VVD Program, The Pirbright Institute, Pirbright, Surrey, United Kingdom.
PLoS One. 2013;8(3):e57747. doi: 10.1371/journal.pone.0057747. Epub 2013 Mar 8.
The recent unprecedented emergence of arboviruses transmitted by Culicoides biting midges in northern Europe has necessitated the development of techniques to differentiate competent vector species. At present these techniques are entirely reliant upon interpretation of semi-quantitative RT-PCR (sqPCR) data in the form of Cq values used to infer the presence of viral RNA in samples.
METHODOLOGY/PRINCIPAL FINDINGS: This study investigates the advantages and limitations of sqPCR in this role by comparing infection and dissemination rates of Schmallenberg virus (SBV) in two colony lines of Culicoides. Through the use of these behaviorally malleable lines we provide tools for demarcating arbovirus infection and dissemination rates in Culicoides which to date have prevented clear implication of primary vector species in northern Europe. The study demonstrates biological transmission of SBV in an arthropod vector, supporting the conclusions from field-caught Culicoides and provides a general framework for future assessment of vector competence of Culicoides for arboviruses using sqPCR.
CONCLUSIONS/SIGNIFICANCE: When adopting novel diagnostic technologies, correctly implicating vectors of arboviral pathogens requires a coherent laboratory framework to fully understand the implications of results produced in the field. This study illustrates these difficulties and provides a full examination of sqPCR in this role for the Culicoides-arbovirus system.
最近,在北欧通过蠓传播的虫媒病毒的空前出现,使得开发技术来区分有能力的媒介物种成为必要。目前,这些技术完全依赖于对 Cq 值的半定量 RT-PCR(sqPCR)数据的解释,这些数据用于推断样本中病毒 RNA 的存在。
方法/主要发现:本研究通过比较两种库蠓(Culicoides)品系中沙姆布鲁病毒(SBV)的感染和传播率,调查了 sqPCR 在这一角色中的优势和局限性。通过使用这些行为上可塑的品系,我们提供了在库蠓中划分虫媒病毒感染和传播率的工具,这些工具迄今为止一直阻止了在北欧确定主要媒介物种的明确作用。该研究在节肢动物媒介中证明了 SBV 的生物传播,支持了从野外捕获的库蠓得出的结论,并为使用 sqPCR 评估库蠓对虫媒病毒的媒介能力提供了一个通用框架。
结论/意义:当采用新型诊断技术时,正确地暗示虫媒病毒病原体的媒介需要一个连贯的实验室框架,以充分理解在野外产生的结果的含义。本研究说明了这些困难,并对 Culicoides-arbovirus 系统中的 sqPCR 进行了全面检查。