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首页> 外文期刊>Parasites Vectors >Screening for differentially expressed miRNAs in Aedes albopictus (Diptera: Culicidae) exposed to DENV-2 and their effect on replication of DENV-2 in C6/36 cells
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Screening for differentially expressed miRNAs in Aedes albopictus (Diptera: Culicidae) exposed to DENV-2 and their effect on replication of DENV-2 in C6/36 cells

机译:在暴露于DENV-2的白纹伊蚊(Diptera:Culicidae)中筛选差异表达的miRNA及其对C6 / 36细胞中DENV-2复制的影响

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Abstract BackgroundThe mosquito Aedes albopictus is an important vector for dengue virus (DENV) transmission. The midgut is the first barrier to mosquito infection by DENV, and this barrier is a critical factor affecting the vector competence of the mosquito. However, the molecular mechanism of the interaction between midgut and virus is unknown.ResultsSix small libraries of Ae. albopictus midgut RNAs were constructed, three of which from mosquitoes that were infected with DENV-2 after feeding on infected blood, and another three that remained uninfected with DENV-2 after feeding on same batch of infected blood. A total of 46 differentially expressed miRNAs were identified of which 17 significant differentially expressed miRNAs were selected. Compared to microRNA expression profiles of mosquitoes that were uninfected with DENV-2, 15 microRNAs were upregulated and two were downregulated in mosquitoes that were infected with DENV-2. Among these differentially expressed microRNAs, miR-1767, miR-276-3p, miR-4448 and miR-622 were verified by stem-loop qRT-PCR in samples from seven-day-infected and uninfected midguts and chosen for an in vitro transient transfection assay. miR-1767 and miR-276-3p enhanced dengue virus replication in C6/36 cells, and miR-4448 reduced dengue virus replication.ConclusionsTo our knowledge, this study is the first to reveal differences in expression levels between mosquitoes infected and uninfected with DENV-2 after feeding on an infected blood meal. It provides useful information on microRNAs expressed in the midgut of Aedes albopictus after exposure to the virus.
机译:摘要背景蚊白纹伊蚊是登革热病毒(DENV)传播的重要载体。中肠是DENV感染蚊子的第一个障碍,而该障碍是影响蚊子媒介能力的关键因素。然而,中肠病毒与病毒相互作用的分子机制尚不清楚。构造了白皮虫中肠RNA,其中三个来自蚊子,它们在喂食被感染的血液后被DENV-2感染,另外三个在喂食了同一批被感染的血液后仍未被DENV-2感染。总共鉴定出46种差异表达的miRNA,其中选择了17种显着差异表达的miRNA。与未感染DENV-2的蚊子的microRNA表达谱相比,在感染DENV-2的蚊子中,microRNA的表达上调了15个,而其中两个则下调了。在这些差异表达的microRNA中,miR-1767,miR-276-3p,miR-4448和miR-622已通过茎环qRT-PCR在7天感染和未感染的中肠样品中进行了验证,并选择用于体外瞬时转染测定。 miR-1767和miR-276-3p增强了登革热病毒在C6 / 36细胞中的复制,而miR-4448减少了登革热病毒的复制。喂食被感染的血粉后-2。它提供了有关暴露于病毒后在白纹伊蚊中肠表达的microRNA的有用信息。

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