斑点叉尾鮰WNK基因的鉴定及其对鲇鱼肠道败血症的响应

    Identification of WNK gene in channel catfish (Ictalurus punctatus) and its response to ESC

    • 摘要:
      背景 赖氨酸缺乏型蛋白激酶(WNK)是转运、通道和细胞旁蛋白的调节因子,在离子运输过程、维持细胞的渗透压和保持细胞体积的平衡中发挥重要作用。目前尚未有研究对斑点叉尾鮰(Ictalurus punctatus)中WNK基因家族进行系统鉴定和探究其在免疫反应中的作用。
      目的 旨在系统鉴定斑点叉尾鮰WNK基因家族,并探究其在杀鱼爱德华氏菌(Edwardsiella ictaluri)侵染过程中的作用。
      方法 通过生物信息学的方式,利用其他物种的WNK基因家族序列,在斑点叉尾鮰基因组中比对并找到斑点叉尾鮰WNK基因家族序列,通过结构域、系统发育分析,对斑点叉尾鮰的WNK基因家族进行注释确认。利用实时荧光定量聚合酶链式反应(qPCR)分析在杀鱼爱德华氏菌感染后,WNK基因在杀鱼爱德华氏菌易感(YG)和抗性(KX)斑点叉尾鮰群体间的表达模式差异。
      结果 在斑点叉尾鮰中鉴定得到6个WNK基因,分别为WNK1aWNK1bWNK2WNK3WNK4aWNK4b。斑点叉尾鮰在杀鱼爱德华氏菌感染后,除YG48组在24~48 h内死亡的鲇鱼肠道败血症(ESC)易感鱼肠道中的WNK1b外,其他YG组和KX组肝脏和肠道中的WNK1a/b都呈现下调趋势;YG组和KX组肝脏和肠道中的WNK2WNK3WNK4a/b大多呈现显著上调趋势,且YG组的表达量明显高于KX组。
      结论 斑点叉尾鮰肠道和肝脏中的WNK基因参与了ESC疾病过程。本研究结果为抗病性状分子遗传机制的解析提供了参考。

       

      Abstract:
      Background With no lysine kinases (WNK) are regulators of transporters, channels, and paracellular proteins. They play crucial roles in ion transport processes, maintaining cellular osmotic pressure, and regulating cell volume homeostasis. Currently, no studies have conducted systematic identification of the WNK gene family in channel catfish (Ictalurus punctatus) and investigate its role in immune responses.
      Objective This study aims to systematically identify the WNK gene family in channel catfish and investigate their roles during Edwardsiella ictalurid infection.
      Methods Through bioinformatic approaches, the WNK gene family sequences of other species were used to blast against the genome of channel catfish to identify the WNK gene family sequences in channel catfish. The WNK gene family in channel catfish was annotated and confirmed through domain analysis and phylogenetic analysis. Quantitative real-time polymerase chain reaction (qPCR) was employed to analyze the differential expression patterns of WNK genes between E. ictaluri-susceptible (YG group) and -resistant (KX group) channel catfish populations following E. piscicida infection.
      Results Six WNK genes were identified in channel catfish, namely WNK1a, WNK1b, WNK2, WNK3, WNK4a, and WNK4b. After E. ictaluri infection, except for WNK1b in the intestine of the YG48 group Enteric septicaemia of catfish (ESC)-susceptible fish that died within 24−48 hours, WNK1a/b in the liver and intestine of other YG groups and the KX group all showed a down-regulated trend; WNK2, WNK3, and WNK4a/b in the liver and intestine of both YG and KX groups mostly presented a significant up-regulated trend, with the expression levels in the YG group being significantly higher than those in the KX group.
      Conclusion WNK genes in the intestinal and liver of channel catfish are involved in the pathogenesis of ESC. The results of the study provide a reference for analyzing the molecular genetic mechanism of disease-resistant traits.

       

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