中国畜牧兽医 ›› 2020, Vol. 47 ›› Issue (12): 4051-4058.doi: 10.16431/j.cnki.1671-7236.2020.12.029

• 预防兽医 • 上一篇    下一篇

仔猪小肠上皮细胞的体外培养及猪流行性腹泻病毒对其感染性研究

沈学怀1, 翟银建2, 尹磊1, 潘孝成1, 张丹俊1, 赵瑞宏1, 戴银1, 胡晓苗1, 周学利1, 侯宏艳1   

  1. 1. 安徽省农业科学院畜牧兽医研究所, 安徽省畜禽疫病研究中心, 畜禽产品安全工程安徽省重点实验室, 合肥 230031;
    2. 阜南县农业农村局, 阜南 236300
  • 收稿日期:2020-07-09 出版日期:2020-12-20 发布日期:2020-12-18
  • 通讯作者: 潘孝成 E-mail:pxcpyq@sina.com
  • 作者简介:沈学怀(1986-),男,安徽凤阳人,硕士,研究方向:畜禽传染病,E-mail:xuehuaishen1986@126.com
  • 基金资助:
    国家现代农业产业技术体系项目(CARS-41);安徽省重点研究与开发计划项目(1704a07020066)

Culture of Piglet Intestinal Epithelial Cells in vitro and the Infectivity of Porcine Epidemic Diarrhea Virus on the Cells

SHEN Xuehuai1, ZHAI Yinjian2, YIN Lei1, PAN Xiaocheng1, ZHANG Danjun1, ZHAO Ruihong1, DAI Yin1, HU Xiaomiao1, ZHOU Xueli1, HOU Hongyan1   

  1. 1. Anhui Province Key Laboratory of Livestock and Poultry Product Safety Engineering, Livestock and Poultry Epidemic Diseases Research Center of Anhui Province, Institute of Animal and Veterinary Science, Anhui Academy of Agricultural Sciences, Hefei 230031, China;
    2. Agricultural and Rural Bureau of Funan County, Funan 236300, China
  • Received:2020-07-09 Online:2020-12-20 Published:2020-12-18

摘要: 本研究旨在建立一种操作简单的仔猪小肠上皮细胞体外培养体系,为猪流行性腹泻病毒(porcine epidemic diarrhea virus,PEDV)的相关研究提供材料。研究以未吃初乳的新生仔猪作为肠道供体,采用肠腔面刮取肠黏膜和机械分离分散的方式进行原代细胞的体外分离。采用0.1%胰蛋白酶差速消化法进行仔猪小肠上皮细胞的纯化;比较新生弱仔猪和正常仔猪作为供体对原代小肠上皮细胞活性的影响;MTT法比较不同代次原代细胞的增殖活性;免疫荧光和实时荧光定量RT-PCR方法检测PEDV毒株CV777在原代小肠上皮细胞感染和增殖情况。结果显示,本研究建立的体外分离培养方法能获得增殖活性良好的原代小肠上皮细胞,具有明显的"S"型细胞增殖曲线。通过胰酶差速消化可得到纯度高、形态单一的小肠上皮细胞,同时细胞连续传代5次仍保持良好的增殖活性。弱仔猪和正常仔猪分离培养的小肠上皮细胞的增殖活性比较显示,两者并没有明显区别,这为降低原代细胞培养的成本提供新的思路。免疫荧光和实时荧光定量RT-PCR结果显示,PEDV可感染本方法分离培养的仔猪原代小肠上皮细胞,并在其中进行复制增殖。本研究建立了一种操作简单、实用性强、成本较低的仔猪原代小肠上皮细胞体外培养方法,该方法培养的原代细胞可作为PEDV分离培养和相关研究的基础材料。

关键词: 仔猪小肠上皮细胞; 体外培养; 猪流行性腹泻病毒(PEDV); 增殖活性; 细胞传代

Abstract: The study was aimed to establish a simple in vitro culture system for piglet small intestinal epithelial cells,and to provide materials for researches on porcine epidemic diarrhea virus (PEDV).In this study,newborn piglets that did not eat colostrum were used as the initial donors,and the primary cells were separated in vitro by scraping the intestinal mucosa from the intestinal lumen and mechanical separation and dispersion.The piglet intestinal epithelial cells were purified using 0.1% trypsin differential digestion method.Compared the effects of newborn weak piglets and normal piglets as donors on the activity of primary intestinal epithelial cells.MTT method was used to compare the proliferation activity of primary cells of different generations.Immunofluorescence and Real-time RT-PCR were used to detect the infection and proliferation of PEDV strain CV777 in primary intestinal epithelial cells.The results showed that the isolation and culture method in vitro used in this study could obtain primary intestinal epithelial cells with good proliferation activity,with obvious S-type cell proliferation curves.The cells with high purity and single morphology could be obtained by differential digestion,and had good proliferation activity after five consecutive passages.The proliferative activity of intestinal epithelial cells isolated from weak piglets and normal piglets had no obvious difference,and provided new way for reducing the cost of primary cell culture.The results of immunofluorescence and Real-time RT-PCR showed that PEDV could infect the primary intestinal epithelial cells,and replicated and proliferated in them.In this study,we established a simple,practical and low-cost method for in vitro culture of piglet primary small intestinal epithelial cells.The primary cells cultured by this method could be used as basic materials for the isolation and culture of PEDV and related research.

Key words: piglet intestinal epithelial cells; in vitro culture; porcine epidemic diarrhea virus (PEDV); proliferative activity; cell passage

中图分类号: