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首页> 外文期刊>Transboundary and emerging diseases >Sequence and phylogenetic analyses of the structural genes of virulent isolates and vaccine strains of Peste des petits ruminants virus from India.
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Sequence and phylogenetic analyses of the structural genes of virulent isolates and vaccine strains of Peste des petits ruminants virus from India.

机译:印度小反刍兽疫病毒的强毒分离株和疫苗株结构基因的序列和系统进化分析。

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摘要

Peste des petits ruminants (PPR) is an acute, highly contagious, notifiable and economically important transboundary viral disease of sheep and goats. In this study, sequence and phylogenetic analyses of structural protein genes, namely the nucleocapsid (N), the matrix (M), the fusion (F) and the haemagglutinin (H) coding sequences of virulent and vaccine strains of PPR virus (PPRV), were undertaken to determine the genetic variations between field isolates and vaccine strains. The open reading frame (ORF) of these genes of the isolates/strains was amplified by RT-PCR, cloned and sequenced. The ORF of N, M, F and H genes was 1578, 1008, 1641 and 1830 nucleotides (nt) in length and encodes polypeptides of 525, 335, 546 and 609 amino acids (aa), respectively, as reported earlier. Comparative sequence analyses of these four genes of isolates/strains were carried out with published sequences. It revealed an identity of 97.7-100% and 97.7-99.8% among the Asian lineage IV and 89.6-98.7% and 89.8-98.9% with other lineages of PPRV at nt and aa levels, respectively. The phylogenetic analyses of these isolates based on the aa sequences showed that all the viruses belonged to lineage IV along with other Asian isolates. This is in agreement with earlier observations that only PPRV lineage IV is in circulation in India since the disease was first reported. Further, sequence analysis of the thermostable/thermo-adapted vaccine strains showed no significant changes in the functional or structural surface protein-coding gene sequences. It is important to monitor the circulation of the PPRV in susceptible animals by H gene-based sequence comparisons in addition to the F gene- and N gene-based approaches to identify the distribution and spread of virus in the regular outbreaks that occur in endemic countries like India.
机译:小反刍兽疫(PPR)是一种急性,高度传染性,应通报且在经济上重要的绵羊和山羊跨界病毒病。在这项研究中,对结构蛋白基因的序列和系统发育分析,即PPR病毒(PPRV)强毒株和疫苗株的核衣壳(N),基质(M),融合蛋白(F)和血凝素(H)编码序列进行,以确定田间分离株和疫苗株之间的遗传变异。通过RT-PCR扩增分离物/菌株的这些基因的开放阅读框(ORF),进行克隆和测序。 N,M,F和H基因的ORF长度分别为1578、1008、1641和1830个核苷酸(nt),分别编码525、335、546和609个氨基酸(aa)的多肽。用公开的序列对分离株/菌株的这四个基因进行比较序列分析。它揭示了亚洲谱系IV中的97.7-100%和97.7-99.8%的同一性,在nt和aa水平上与其他PPRV谱系的同一性分别为89.7-98.7%和89.8-98.9%。根据aa序列对这些分离株的系统发育分析表明,所有病毒与其他亚洲分离株均属于IV谱系。这与较早的观察结果一致,因为自该病首次报道以来,仅PPRV血统IV在印度流通。此外,对热稳定/热适应的疫苗株的序列分析表明,功能或结构表面蛋白编码基因序列没有明显变化。除了基于F基因和N基因的方法之外,还必须通过基于H基因的序列比较来监测易感动物中PPRV的循环,以鉴定在流行国家发生的常规暴发中病毒的分布和传播像印度。

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