The expression of circulating hsa-miR-126-3p in dengue-infected Thai pediatric patients

Methee Sriprapun1, Jittraporn Rattanamahaphoom2,3, Pimolpachr Sriburin2,3

  • 1Department of Microbiology, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.

Insights

Circulating hsa-miR-126-3p levels are lower in pediatric dengue patients compared to controls. While not predicting severity, it shows potential as an early and late biomarker for dengue virus infection.

Area of Science:

  • Molecular biology
  • Virology
  • Pediatrics

Background:

  • Circulating microRNAs (miRNAs) are implicated in infectious disease pathogenesis.
  • Hsa-miRNA-126 (CmiR-126) is involved in dengue virus infection.
  • Pediatric dengue patients require further investigation regarding CmiR-126.

Purpose of the Study:

  • To describe CmiR-126-3p levels in pediatric dengue patients during febrile and convalescent phases.
  • To investigate correlations between CmiR-126-3p and clinical laboratory factors.
  • To assess CmiR-126-3p as a potential biomarker for dengue virus infection.

Main Methods:

  • Serum samples from dengue fever (DF), dengue hemorrhagic fever (DHF), and acute febrile illness (AFI) pediatric patients were analyzed.
  • CmiR-126-3p expression was quantified using reverse transcription quantitative real-time polymerase-chain reaction (RT-qPCR).
  • Data normalization was performed using CmiR-16-5p, and relative expression was calculated via the 2^-ΔCt method.

Main Results:

  • CmiR-126-3p expression was significantly lower in dengue patients (DF and DHF) compared to AFI controls during both febrile and convalescent phases (p < 0.05).
  • No significant differences in CmiR-126-3p levels were observed between DF and DHF, or between primary and secondary dengue infections (p > 0.05).
  • CmiR-126-3p levels increased significantly from the febrile to convalescent phase in DF patients (p = 0.025), but showed no correlation with hematocrit, WBC, platelets, or viral load.

Conclusions:

  • Hsa-miR-126-3p is involved in the pathogenesis of dengue infection.
  • Hsa-miR-126-3p may serve as a promising early and late biomarker for dengue virus infection (DENV).
  • Hsa-miR-126-3p alone cannot predict dengue severity.

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