首页> 外文期刊>Frontiers in Veterinary Science >Viral Enrichment Methods Affect the Detection but Not Sequence Variation of West Nile Virus in Equine Brain Tissue
【24h】

Viral Enrichment Methods Affect the Detection but Not Sequence Variation of West Nile Virus in Equine Brain Tissue

机译:病毒富集方法影响马脑组织中西尼罗河病毒的检测但不影响序列变异

获取原文
获取外文期刊封面目录资料

摘要

West Nile virus (WNV), a small, positive sense, single stranded RNA virus continues to encroach into new locales with emergence of new viral variants. Neurological disease in the equine can be moderate to severe in the face of low to undetectable virus loads. Physical methods of virus enrichment may increase sensitivity of virus detection and enhance analysis of viral diversity, especially for deep sequencing studies. However, the use of these techniques is limited mainly to non-neural tissues. We investigated the hypothesis that elimination of equine brain RNA enhances viral detection without limiting viral variation. Eight different WNV viral RNA enrichment and host RNA separation methods were evaluated to determine if elimination of host RNA enhanced detection of WNV and increase the repertoire of virus variants for sequencing. Archived brain tissue from 21 different horses was inoculated with WNV, homogenized, before enrichment and separation. The protocols utilized combinations of low-speed centrifugation, syringe filtration, and nuclease treatment. Viral and host RNA were analyzed using real-time PCR targeting the WNV Envelope (E) protein and equine G3PDH to determine relative sensitivity for WNV and host depletion, respectively. To determine the effect of these methods on viral variation, deep sequencing of the E protein was performed. Our results demonstrate that additional separation and enrichment methods resulted in loss of virus in the face of host RNA depletion. DNA sequencing showed no significant difference in total sequence variation between the RNA enrichment protocols. For equine brain infected with WNV, direct RNA extraction followed by host RNA depletion was most suitable. This study highlights the importance of evaluating viral enrichment and separation methods according to tissue type before embarking on studies where quantification of virus and viral variants is essential to the outcome of the study.
机译:西尼罗河病毒(WNV)是一种小巧的阳性单链RNA病毒,随着新病毒变种的出现,继续侵入新的地区。面对低至无法检测的病毒载量,马的神经系统疾病可能为中度至重度。富集病毒的物理方法可能会提高病毒检测的敏感性,并增强对病毒多样性的分析,尤其是对于深度测序研究而言。但是,这些技术的使用主要限于非神经组织。我们调查的假说,消除马脑RNA可以增强病毒检测而不会限制病毒变异。评估了八种不同的WNV病毒RNA富集和宿主RNA分离方法,以确定消除宿主RNA是否增强WNV的检测并增加用于测序的病毒变体库。在富集和分离之前,将21匹不同马的存档脑组织接种WNV,均质化。该协议利用了低速离心,注射器过滤和核酸酶处理的组合。使用针对WNV包膜(E)蛋白和马G3PDH的实时PCR分析病毒和宿主RNA,分别确定WNV和宿主耗竭的相对敏感性。为了确定这些方法对病毒变异的影响,对E蛋白进行了深度测序。我们的结果表明,面对宿主RNA消耗,其他分离和富集方法会导致病毒损失。 DNA测序显示RNA富集方案之间的总序列变异无显着差异。对于感染了WNV的马脑,最合适的方法是直接提取RNA,然后去除宿主RNA。这项研究强调了在着手进行病毒和病毒变异的量化对于研究结果至关重要的研究之前,根据组织类型评估病毒富集和分离方法的重要性。

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