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Vp5 Gene Based Molecular Characterization of Bluetongue Virus 9 from South India

机译:来自南部印度的蓝舌病毒9基于Vp5基因的分子表征

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Bluetongue virus (BTV) is a prototype species of the genus Orbivirus within the family Reoviridae that causes Bluetongue disease (BT) in domestic as well as wild ruminants. The BTV isolate Ong5/06/Ind was isolated from sheep in Andhra Pradesh state in 2006. The isolate was confirmed as BTV based on characteristics CPE in BHK21 cell culture, 3:3:3:1 migration pattern of viral nucleic acid in RNA–PAGE and 366bp amplicon with group specific ns1 gene based PCR. VP5 gene based serotype specific primer produced specific PCR amplicon of 823bp corresponding to BTV serotype 9. Nucleotide sequence analysis revealed 97% identity with other Indian and European BTV–9 isolates, more than 90% with Asian and, only 68.8% with South African isolates. However, based on deduced amino acids, the identity was more than 97% with Indian, Asian and European and, only 73.4% with South African BTV–9 isolates. The in–silico restriction enzyme analysis (REA) with AflIII, BtrI and HindII showed a common pattern of restriction sites in Indian and European isolates at 1152, 1153 and 591, respectively. The lack of any of these restriction sites in African and other Asian isolates revealed the European origin of the study isolate. Similarly, the lack of BsmAI restriction site in Ong5/06/Ind isolate (Accession no. JF969307), differentiate it from European, Asian and South Africa isolates. The sequence analysis revealed that Ong5/06/Ind, Asian and European BTV–9 isolates were placed in nucleotype ‘C’ while South African isolates were placed in nucleotype ‘B’.
机译:蓝舌病病毒(BTV)是呼肠孤病毒科中Orbivirus的原型物种,可在家庭以及野生反刍动物中引起蓝舌病(BT)。 BTV分离株Ong5 / 06 / Ind于2006年从安得拉邦的绵羊中分离出来。根据BHK21细胞培养中CPE的特征,RNA中病毒核酸的3:3:3:1迁移模式,该分离株被确认为BTV。 PAGE和366bp扩增子以及基于组特异性ns1基因的PCR。基于VP5基因的血清型特异性引物产生了823bp的特异性PCR扩增子,对应于BTV血清型9。核苷酸序列分析显示,与其他印度和欧洲BTV-9分离株的同源性为97%,与亚洲分离株的分离率为90%以上,与南非分离株的分离率为68.8%。 。但是,根据推导的氨基酸,印度,亚洲和欧洲的身份认同率超过97%,而南非BTV-9分离株的认同率仅为73.4%。使用AflIII,BtrI和HindII进行的计算机限制性内切酶分析(REA)显示,印度和欧洲分离株中分别位于1152、1153和591处的限制性酶切位点常见模式。在非洲和其他亚洲分离株中没有任何这些限制位点,这表明该研究分离株的欧洲起源。同样,在Ong5 / 06 / Ind分离株(保藏号JF969307)中缺乏BsmAI限制性酶切位点,将其与欧洲,亚洲和南非分离株区分开。序列分析显示,Ong5 / 06 / Ind,亚洲和欧洲的BTV–9分离株被置于C型,而南非分离株被置于B型。

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