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对 WSSV 感染的红螯螯虾(Cherax quadricarinatus)造血组织干细胞的差异基因表达谱分析。

Differential gene expression profile from haematopoietic tissue stem cells of red claw crayfish, Cherax quadricarinatus, in response to WSSV infection.

机构信息

State Key Laboratory of Marine Environmental Science, College of Oceanography and Environmental Science, Xiamen University, Xiamen 361005, Fujian, PR China.

出版信息

Dev Comp Immunol. 2011 Jul;35(7):716-24. doi: 10.1016/j.dci.2011.02.015. Epub 2011 Mar 17.

Abstract

White spot syndrome virus (WSSV) is one of the most important viral pathogens in crustaceans. During WSSV infection, multiple cell signaling cascades are activated, leading to the generation of antiviral molecules and initiation of programmed cell death of the virus infected cells. To gain novel insight into cell signaling mechanisms employed in WSSV infection, we have used suppression subtractive hybridization (SSH) to elucidate the cellular response to WSSV challenge at the gene level in red claw crayfish haematopoietic tissue (Hpt) stem cell cultures. Red claw crayfish Hpt cells were infected with WSSV for 1h (L1 library) and 12h (L12 library), respectively, after which the cell RNA was prepared for SSH using uninfected cells as drivers. By screening the L1 and L12 forward libraries, we have isolated the differentially expressed genes of crayfish Hpt cells upon WSSV infection. Among these genes, the level of many key molecules showed clearly up-regulated expression, including the genes involved in immune responses, cytoskeletal system, signal transduction molecules, stress, metabolism and homestasis related genes, and unknown genes in both L1 and L12 libraries. Importantly, of the 2123 clones screened, 176 novel genes were found the first time to be up-regulated in WSSV infection in crustaceans. To further confirm the up-regulation of differentially expressed genes, the semi-quantitative RT-PCR were performed to test twenty randomly selected genes, in which eight of the selected genes exhibited clear up-regulation upon WSSV infection in red claw crayfish Hpt cells, including DNA helicase B-like, multiprotein bridging factor 1, apoptosis-linked gene 2 and an unknown gene-L1635 from L1 library; coatomer gamma subunit, gabarap protein gene, tripartite motif-containing 32 and an unknown gene-L12-254 from L2 library, respectively. Taken together, as well as in immune and stress responses are regulated during WSSV infection of crayfish Hpt cells, our results also light the significance of cytoskeletal system, signal transduction and other unknown genes in the regulation of antiviral signals during WSSV infection.

摘要

白斑综合征病毒(WSSV)是甲壳类动物最重要的病毒病原体之一。在 WSSV 感染过程中,多个细胞信号级联被激活,导致抗病毒分子的产生和受感染细胞的程序性细胞死亡的启动。为了深入了解 WSSV 感染中细胞信号转导机制,我们使用抑制性消减杂交(SSH)在红螯螯虾造血组织(Hpt)干细胞培养物中从基因水平阐明了细胞对 WSSV 挑战的反应。红螯螯虾 Hpt 细胞分别用 WSSV 感染 1 小时(L1 文库)和 12 小时(L12 文库),然后用未感染的细胞作为驱动物从感染细胞中提取 RNA 进行 SSH。通过筛选 L1 和 L12 正向文库,我们分离出了 WSSV 感染后红螯螯虾 Hpt 细胞差异表达的基因。在这些基因中,许多关键分子的水平显示出明显的上调表达,包括参与免疫反应、细胞骨架系统、信号转导分子、应激、代谢和稳态相关基因以及 L1 和 L12 文库中的未知基因。重要的是,在筛选的 2123 个克隆中,有 176 个新基因首次在甲壳类动物的 WSSV 感染中被发现上调。为了进一步证实差异表达基因的上调,我们进行了半定量 RT-PCR 测试,测试了 20 个随机选择的基因,其中 8 个基因在红螯螯虾 Hpt 细胞的 WSSV 感染中明显上调,包括 L1 文库中的 DNA 解旋酶 B 样、多蛋白桥接因子 1、凋亡相关基因 2 和未知基因-L1635;L2 文库中的衣壳蛋白γ亚基、gabapap 蛋白基因、三部分基序蛋白 32 和未知基因-L12-254。总之,在红螯螯虾 Hpt 细胞的 WSSV 感染过程中,免疫和应激反应受到调节,我们的结果还表明细胞骨架系统、信号转导和其他未知基因在 WSSV 感染过程中抗病毒信号的调节中的重要性。

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