...
首页> 外文期刊>Archives of virology >Prevalence of equine gammaherpesviruses on breeding farms in Turkey and development of a TaqMan MGB real-time PCR to detect equine herpesvirus 5 (EHV-5)
【24h】

Prevalence of equine gammaherpesviruses on breeding farms in Turkey and development of a TaqMan MGB real-time PCR to detect equine herpesvirus 5 (EHV-5)

机译:火鸡育种农场育种农场的患病率及塔克曼MGB实时PCR检测马疱疹病毒5(EHV-5)

获取原文
获取原文并翻译 | 示例

摘要

Equine herpesvirus type 2 (EHV-2) and EHV-5 are members of the subfamily Gammaherpesvirinae. The viruses are detected in horses with upper respiratory tract disease and are associated with low performance in racehorses. The aim of the current study was to use nested PCR to investigate the epidemiology of EHV-2 and EHV-5 in Arabian horse populations from breeding farms located in three different cities (Eski?ehir, Malatya, and Bursa) in Turkey, using a real-time quantitative PCR (qPCR) with a TaqMan? minor-groove-binder (MGB) probe to detect EHV-5. Screening of blood and ocular and nasal swab samples by nested PCR showed the prevalence of EHV-2 and EHV-5 to be 59 % and 62 %, respectively, with a coinfection rate of 45 %. Thirty-seven isolates from blood samples were identified as EHV-2 using nested PCR. To develop the EHV-5 qPCR, a pair of primers and an MGB probe were designed based on a highly conserved genomic region encoding glycoprotein B (gB). The detection limit of the qPCR was 10 molecules per reaction, and it specifically detected EHV-5 and no other herpesviruses infecting horses (EHV-1, EHV-2, or EHV-4). When applied to field samples, the assay proved to be more sensitive than a well-established nested PCR. Therefore, the qPCR developed in this study provides a rapid, reliable, and sensitive diagnostic assay for the detection of EHV-5, and it complements other diagnostic procedures for equine respiratory disease.
机译:标志性疱疹病毒2型(EHV-2)和EHV-5是亚家族伽马河培育韦里纳的成员。病毒在具有上呼吸道疾病的马匹中检测到,并且与赛马的性能低相关。目前研究的目的是使用巢式PCR来调查阿拉伯马人群的EHV-2和EHV-5的流行病学,从位于土耳其的三个不同城市(Eski?ehir,Malatya和Bursa)的繁殖农场中,使用a与塔克曼的实时定量PCR(QPCR)?次槽粘合剂(MGB)探针检测EHV-5。通过嵌套的PCR筛选血液和眼部和鼻拭子样品,分别呈现EHV-2和EHV-5的患病率分别为59%和62%,共浓度为45%。使用嵌套的PCR鉴定血样的37分离物作为EHV-2。为了开发EHV-5 QPCR,基于编码糖蛋白B(GB)的高度保守的基因组区域设计了一对引物和MGB探针。 QPCR的检测限为每次反应10分子,并且特别检测到EHV-5,没有其他疱疹病毒感染马(EHV-1,EHV-2或EHV-4)。当施加到场样品时,检测结果被证明比建立良好的嵌套PCR更敏感。因此,本研究开发的QPCR为检测到EHV-5提供了一种快速,可靠和敏感的诊断测定,并补充了马呼吸道疾病的其他诊断程序。

著录项

  • 来源
    《Archives of virology 》 |2014年第11期| 共7页
  • 作者单位

    Department of Virology Ankara University DiskapiAnkara Turkey;

    Institut für Virologie Zentrum für Infektionsmedizin Robert von Ostertag-Haus Freie Universit?t;

    Institut für Virologie Zentrum für Infektionsmedizin Robert von Ostertag-Haus Freie Universit?t;

    Institut für Virologie Zentrum für Infektionsmedizin Robert von Ostertag-Haus Freie Universit?t;

    Institut für Virologie Zentrum für Infektionsmedizin Robert von Ostertag-Haus Freie Universit?t;

    Department of Virology Ankara University DiskapiAnkara Turkey;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学微生物学(病原细菌学、病原微生物学) ;
  • 关键词

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