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Updated: Jan 31, 2026

MicroRNA-based Regulation of Picornavirus Tropism
Published on: February 6, 2017
microRNA-27a and microRNA-146a SNP in cerebral malaria
Saw Thu Wah1,2, Hathairad Hananantachai3, Jintana Patarapotikul3
1Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Bangkok, Thailand.
Background:
During Plasmodium falciparum infection, microRNA expression alters in brain tissue of mice with cerebral malaria compared to noninfected controls. MicroRNA regulates gene expression post-transcriptionally to influence biological processes. Cerebral malaria pathology caused mainly by the immunological disorder. We hypothesize that single-nucleotide polymorphism in a microRNA influences microRNA biogenesis or target gene recognition and altering susceptibility to cerebral malaria.
Methods:
We performed a literature search based on immunological mechanism and applied microRNA-related single-nucleotide polymorphisms database to examine candidate microRNA SNPs possibly responsible for cerebral malaria. MicroRNA-27a and microRNA-146a are supposed to involve in cerebral malaria pathology. To assess the relationship of microRNA SNP to cerebral malaria outcome, we performed TaqMan Genotyping Assays in 110 cerebral malaria and 207 uncomplicated malaria cases for three candidate microRNA SNPs (rs895819 of microRNA-27a, rs57095329 and rs2910164 of microRNA-146a).
Results:
Our study detected no significant difference in genotype and allele frequency of individual microRNA SNPs as well as in haplotypes of microRNA-146a between these two groups of malaria patients in Thailand. Hardy-Weinberg disequilibrium of rs57095329 in the cerebral malaria group showed a heterozygous excess which might be due to natural selection.
Conclusion:
Our data supported that the candidate microRNA SNPs have no major role to develop cerebral malaria.
Insights
Single-nucleotide polymorphisms (SNPs) in microRNAs do not appear to significantly influence susceptibility to cerebral malaria. This study found no major role for candidate microRNA SNPs in the development of cerebral malaria in Thai patients.
Area of Science:
- Genetics
- Immunology
- Molecular Biology
Background:
- Cerebral malaria is linked to altered microRNA expression in brain tissue.
- MicroRNAs regulate gene expression post-transcriptionally, impacting biological processes.
- Cerebral malaria pathology is primarily driven by immunological disorders.
Purpose of the Study:
- To investigate the hypothesis that single-nucleotide polymorphisms (SNPs) in microRNAs affect susceptibility to cerebral malaria.
- To examine microRNA SNPs potentially involved in cerebral malaria pathogenesis.
- To assess the association between specific microRNA SNPs and cerebral malaria outcomes.
Main Methods:
- Literature search on immunological mechanisms and microRNA SNP databases.
- Genotyping assays (TaqMan) for three candidate microRNA SNPs (rs895819, rs57095329, rs2910164) in 110 cerebral malaria and 207 uncomplicated malaria cases.
- Analysis of genotype, allele frequencies, and haplotypes.
Main Results:
- No significant differences were found in genotype or allele frequencies for individual microRNA SNPs or microRNA-146a haplotypes between patient groups.
- Hardy-Weinberg disequilibrium (heterozygous excess) was observed for rs57095329 in the cerebral malaria group, suggesting potential natural selection.
- The investigated microRNA SNPs did not show a significant association with cerebral malaria development.
Conclusions:
- Candidate microRNA SNPs investigated in this study do not play a major role in the development of cerebral malaria.
- Further research may be needed to explore other genetic or immunological factors contributing to cerebral malaria susceptibility.
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