首页> 外文期刊>BMC Veterinary Research >Characterization of ovine hepatic gene expression profiles in response to Escherichia coli lipopolysaccharide using a bovine cDNA microarray
【24h】

Characterization of ovine hepatic gene expression profiles in response to Escherichia coli lipopolysaccharide using a bovine cDNA microarray

机译:使用牛cDNA微阵列表征响应大肠杆菌脂多糖的绵羊肝基因表达谱

获取原文
           

摘要

Background During systemic gram-negative bacterial infections, lipopolysaccharide (LPS) ligation to the hepatic Toll-like receptor-4 complex induces the production of hepatic acute phase proteins that are involved in the host response to infection and limit the associated inflammatory process. Identifying the genes that regulate this hepatic response to LPS in ruminants may provide insight into the pathogenesis of bacterial diseases and eventually facilitate breeding of more disease resistant animals. The objective of this research was to profile the expression of ovine hepatic genes in response to Escherichia coli LPS challenge (0, 200, 400 ng/kg) using a bovine cDNA microarray and quantitative real-time PCR (qRT-PCR). Results Twelve yearling ewes were challenged iv with E. coli LPS (0, 200, 400 ng/kg) and liver biopsies were collected 4–5 hours post-challenge to assess hepatic gene expression profiles by bovine cDNA microarray and qRT-PCR analyses. The expression of CD14 , C3 , IL12R, NRAMP1 , SOD and IGFBP3 genes was down regulated, whereas the expression of ACTHR , IFNαR , CD1 , MCP-1 and GH was increased during LPS challenge. With the exception of C3, qRT-PCR analysis of 7 of these genes confirmed the microarray results and demonstrated that GAPDH is not a suitable housekeeping gene in LPS challenged sheep. Conclusion We have identified several potentially important genes by bovine cDNA microarray and qRT-PCR analyses that are differentially expressed during the ovine hepatic response to systemic LPS challenge. Their potential role in regulating the inflammatory response to LPS warrants further investigation.
机译:背景技术在全身革兰氏阴性细菌感染期间,脂多糖(LPS)与肝Toll样受体4复合物的连接可诱导肝急性期蛋白的产生,这些蛋白参与宿主对感染的反应并限制了相关的炎症过程。鉴定调节反刍动物中肝脏对LPS的这种反应的基因可能提供细菌疾病发病机理的见解,并最终促进更多抗病动物的繁殖。这项研究的目的是使用牛cDNA微阵列和定量实时PCR(qRT-PCR)分析响应大肠杆菌LPS攻击(0、200、400 ng / kg)的绵羊肝基因的表达。结果用大肠杆菌LPS(0、200、400 ng / kg)对十二岁的一头母羊进行静脉内攻击,并在攻击后4-5小时收集肝脏活检样品,以通过牛cDNA微阵列和qRT-PCR分析评估肝脏基因表达谱。在LPS攻击期间,CD14,C3,IL12R,NRAMP1,SOD和IGFBP3基因的表达下调,而ACTHR,IFNαR,CD1,MCP-1和GH的表达增加。除C3外,对其中7个基因的qRT-PCR分析证实了微阵列结果,并证明GAPDH不是LPS攻击绵羊的合适管家基因。结论我们通过牛cDNA芯片和qRT-PCR分析鉴定了几个潜在重要基因,这些基因在绵羊肝对系统性LPS攻击的反应中差异表达。它们在调节对LPS的炎症反应中的潜在作用值得进一步研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号