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首页> 外文期刊>Journal of Clinical Microbiology >Molecular Detection, Epidemiology, and Genetic Characterization of Novel European Field Isolates of Equine Infectious Anemia Virus
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Molecular Detection, Epidemiology, and Genetic Characterization of Novel European Field Isolates of Equine Infectious Anemia Virus

机译:马传染性贫血病毒的新型欧洲现场分离株的分子检测,流行病学和遗传特征

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摘要

The application of molecular diagnostic techniques along with nucleotide sequence determination to permit contemporary phylogenetic analysis of European field isolates of equine infectious anemia virus (EIAV) has not been widely reported. As a result, of extensive testing instigated following the 2006 outbreak of equine infectious anemia in Italy, 24 farms with a history of exposure to this disease were included in this study. New PCR-based methods were developed, which, especially in the case of DNA preparations from peripheral blood cells, showed excellent correlation with OIE-approved agar gel immunodiffusion (AGID) tests for identifying EIAV-infected animals. In contrast, the OIE-recommended oligonucleotide primers for EIAV failed to react with any of the Italian isolates. Similar results were also obtained with samples from four Romanian farms. In addition, for the first time complete characterization of gag genes from five Italian isolates and one Romanian isolate has been achieved, along with acquisition of extensive sequence information (86% of the total gag gene) from four additional EIAV isolates (one Italian and three Romanian). Furthermore, in another 23 cases we accomplished partial characterization of gag gene sequences in the region encoding the viral matrix protein. Analysis of this information suggested that most Italian isolates were geographically restricted, somewhat reminiscent of the “clades” described for human immunodeficiency virus type 1 (HIV-1). Collectively this represents the most comprehensive genetic study of European EIAV isolates conducted to date.
机译:尚未广泛报道分子诊断技术与核苷酸序列确定技术的应用,以对欧洲马传染性贫血病毒的田间分离株进行当代的系统进化分析。结果,在2006年意大利爆发马传染性贫血之后,进行了广泛的测试,该研究包括24个有此病史的农场。已开发出基于PCR的新方法,特别是在从外周血细胞中提取DNA的情况下,该方法与OIE批准的琼脂凝胶免疫扩散(AGID)试验(用于识别EIAV感染的动物)表现出极好的相关性。相反,OIE推荐的EIAV寡核苷酸引物不能与任何意大利分离株反应。从四个罗马尼亚农场的样本中也获得了类似的结果。此外,首次获得了对来自五个意大利分离株和一个罗马尼亚分离株的 gag 基因的完整表征,并获得了广泛的序列信息(占总 gag的86%基因)来自另外四个EIAV分离株(一个意大利人和三个罗马尼亚人)。此外,在另外23个案例中,我们在编码病毒基质蛋白的区域中完成了 gag 基因序列的部分表征。对这些信息的分析表明,大多数意大利分离株在地理上受到限制,有点让人联想到针对1型人类免疫缺陷病毒(HIV-1)的“进化枝”。总的来说,这代表了迄今为止对欧洲EIAV分离株进行的最全面的遗传研究。

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