Department of Fisheries and Allied Aquacultures, Aquatic Genomics Unit, Auburn University, Auburn, AL 36849, USA.
Fish Shellfish Immunol. 2012 May;32(5):816-27. doi: 10.1016/j.fsi.2012.02.004. Epub 2012 Feb 17.
The mucosal surfaces of fish (gill, skin, gastrointestinal tract) are important sites of bacterial exposure and host defense mechanisms. In mammalian systems, the intestinal epithelium is well characterized as both a selectively permeable barrier regulated by junctional proteins and as a primary site of infection for a number of enteric pathogens including viruses, bacteria, and parasites. The causative bacterium of enteric septicemia of catfish, Edwardsiella ictaluri, is believed to gain entry through the intestinal epithelium, with previous research using a rat intestinal epithelial cell line (IEC-6) indicating actin polymerization and receptor-mediated endocytosis as potential mechanisms of uptake. Here, we utilized high-throughput RNA-seq to characterize the role of the intestinal epithelial barrier following E. ictaluri challenge. A total of 197.6 million reads were obtained and assembled into 176,481 contigs with an average length of 893.7 bp and N50 of 1676 bp. The assembled contigs contained 14,457 known unigenes, including 2719 genes not previously identified in other catfish transcriptome studies. Comparison of digital gene expression between challenged and control samples revealed 1633 differentially expressed genes at 3 h, 24 h, and 3 day following exposure. Gene pathway analysis of the differentially expressed gene set indicated the centrality of actin cytoskeletal polymerization/remodelling and junctional regulation in pathogen entry and subsequent inflammatory responses. The expression patterns of fifteen differentially expressed genes related to intestinal epithelial barrier dysfunction were validated by quantitative real-time RT-PCR (average correlation coeff. 0.92, p < 0.001). Our results set a foundation for future studies comparing mechanisms of pathogen entry and mucosal immunity across several important catfish pathogens including E. ictaluri, Edwardsiellatarda, Flavobacterium columnare, and virulent atypical Aeromonas hydrophila. Understanding of molecular mechanisms of pathogen entry during infection will provide insight into strategies for selection of resistant catfish brood stocks against various diseases.
鱼类(鳃、皮肤、胃肠道)的黏膜表面是细菌暴露和宿主防御机制的重要部位。在哺乳动物系统中,肠道上皮被很好地描述为具有选择性渗透性的屏障,由连接蛋白调节,并且是许多肠道病原体(包括病毒、细菌和寄生虫)感染的主要部位。鲶鱼败血病的病原体爱德华氏菌(Edwardsiella ictaluri)被认为是通过肠道上皮进入的,之前使用大鼠肠道上皮细胞系(IEC-6)的研究表明,肌动蛋白聚合和受体介导的内吞作用是摄取的潜在机制。在这里,我们利用高通量 RNA-seq 来描述爱德华氏菌(E. ictaluri)感染后肠道上皮屏障的作用。共获得 1.976 亿条reads,并组装成 176481 个 contigs,平均长度为 893.7 bp,N50 为 1676 bp。组装的 contigs包含 14457 个已知的 unigenes,包括在其他鲶鱼转录组研究中未鉴定出的 2719 个基因。对实验组和对照组之间的数字基因表达进行比较,发现暴露后 3 小时、24 小时和 3 天有 1633 个差异表达基因。差异表达基因集的基因途径分析表明,肌动蛋白细胞骨架聚合/重塑和连接调节在病原体进入和随后的炎症反应中具有核心地位。15 个与肠道上皮屏障功能障碍相关的差异表达基因的表达模式通过定量实时 RT-PCR 进行了验证(平均相关系数 0.92,p < 0.001)。我们的研究结果为未来的研究奠定了基础,这些研究将比较包括爱德华氏菌(E. ictaluri)、迟缓爱德华氏菌(Edwardsiellatarda)、柱状黄杆菌(Flavobacterium columnare)和强毒非典型嗜水气单胞菌(virulent atypical Aeromonas hydrophila)在内的几种重要鲶鱼病原体的病原体进入和黏膜免疫机制。对感染过程中病原体进入的分子机制的了解将为选择各种疾病抗性鲶鱼苗种提供策略。