School of Life Sciences, Key Laboratory for Biotechnology on Medicinal Plants of Jiangsu Province, Jiangsu Normal University, Xuzhou 221116, China.
School of Life Sciences, Key Laboratory for Biotechnology on Medicinal Plants of Jiangsu Province, Jiangsu Normal University, Xuzhou 221116, China.
Fish Shellfish Immunol. 2014 Jan;36(1):229-39. doi: 10.1016/j.fsi.2013.11.007. Epub 2013 Nov 21.
The gills are large mucosal surfaces and very important portals for pathogen entry in fish. The aim of this study was to determine the gill immune response at the protein levels, the differential proteomes of the zebrafish gill response to Aeromonas hydrophila infection were identified with isobaric tags for relative and absolute quantitation (iTRAQ) labeling followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). A total of 1338 proteins were identified and classified into the categories primarily related to cellular process (15.36%), metabolic process (11.95%) and biological regulation (8.29%). Of these, 82 differentially expressed proteins were reliably quantified by iTRAQ analysis, 57 proteins were upregulated and 25 proteins were downregulated upon bacterial infection. Gene ontology (GO) enrichment analysis showed that approximately 33 (8.8%) of the differential proteins in gills were involved in the stress and immune responses. Several upregulated proteins were observed such as complement component 5, serpin peptidase inhibitor clade A member 7, annexin A3a, histone H4, glyceraldehyde 3-phosphate dehydrogenase, creatine kinase, and peroxiredoxin. These protein expression changes were further validated at the transcript level using microarray analysis. Moreover, complement and coagulation cascades, pathogenic Escherichia coli infection and phagosome were the significant pathways identified by KEGG enrichment analysis. This is first report on proteome of fish gills against A. hydrophila infection, which contribute to understanding the defense mechanisms of the gills in fish.
鱼的鳃是大型黏膜表面,是病原体进入鱼体的重要门户。本研究旨在从蛋白质水平上确定鳃的免疫反应,采用相对和绝对定量同位素标记(iTRAQ)标记后进行液相色谱-串联质谱(LC-MS/MS),鉴定斑马鱼鳃对嗜水气单胞菌感染的差异蛋白质组。共鉴定出 1338 种蛋白质,并分为与细胞过程(15.36%)、代谢过程(11.95%)和生物调节(8.29%)相关的主要类别。其中,82 种差异表达蛋白通过 iTRAQ 分析可靠定量,57 种蛋白上调,25 种蛋白下调。基因本体(GO)富集分析表明,鳃中约 33 种(8.8%)差异蛋白参与应激和免疫反应。观察到几种上调蛋白,如补体成分 5、丝氨酸蛋白酶抑制剂 A7 成员、膜联蛋白 A3a、组蛋白 H4、甘油醛 3-磷酸脱氢酶、肌酸激酶和过氧化物酶。这些蛋白表达变化进一步通过微阵列分析在转录水平上进行验证。此外,补体和凝血级联、致病性大肠杆菌感染和吞噬体是通过 KEGG 富集分析鉴定的重要途径。这是首次报道鱼类鳃针对嗜水气单胞菌感染的蛋白质组,有助于了解鱼类鳃的防御机制。