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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.lk

Nimanthi Jayathilaka et al., J Infect Dis Ther 2018, Volume 6

DOI: 10.4172/2332-0877-C3-045