畜牧与饲料科学 ›› 2019, Vol. 40 ›› Issue (9): 23-26.doi: 10.12160/j.issn.1672-5190.2019.09.005

• 基础研究 • 上一篇    下一篇

6株猪流行性腹泻病毒N基因的克隆与分析

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

  1. 1.安徽省农业科学院畜牧兽医研究所,安徽 合肥 230031;
    2.安徽省畜禽疫病研究中心,安徽 合肥 230031
  • 收稿日期:2019-07-10 出版日期:2019-09-30 发布日期:2019-12-17
  • 通讯作者: 张丹俊(1962—),男,研究员,主要从事畜禽传染病研究工作。
  • 作者简介:潘孝成(1971—),男,助理研究员,博士,主要从事畜禽传染病研究工作。

Cloning and Sequence Analysis of N Gene of Six Clinical Strains of Porcine Epidemic Diarrhea Virus

PAN Xiao-cheng1, 2, SHEN Xue-huai1, 2, ZHAO Rui-hong1, 2, DAI Yin1, 2, HU Xiao miao1, 2, HOU Hong-yan1, 2, ZHOU Xue-li1, 2, ZHANG Dan-jun1, 2   

  1. 1.Institute of Animal Husbandry and Veterinary Science,Anhui Academy of Agricultural Sciences,Hefei 230031,China;
    2.Livestock and Poultry Epidemic Diseases Research Center of Anhui Province,Hefei 230031,China
  • Received:2019-07-10 Online:2019-09-30 Published:2019-12-17

摘要: 为了解安徽省猪流行性腹泻病毒(PEDV)的遗传变异情况,采用胶体金试纸条检测安徽省境内发生疑似猪流行性腹泻病的病猪粪便(2013—2017年);对PEDV抗原阳性猪样品,利用RT-PCR方法扩增其PEDV N基因,并进行测序和序列分析。结果发现,经胶体金试纸条检测确认了6个猪流行性腹泻发病猪场;对来自该6个猪场的病料样品或病毒传代培养物进行RT-PCR扩增和测序,共获得6株PEDV流行毒株的N基因序列,其序列全长均为1 326 bp,将其分别命名为N12、N22、N32、N42、N52和N62。核苷酸同源性分析显示,6株PEDV分离株N基因之间序列同源性为94.8%~99.8%。其中,5株PEDV分离株(N12、N22、N32、N52和N62)与PEDV疫苗株、经典毒株、2011年之前的我国分离株(LZC、CHS)的同源性较低(94.1%~96.3%),亲缘关系较远;与2011年后国内外PEDV分离株存在较高同源性(96.9%~99.2%),亲缘关系较近;而N42正好相反。该研究表明,近年来安徽各地猪场以PEDV新变异毒株的流行为主。

关键词: 猪流行性腹泻病毒, N基因, 克隆, 序列分析

Abstract: In order to understand the genetic variation of porcine epidemic diarrhea virus(PEDV) in Anhui Province, the fecal samples from pigs with suspected epidemic diarrhea in Anhui province were collected from 2013 to 2017 and were screened for the presence of PEDV antigen by using colloidal gold strip; the PEDV antigen positive samples were subjected to amplification of N gene of PEDV with RT-PCR assay; the obtained sequences were subsequently bioinformatically analyzed. The results showed that the prevalence of porcine epidemic diarrhea was identified in 6 pig farms by colloidal gold strip. RT-PCR amplification and sequencing of the clinical samples or virus passages from the 6 pig farms were carried out, and the N gene sequences of 6 epidemic strains of PEDV were obtained. All of the sequences had a length of 1 326 bp and were designated as N12, N22, N32, N42, N52 and N62, respectively. Nucleotide homology analysis showed that the sequence homology of the N genes among the 6 PEDV isolates ranged from 94.8% to 99.8%. Among them, 5 PEDV isolates (N12, N22, N32, N52 and N62) had low (94.1%~96.3%) homology and non-close genetic relationship with the PEDV vaccine strains, classical strains and Chinese isolates (LZC and CHS) before 2011, whereas had high (96.9%~99.2%) sequence homology and close genetic relationship with the domestic and foreign PEDV strains isolated after 2011. The opposite results were observed in N42. It was indicated that the new variant strains of PEDV were prevalent in pig farms in Anhui province in recent years.

Key words: porcine epidemic diarrhea virus, N gene, cloning, sequence analysis

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