Bastos A D S, Arnot L F, Jacquier M D, Maree S
Mammal Research Institute, Department of Zoology and Entomology, University of Pretoria, Pretoria 0002, South Africa.
Med Vet Entomol. 2009 Dec;23(4):399-409. doi: 10.1111/j.1365-2915.2009.00828.x.
African swine fever virus (ASFV) infection in adult Ornithodoros porcinus (Murry 1877, sensuWalton 1979) ticks collected from warthog burrows in southern and East Africa was assessed using a duplex genomic amplification approach that is informative with respect to the invertebrate host species and infecting sylvatic cycle virus. DNA extracted from individual ticks was used as template for the simultaneous amplification of a C-terminal 478-bp ASFV p72 gene region and a approximately 313-bp fragment of the tick mitochondrial 16S rRNA gene, under optimized reaction conditions. Within-warthog burrow infection rates ranged from 0% to 43% using this approach, and phylogenetic analysis of 16S gene sequences revealed the presence of three geographically discrete O. porcinus lineages, but no support for subspecies recognition. False negatives are precluded by the inclusion of host species-informative primers that ensure the DNA integrity of cytoplasmically located genome extracts. In addition, infection rate estimates are further improved as false positives arising from carry-over contamination when performing a two-step nested polymerase chain reaction are negated by the one-step approach. Phylogenetic comparison of full-length virus gene sequences with the partial C-terminal p72 gene target confirmed the epidemiological utility of the latter in a sylvatic setting. The method is therefore of particular value in studies assessing the prevalence and diversity of ASFV in relation to the African sylvatic tick vector and holds potential for investigating the role of alternative tick species in virus maintenance and transmission.
利用一种双重基因组扩增方法,对从非洲南部和东部疣猪洞穴采集的成年非洲钝缘蜱(奥氏钝缘蜱,Murry 1877,根据Walton 1979的分类)感染非洲猪瘟病毒(ASFV)的情况进行了评估,该方法对于无脊椎动物宿主物种和感染的野生病毒循环具有信息价值。在优化的反应条件下,从单个蜱虫中提取的DNA用作模板,同时扩增ASFV p72基因C端478bp区域和蜱虫线粒体16S rRNA基因约313bp的片段。采用这种方法,疣猪洞穴内的感染率在0%至43%之间变化,对16S基因序列的系统发育分析揭示了存在三个地理上离散的奥氏钝缘蜱谱系,但不支持亚种识别。通过加入确保细胞质定位基因组提取物DNA完整性的宿主物种信息引物,可避免假阴性。此外,由于一步法消除了两步巢式聚合酶链反应中因残留污染产生的假阳性,感染率估计值得到了进一步提高。将全长病毒基因序列与部分C端p72基因靶点进行系统发育比较,证实了后者在野生环境中的流行病学效用。因此,该方法在评估与非洲野生蜱传播媒介相关的ASFV流行率和多样性的研究中具有特别价值,并且在研究替代蜱物种在病毒维持和传播中的作用方面具有潜力。