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菲律宾蛤仔对褐环病响应的转录变化

Transcriptional changes in Manila clam (Ruditapes philippinarum) in response to Brown Ring Disease.

作者信息

Allam Bassem, Pales Espinosa Emmanuelle, Tanguy Arnaud, Jeffroy Fanny, Le Bris Cedric, Paillard Christine

机构信息

School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, NY, USA.

School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, NY, USA.

出版信息

Fish Shellfish Immunol. 2014 Nov;41(1):2-11. doi: 10.1016/j.fsi.2014.05.022. Epub 2014 Jun 2.

Abstract

Brown Ring Disease (BRD) is a bacterial infection affecting the economically-important clam Ruditapes philippinarum. The disease is caused by a bacterium, Vibrio tapetis, that colonizes the edge of the mantle, altering the biomineralization process and normal shell growth. Altered organic shell matrices accumulate on the inner face of the shell leading to the formation of the typical brown ring in the extrapallial space (between the mantle and the shell). Even though structural and functional changes have been described in solid (mantle) and fluid (hemolymph and extrapallial fluids) tissues from infected clams, the underlying molecular alterations and responses remain largely unknown. This study was designed to gather information on clam molecular responses to the disease and to compare focal responses at the site of the infection (mantle and extrapallial fluid) with systemic (hemolymph) responses. To do so, we designed and produced a Manila clam expression oligoarray (15K Agilent) using transcriptomic data available in public databases and used this platform to comparatively assess transcriptomic changes in mantle, hemolymph and extrapallial fluid of infected clams. Results showed significant regulation in diseased clams of molecules involved in pathogen recognition (e.g. lectins, C1q domain-containing proteins) and killing (defensin), apoptosis regulation (death-associated protein, bcl-2) and in biomineralization (shell matrix proteins, perlucin, galaxin, chitin- and calcium-binding proteins). While most changes in response to the disease were tissue-specific, systemic alterations included co-regulation in all 3 tested tissues of molecules involved in microbe recognition and killing (complement-related factors, defensin). These results provide a first glance at molecular alterations and responses caused by BRD and identify targets for future functional investigations.

摘要

褐环病(BRD)是一种影响具有重要经济价值的菲律宾蛤仔的细菌感染疾病。该疾病由一种细菌——塔氏弧菌引起,这种细菌定殖在鳃的边缘,改变生物矿化过程和正常的贝壳生长。改变的有机贝壳基质在贝壳内表面积累,导致在鳃外空间(在鳃和贝壳之间)形成典型的褐环。尽管已经描述了受感染蛤仔的固体(鳃)和液体(血淋巴和鳃外液体)组织中的结构和功能变化,但潜在的分子改变和反应仍然很大程度上未知。本研究旨在收集蛤仔对该疾病的分子反应信息,并比较感染部位(鳃和鳃外液体)的局部反应与全身(血淋巴)反应。为此,我们利用公共数据库中可用的转录组数据设计并制作了一个菲律宾蛤仔表达寡核苷酸芯片(15K安捷伦),并使用该平台比较评估受感染蛤仔的鳃、血淋巴和鳃外液体中的转录组变化。结果显示,在患病蛤仔中,参与病原体识别(如凝集素、含C1q结构域的蛋白质)、杀伤(防御素)、凋亡调节(死亡相关蛋白、bcl-2)和生物矿化(贝壳基质蛋白、珍珠蛋白、星系蛋白、几丁质和钙结合蛋白)的分子有显著调节。虽然对疾病的大多数反应变化是组织特异性的,但全身改变包括在所有3个测试组织中共同调节参与微生物识别和杀伤的分子(补体相关因子、防御素)。这些结果初步揭示了褐环病引起的分子改变和反应,并确定了未来功能研究的靶点。

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