTB发病风险增加相关,ATG5 CC单倍型与PTB发病风险降低相关。分层分析发现ATG16L1 rs6754677、IRGM rs1000113、rs10065172多态性与肺部感染相关,ULK1 rs7138581多态性与PTB患者发热、药物性肝损伤相关。与对照组相比,PTB患者的ATG16L1甲基化水平显著降低,而ATG5、IRGM甲基化水平无显著变化。IRGM中的Rs1000113、rs10065172、rs12658239变异对PTB患者IRGM甲基化水平有重要影响。结论:ATG16L1、ATG5基因变异及ATG16L1基因甲基化水平与PTB遗传背景相关,而IRGM、ULK1基因变异与PTB无显著相关性。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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