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Differential Expression of Human MicroRNAs During Dengue Virus Infection in THP-1 Monocytes
- Source :
- Frontiers in Cellular and Infection Microbiology, Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
- Publication Year :
- 2021
- Publisher :
- Frontiers Media S.A., 2021.
-
Abstract
- Dengue virus (DENV) is the most widespread arbovirus, responsible for a wide range of clinical manifestations, varying from self-limited illness to severe hemorrhagic fever. Dengue severity is associated with host intense proinflammatory response and monocytes have been considered one of the key cell types involved in the early steps of DENV infection and immunopathogenesis. To better understand cellular mechanisms involved in monocyte infection by DENV, we analyzed the expression levels of 754 human microRNAs in DENV-infected THP-1 cells, a human monocytic cell line. Eleven human microRNAs showed differential expression after DENV infection and gene ontology and enrichment analysis revealed biological processes potentially affected by these molecules. Five downregulated microRNAs were significantly linked to cellular response to stress, four to cell death/apoptosis, two to innate immune responses and one upregulated to vesicle mediated, TGF-β signaling, phosphatidylinositol mediated signaling, lipid metabolism process and blood coagulation.
- Subjects :
- Microbiology (medical)
Programmed cell death
THP-1 Cells
viruses
Immunology
Biology
Dengue virus
medicine.disease_cause
Arbovirus
Microbiology
Monocytes
Dengue fever
Proinflammatory cytokine
virus-host
Cellular and Infection Microbiology
medicine
Humans
THP1 cell line
Innate immune system
microRNA
Monocyte
virus diseases
Dengue Virus
biochemical phenomena, metabolism, and nutrition
Brief Research Report
medicine.disease
dengue
Immunity, Innate
QR1-502
MicroRNAs
Infectious Diseases
medicine.anatomical_structure
monocyte
gene expression
Subjects
Details
- Language :
- English
- ISSN :
- 22352988
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Frontiers in Cellular and Infection Microbiology
- Accession number :
- edsair.doi.dedup.....ead3911e9939d4e175381f3871166a03