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鲑鱼气单胞菌感染大西洋鲑鱼肾脏的磷酸蛋白质组学分析。

Phosphoproteomic analyses of kidneys of Atlantic salmon infected with Aeromonas salmonicida.

机构信息

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.

Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, 266235, China.

出版信息

Sci Rep. 2019 Feb 14;9(1):2101. doi: 10.1038/s41598-019-38890-3.

Abstract

Aeromonas salmonicida (A. salmonicida) is a pathogenic bacterium that causes furunculosis and poses a significant global risk, particularly in economic activities such as Atlantic salmon (Salmo salar) farming. In a previous study, we identified proteins that are significantly upregulated in kidneys of Atlantic salmon challenged with A. salmonicida. Phosphoproteomic analyses were conducted to further clarify the dynamic changes in protein phosphorylation patterns triggered by bacterial infection. To our knowledge, this is the first study to characterize phosphorylation events in proteins from A. salmonicida-infected Atlantic salmon. Overall, we identified over 5635 phosphorylation sites in 3112 proteins, and 1502 up-regulated and 77 down-regulated proteins quantified as a 1.5-fold or greater change relative to control levels. Based on the combined data from proteomic and motif analyses, we hypothesize that five prospective novel kinases (VRK3, GAK, HCK, PKCδ and RSK6) with common functions in inflammatory processes and cellular pathways to regulate apoptosis and the cytoskeleton could serve as potential biomarkers against bacterial propagation in fish. Data from STRING-based functional network analyses indicate that fga is the most central protein. Our collective findings provide new insights into protein phosphorylation patterns, which may serve as effective indicators of A. salmonicida infection in Atlantic salmon.

摘要

嗜水气单胞菌(Aeromonas salmonicida,A. salmonicida)是一种引起疖病的病原菌,对全球经济特别是大西洋鲑(Salmo salar)养殖业构成重大威胁。在之前的研究中,我们鉴定了受到嗜水气单胞菌感染的大西洋鲑肾脏中显著上调的蛋白。进行磷酸化蛋白质组学分析,以进一步阐明细菌感染引发的蛋白质磷酸化模式的动态变化。据我们所知,这是首次对感染嗜水气单胞菌的大西洋鲑中蛋白质的磷酸化事件进行特征描述的研究。总的来说,我们在 3112 种蛋白中鉴定出超过 5635 个磷酸化位点,有 1502 个上调和 77 个下调蛋白的相对定量变化超过 1.5 倍。基于蛋白质组学和基序分析的综合数据,我们假设五个具有共同功能的新型候选激酶(VRK3、GAK、HCK、PKCδ 和 RSK6)在炎症过程和细胞途径中调节细胞凋亡和细胞骨架,可作为鱼类细菌增殖的潜在生物标志物。基于 STRING 的功能网络分析数据表明,fga 是最核心的蛋白。我们的综合研究结果提供了蛋白质磷酸化模式的新见解,这些模式可能成为大西洋鲑感染嗜水气单胞菌的有效指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb7a/6376026/c1e29281886e/41598_2019_38890_Fig1_HTML.jpg

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