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首页> 外文期刊>Archives of Virology >Isolation of bluetongue virus serotype 1 (BTV-1) from goats and its phylogenetic relationship to other BTV-1 isolates worldwide based on full-length sequence of genome segment-2
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Isolation of bluetongue virus serotype 1 (BTV-1) from goats and its phylogenetic relationship to other BTV-1 isolates worldwide based on full-length sequence of genome segment-2

机译:从山羊分离出蓝舌病毒血清型1(BTV-1)及其与全球其他BTV-1分离株的系统发生关系,基于基因组segment-2的全长序列

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Eight bluetongue viruses (BTV) were isolated in BHK-21 cell culture from blood of goats suffering from peste des petits ruminants. These viruses were identified as BTV serotype 1 (BTV-1) by RT-PCR using VP2-gene-based primers coupled with sequencing of the PCR products. All of the isolates showed similar genome migration profile in 8% polyacrylamide gel electrophoresis. The genome segment-2 (seg-2) of one isolate (MKD18/India/2008) was amplified piecemeal by overlapping PCR, and the products were sequenced to obtain full-length seg-2. Phylogenetic analysis based on the seg-2 sequence revealed that MKD18 is closely related to Australian BTV-1 isolates, with 86.3–86.8% nucleotide identity. Phylogenetic analysis based on the partial sequence of seg-2 (541 bp, nucleotides 1,304–1,844) showed that the Indian BTV-1 isolates, namely, MKD18, Avikanagar, Sirsa-3 and Chennai, are very closely related to each other, with more than 99.6% nucleotide identity. Although a high degree of similarity exists, the Indian BTV-1 isolates collected over the past 25 years should be studied to demonstrate the co-existence of different VP2 antigenic profiles.
机译:在BHK-21细胞培养物中,从患有小反刍动物的山羊血液中分离出八种蓝舌病毒(BTV)。使用基于VP2基因的引物和PCR产物测序,通过RT-PCR将这些病毒鉴定为BTV血清型1(BTV-1)。所有分离物在8%聚丙烯酰胺凝胶电泳中均显示出相似的基因组迁移谱。通过重叠PCR逐片扩增一种分离株(MKD18 / India / 2008)的基因组segment-2(seg-2),并对产物进行测序以获得全长seg-2。基于seg-2序列的系统发育分析表明,MKD18与澳大利亚BTV-1分离株密切相关,具有86.3–86.8%的核苷酸同一性。基于seg-2的部分序列(541 bp,核苷酸1,304–1,844)的系统发育分析表明,印度BTV-1分离株,即MKD18,Avikanagar,Sirsa-3和Chennai,彼此之间密切相关,与核苷酸同一性超过99.6%。尽管存在高度相似性,但应该研究过去25年中收集的印度BTV-1分离株,以证明不同VP2抗原谱的共存。

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