中国农业科学 ›› 2008, Vol. 41 ›› Issue (3): 861-867 .doi: 10.3864/j.issn.0578-1752.2008.03.032

• 兽医 • 上一篇    下一篇

鸡气管上皮细胞分离培养及传支病毒在其培养特性研究

孙 裴,张彦明,张 浩,高春生,张为民,王晶钰,郭抗抗,党如意   

  1. 西北农林科技大学动物医学院
  • 收稿日期:2007-08-30 修回日期:1900-01-01 出版日期:2008-03-10 发布日期:2008-03-10
  • 通讯作者: 张彦明

Research of Dissociation Culture of Chicken Trachea-bronchia Epithelium and Culture Characteristics of IBV in the Epithelium

  

  1. 西北农林科技大学动物医学院
  • Received:2007-08-30 Revised:1900-01-01 Online:2008-03-10 Published:2008-03-10

摘要: 【目的】探索鸡气管上皮细胞(chicken trachea epithelium,CTE)分离培养技术,并研究传染性支气管炎病毒(infectious bronchitis virus,IBV)在CTE中培养特性。【方法】利用气管灌注冷消化法分离培养CTE,对CTE特异性8/18角蛋白作免疫组化鉴定上皮细胞。培养的CTE分别接种IBV M41株和T株,分别在接种后第12~96小时观察接毒细胞形态学变化,应用电镜技术观察CTE细胞病变和病毒粒子结构,利用RT-PCR技术检测CTE中病毒核酸并对CTE中IBV的血凝性和鸡胚致病性进行检测。【结果】利用灌注冷消化法可以获得形态完整并带有纤毛的CTE,细胞活性高,经过3步纯化后的CTE均一性高、生长快。两株IBV感染的CTE分别在接毒72和84 h后产生明显的细胞病变效应(cytopathic effect,CPE),血凝性和致鸡胚病变检测结果呈阳性。【结论】本研究成功分离培养了CTE,可以为CTE相关研究提供技术支持,并为IBV基础研究和应用奠定基础。

关键词: 鸡气管上皮细胞, 分离, 培养, IBV, 培养特性

Abstract: [Objective] The purpose of this study was to explore and find out appropriate technology of separation and culture for chicken trachea-bronchia epithelium and also to research culture characteristics of IBV in chicken trachea-bronchia epithelium. [Method] By the method of douche, chicken trachea-bronchia epithelium was digested overnight at 4℃ and separated. Then the test of immunohistochemistry of No.8/18 keratins of chicken trachea-bronchia epithelium was done to identify epithelium. The cultured epithelium was infected respectively by IBV-M41 strain(Style Breath ) and IBV-T strain(Style Kidney), and respectively at 12,24,32,48,60,72,84 and 96h after epithelium infected by IBV we observed morphologic changes of epithelium. At last the method of RT-PCR was used to detect IBV mRNA in each group of cells. At the same time the ability of haemagglutination and pathological changes of chicken embryo caused by IBV were tested. [Result] By the method of douche and digestion overnight chicken trachea-bronchia epithelium have been separated and have full morphologic structure and clearly visible cilia and high livingness. Through three-step purification the epithelium has good uniformity and grow faster. Respectively at 72h and 84h after each IBV strain and its corresponding epithelium co-culture, the infected epithelium appeared obvious cell pathologic effect(CPE), and the test of ability of haemagglutination and pathological changes of chicken embryo by IBV were both positive. [Conclusion] We have successfully separated and cultured chicken trachea-bronchia epithelium to fulfill the need of relative deeper research by providing chicken trachea-bronchia epithelium as research model. And both IBV-M41 strain and IBV-T strain may cause chicken trachea-bronchia epithelium to appear CPE, which provide nicer bases for future relative research about IBV laboratory diagnosis, medicine sensitivity test and pathology mechanism caused by IBV.

Key words: Chicken trachea-bronchia, Epithelium, Dissociation culture, IBV, Culture characteristics