HIV-1 Infection Transcriptomics: Meta-Analysis of CD4+ T Cells Gene Expression Profiles.
Antonio Victor Campos CoelhoRossella GrattonJoão Paulo Britto de MeloJosé Leandro Andrade-SantosRafael Lima GuimarãesSergio CrovellaPaola Maura TricaricoLucas André Cavalcanti BrandãoPublished in: Viruses (2021)
HIV-1 infection elicits a complex dynamic of the expression various host genes. High throughput sequencing added an expressive amount of information regarding HIV-1 infections and pathogenesis. RNA sequencing (RNA-Seq) is currently the tool of choice to investigate gene expression in a several range of experimental setting. This study aims at performing a meta-analysis of RNA-Seq expression profiles in samples of HIV-1 infected CD4+ T cells compared to uninfected cells to assess consistently differentially expressed genes in the context of HIV-1 infection. We selected two studies (22 samples: 15 experimentally infected and 7 mock-infected). We found 208 differentially expressed genes in infected cells when compared to uninfected/mock-infected cells. This result had moderate overlap when compared to previous studies of HIV-1 infection transcriptomics, but we identified 64 genes already known to interact with HIV-1 according to the HIV-1 Human Interaction Database. A gene ontology (GO) analysis revealed enrichment of several pathways involved in immune response, cell adhesion, cell migration, inflammation, apoptosis, Wnt, Notch and ERK/MAPK signaling.
Keyphrases
- antiretroviral therapy
- hiv infected
- single cell
- rna seq
- human immunodeficiency virus
- cell cycle arrest
- hiv positive
- induced apoptosis
- gene expression
- hiv aids
- genome wide
- oxidative stress
- pi k akt
- immune response
- systematic review
- genome wide identification
- endoplasmic reticulum stress
- signaling pathway
- dna methylation
- cell migration
- cell proliferation
- endothelial cells
- cell adhesion
- randomized controlled trial
- hepatitis c virus
- bioinformatics analysis
- healthcare
- poor prognosis
- transcription factor
- genome wide analysis
- social media
- health information
- case control
- emergency department
- binding protein
- toll like receptor
- long non coding rna
- dendritic cells
- decision making