The 863C>A and 1031T>C Single Nucleotide Polymorphisms (SNPs) in the Tumor Necrosis Factor Alpha (TNF-α) Promoter Gene May Not Be Putative Predictors of HBV Endemicity

Author:

Kafeero Hussein Mukasa12ORCID,Ndagire Dorothy3,Ocama Ponsiano4,Kato Charles Drago5,Kateete David Patrick6,Walusansa Abdul23,Kudamba Ali78,Edgar Kigozi6,Katabazi Fred Ashaba6,Namaganda Maria Magdalene6,Ssenku Jamilu E.38,Wampande Eddie5,Kajumbula Henry1,Sendagire Hakim1

Affiliation:

1. Department of Microbiology, College of Health Sciences, Makerere University, Kampala P.O. Box 7062, Uganda

2. Department of Medical Microbiology, Habib Medical School, Faculty of Health Sciences, Islamic University in Uganda, Kampala P.O. Box 7689, Uganda

3. Department of Plant Sciences, Microbiology and Biotechnology, College of Natural Sciences, Makerere University, Kampala P.O. Box 7062, Uganda

4. Department of medicine, College of Health Sciences, Makerere University, Kampala P.O. Box 7062, Uganda

5. Department of Biomolecular Resources & Biolab Sciences (BBS), College of Veterinary Medicine, Animal Resources and Biosecurity (COVAB), Makerere University, Kampala P.O. Box 7062, Uganda

6. Department of Molecular Biology and Immunology, College of Health Sciences, Makerere University, Kampala P.O. Box 7062, Uganda

7. Department of Physiology, Habib Medical School, Faculty of Health Sciences, Islamic University in Uganda, Kampala P.O. Box 7689, Uganda

8. Department of Biological Sciences, Faculty of Science, Islamic University in Uganda, Mbale P.O. Box 2555, Uganda

Abstract

Background: Genetic polymorphisms within the gene loci of the promoter region of tumor necrosis factor (TNF) alpha have been associated with the pathogenesis of hepatitis B virus (HBV) infection. In Uganda, there is a wide variation in the HBV endemicity, ranging from low endemicity, through moderate endemicity, to hyper-endemicity. However, the underlying reasons for this disparity in HBV burden are not fully elucidated. Thus, we aimed to test the hypothesis that the TNF-α-863C/A and -1031T/C polymorphic sites may have an effect on the difference between the burden of HBV in our country. We screened 384 participants, from which a sample of 134 was drawn, to determine the HBV, TNF-α-863C/A, and TNF-α-863T/C genotypes. The nucleotide BLAST was used to match the unknown targeted sequence obtained from the Sanger sequence against the known deposited sequence. This process unveiled the base substitution mutation and the HBV genotypes. The odds ratio (OR) and Chi-square test of proportions were used for the analysis. All the analyses were performed using SPSS version 26.0 and MedCalc software version 20.010 at 95% CI. A p < 0.05 was considered statistically significant. Results: The prevalence of both the TNF-α-863C/A and the TNF-α-1031T/C genotypes and their alleles did not differ significantly by endemicity (p > 0.05). However, the prevalence of the nucleotide substitution mutations for TNF-α-863C>A and TNF-α-1031T>C was significantly low for all the study groups (p < 0.05). Conclusion: The TNF-α gene promoter at the TNF-α-863C/A and 1031T/C positions is conserved in our population and may not affect the endemicity of HBV infection. However, future research should focus on the use of nationwide samples in order to reach concreate determinations regarding the role of the TNF-α polymorphisms in the risk/resolution of HBV infections in an African or Black population.

Funder

Makerere University Research and Innovations Fund

Publisher

MDPI AG

Subject

General Medicine

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3