首页> 外文期刊>Animal Science Journal >Propagation of bovine coronavirus in clones of the Caco-2 cell line showing different levels of alkaline phosphatase activity.
【24h】

Propagation of bovine coronavirus in clones of the Caco-2 cell line showing different levels of alkaline phosphatase activity.

机译:牛冠状病毒在Caco-2细胞系克隆中的繁殖,显示出不同水平的碱性磷酸酶活性。

获取原文
获取原文并翻译 | 示例
           

摘要

The aim of the present study was to determine whether bovine coronavirus (BCV) has the ability to initiate infection in a human colon carcinoma cell line, Caco-2, that has been established to spontaneously differentiate after confluence. When Caco-2 cells were infected with BCV, a titre of 5.5x106 plaque-forming units (p.f.u.)/ml was found in the culture supernatant at 5 days postinfection. Two clones, Caco-2/CA1 and Caco-2/CA2, were then isolated by monitoring alkaline phosphatase (ALP) and cell proliferation activities. The ALP activity level of CA1 cells was significantly higher than that of CA2 cells, while the level of cell proliferation activity of CA1 was significantly lower than that of CA2. When CA1 and CA2 cells were infected with BCV at confluence, virus haemagglutination (HA) was detected in the culture supernatant at 5 days postinfection for CA1 cells and at 8 days postinfection for CA2 cells. Thus, BCV propagation was substantially delayed in CA2 cells, suggesting that a cellular factor(s) that appears at the differentiation stage may control BCV propagation. BCV-susceptible CA1 and CA2 cells showing different levels of ALP activity would be useful for further experiments to elucidate the mechanism of BCV propagation..
机译:本研究的目的是确定牛冠状病毒(BCV)是否具有启动人结肠癌细胞系Caco-2感染的能力,该细胞系已建立以在融合后自发分化。当BCV感染Caco-2细胞时,感染后5天在培养上清液中发现滴度为5.5x106噬菌斑形成单位(p.f.u。)/ ml。然后通过监测碱性磷酸酶(ALP)和细胞增殖活性,分离出两个克隆Caco-2 / CA1和Caco-2 / CA2。 CA1细胞的ALP活性水平显着高于CA2细胞,而CA1的细胞增殖活性水平显着低于CA2。在汇合时用BCV感染CA1和CA2细胞时,对于CA1细胞,在感染后5天和对于CA2细胞,在感染后8天时,在培养上清液中检测到病毒血细胞凝集(HA)。因此,BCV传播在CA2细胞中被大大延迟,表明在分化阶段出现的细胞因子可以控制BCV传播。表现出不同水平的ALP活性的BCV易感性BC1和CA2细胞可用于进一步的实验,以阐明BCV传播的机制。

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