Nadin-Davis Susan A, Colville Adam, Trewby Hannah, Biek Roman, Real Leslie
Animal Health Microbiology Research, Ottawa Laboratory Fallowfield, Canadian Food Inspection Agency, Ottawa, Ontario, Canada.
Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, Scotland, UK.
Virus Res. 2017 Mar 15;232:123-133. doi: 10.1016/j.virusres.2017.02.007. Epub 2017 Feb 17.
Raccoon rabies remains a serious public health problem throughout much of the eastern seaboard of North America due to the urban nature of the reservoir host and the many challenges inherent in multi-jurisdictional efforts to administer co-ordinated and comprehensive wildlife rabies control programmes. Better understanding of the mechanisms of spread of rabies virus can play a significant role in guiding such control efforts. To facilitate a detailed molecular epidemiological study of raccoon rabies virus movements across eastern North America, we developed a methodology to efficiently determine whole genome sequences of hundreds of viral samples. The workflow combines the generation of a limited number of overlapping amplicons covering the complete viral genome and use of high throughput sequencing technology. The value of this approach is demonstrated through a retrospective phylogenetic analysis of an outbreak of raccoon rabies which occurred in the province of Ontario between 1999 and 2005. As demonstrated by the number of single nucleotide polymorphisms detected, whole genome sequence data were far more effective than single gene sequences in discriminating between samples and this facilitated the generation of more robust and informative phylogenies that yielded insights into the spatio-temporal pattern of viral spread. With minor modification this approach could be applied to other rabies virus variants thereby facilitating greatly improved phylogenetic inference and thus better understanding of the spread of this serious zoonotic disease. Such information will inform the most appropriate strategies for rabies control in wildlife reservoirs.
浣熊狂犬病在北美东海岸大部分地区仍然是一个严重的公共卫生问题,这是由于储存宿主的城市特性以及在多辖区开展协调一致且全面的野生动物狂犬病控制计划时所面临的诸多挑战。更好地了解狂犬病病毒的传播机制对于指导此类控制工作可发挥重要作用。为便于对浣熊狂犬病病毒在北美东部的传播进行详细的分子流行病学研究,我们开发了一种方法,能够高效确定数百个病毒样本的全基因组序列。该工作流程结合了生成覆盖完整病毒基因组的有限数量重叠扩增子以及使用高通量测序技术。通过对1999年至2005年安大略省发生的一次浣熊狂犬病疫情进行回顾性系统发育分析,证明了这种方法的价值。正如所检测到的单核苷酸多态性数量所示,全基因组序列数据在区分样本方面远比单基因序列有效,这有助于生成更可靠且信息丰富的系统发育树,从而深入了解病毒传播的时空模式。只需进行微小修改,这种方法就可应用于其他狂犬病病毒变种,从而极大地促进系统发育推断的改进,进而更好地了解这种严重人畜共患病的传播情况。此类信息将为野生动物储存宿主中狂犬病控制的最合适策略提供依据。