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Journal of Infectious Diseases and Therapy ISSN: 2332-0877 | Volume: 6
Infectious Diseases
4
th
Annual Congress on
Neglected Tropical & Infectious Diseases
5
th
International Conference on
August 29-30, 2018 | Boston, USA
&
Differential expressionofmiRNAinperipheral blood cells fromacute dengue anddengue hemorrhagic
fever patients
Harsha Hapugaswatte, Kapila N Seneviratne, H Suharshi S Perera, Ranjan Premaratne
and
Nimanthi Jayathilaka
University of Kelaniya, Sri Lanka
D
engue is the most prevalent arboviral disease transmitted by mosquitoes common in tropical areas of the world. Lack of
proper medication or vaccines for dengue fever and inability to distinguish severe cases of dengue fever (DF) known as
dengue hemorrhagic fever (DHF) during the early stages of infection, renders this disease life-threatening for people living
in endemic areas. Early symptoms of DHF are similar to those of non-life threatening DF. However, DHF patients manifest
plasma leakage, elevated hematocrit, and pleural effusions after 3-5days of fever. Early diagnosis and disease management
can alleviate DHF related complications. Therefore, biomarkers that distinguish DHF at the acute phase of infection can help
reduce mortality. Due to their role in post-transcriptional regulation of cellular gene expression and remarkable stability, altered
expression of miRNA can serve as clinically relevant biomarkers. Therefore, we evaluated the expression of five miRNA targets
in Peripheral blood cells (PBC) collected from 20 DF and 20 DHF positive patients within four days of fever onset by qRT-PCR.
Relative expression of has-let-7e, has-miR-30b, has-miR-30e-3p, has-mir-33a, and has-miR-150-5p were evaluated against the
geometric mean of has-miR-103a-3p and has-miR-16-5p as reference genes. While has- let7e, has-miR-30b, has-miR-30e-3p
and hsa-mir-33° did not show differential expression between and DHF patients during the acute phase of infection, has-miR-
150-5p showed over two-fold upregulation indicating that miR-150 may serve as an early biomarker of DHF.
Biography
Nimanthi Jayathilaka earned her PhD from University of Southern California and conducted her postdoctoral studies at University of California, San Diego. Currently
she serves as a Senior Lecturer in Chemistry at the University of Kelaniya, Sri Lanka. Her primary research interest is transcriptional regulation in diseases.
njayathi@kln.ac.lkNimanthi Jayathilaka et al., J Infect Dis Ther 2018, Volume 6
DOI: 10.4172/2332-0877-C3-045




