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A host species-informative internal control for molecular assessment of African swine fever virus infection rates in the African sylvatic cycle Ornithodoros vector.

机译:用于对非洲sylvatic循环 Ornithodoros 载体中非洲猪瘟病毒感染率进行分子评估的宿主物种信息内部控制。

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African swine fever virus (ASFV) infection in adult Ornithodoros porcinus (Murry 1877, sensu Walton 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 ~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.
机译:使用双重基因组评估了从南部和东部非洲的疣猪洞穴采集的成年 Ornithodoros porcinus (Murry 1877, sensu Walton 1979)成年非洲猪瘟病毒(ASFV)感染扩增方法,对无脊椎动物宿主物种和感染sylvatic循环病毒很有帮助。在优化的条件下,将从各个template中提取的DNA用作模板,同时扩增tick线粒体16S rRNA基因的C端478-bp ASFV p 72基因区域和〜313-bp片段反应条件。使用这种方法,疣猪内的洞穴内感染率在0%到43%之间,并且对16S基因序列的系统发育分析表明存在3个地理上离散的i。猪谱系,但不支持亚种识别。假阴性的排除是通过包含能确保细胞质定位的基因组提取物的DNA完整性的宿主物种信息性引物。另外,通过一步法消除了进行两步嵌套式聚合酶链反应时由于残留污染引起的假阳性,感染率估计值得到进一步改善。系统发育比较全长病毒基因序列与部分C末端 p 72基因靶标,证实了后者在流行环境中的流行病学效用。因此,该方法在评估ASFV相对于非洲的tick虫媒介的流行和多样性的研究中特别有价值,并具有研究替代potential种在病毒维持和传播中的作用的潜力。

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