Department of Pathology, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, 1235 Cidade Universitária, Recife 50670-901, Brazil.
Department of Advanced Translational Microbiology, Institute for Maternal and Child Health IRCCS Burlo Garofolo, Via dell'Istria 65/1, 34137 Trieste, Italy.
Viruses. 2021 Feb 4;13(2):244. doi: 10.3390/v13020244.
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.
HIV-1 感染会引发宿主各种基因表达的复杂动态变化。高通量测序为 HIV-1 感染和发病机制增加了大量信息。RNA 测序(RNA-Seq)目前是研究多种实验条件下基因表达的首选工具。本研究旨在对 HIV-1 感染的 CD4+T 细胞样本与未感染细胞的 RNA-Seq 表达谱进行荟萃分析,以评估 HIV-1 感染背景下一致差异表达的基因。我们选择了两项研究(22 个样本:15 个实验感染和 7 个模拟感染)。与未感染/模拟感染细胞相比,我们在感染细胞中发现了 208 个差异表达基因。与之前 HIV-1 感染转录组学的研究相比,这一结果有一定的重叠,但我们根据 HIV-1 人类相互作用数据库鉴定了 64 个已知与 HIV-1 相互作用的基因。GO 分析显示,与免疫反应、细胞黏附、细胞迁移、炎症、细胞凋亡、Wnt、Notch 和 ERK/MAPK 信号通路相关的多个途径富集。