哈萨克斯坦野生鸟类禽原avulavirus 1(新城疫病病毒基因型VIg或新基因型XXI.)全基因组分析

V. Strochkov, Y. Burashev, S. Nurlan, ybayev, G. Xie, T. Erkkila, H. Cui, J. Fair
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引用次数: 2

摘要

背景:新城疫病毒(NDV)具有显著的多样性和流动性,其中包括基因型VI的强毒病毒。这些病毒通常被称为鸽子副粘病毒1,因为它们通常被分离出来,并在鸽科鸟类中引起临床疾病。基因型VI病毒偶尔感染,也可能引起家禽临床疾病。因此,新城疫的演变、传播现状和发现与禽类健康息息相关。方法:对3株哈萨克斯坦分离株进行核苷酸测序和系统发育研究,以确定融合(F)蛋白的完整基因和全基因组序列。序列数据比较了代表不同NDV基因型和亚基因型的106个融合基因,以及225个融合基因和37个来自世界不同地区、不同时期的VI类NDV菌株的全基因组。构建了系统发育树来确定这些菌株之间的进化关系。我们分析了融合蛋白基因和全基因组序列,包括裂解位点。结果:3株分离物全基因组长度分别为15142bp、15085bp和15102bp,与新城疫病毒VIg基因型相似,基因序列为3′-NP-P-M-F-HN-L-5′。融合蛋白的裂解位点为112KRQKR116-F117,这一特征通常与致命的NDV菌株有关。基于基因组序列、SNP和融合基因序列的系统发育分析表明,3株分离株可归类为II类基因型VIg NDVs。系统发育分析表明,来自哈萨克斯坦不同地点的新城疫具有高度的遗传相似性,并与VIg基因型新城疫聚集在一起。根据我们的数据分析,VIg分离株与VIg亚基因型的俄罗斯和乌克兰分离株具有最高的序列一致性,表明该地区可能通过跨境活禽贸易传播了速度性NDV。结论:我们的研究提供了在哈萨克斯坦流行的新城疫病毒遗传特征的基线信息,我们建议对毒力新城疫的进化和流行病学研究可以帮助提供在该地区流行的变异的准确分子数据,从而帮助设计更有效的重组疫苗。
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Whole Genomes of Avian orthoavulavirus 1 (Newcastle Disease Virus Genotypes VIg or new genotype XXI.) in Wild Birds in Kazakhstan
Background: The remarkable diversity and mobility of Newcastle disease viruses (NDV) includes virulent viruses of genotype VI. These viruses are often referred to as pigeon paramyxoviruses 1 because they are normally isolated and cause clinical disease in birds from the Columbidae family. Genotype VI viruses occasionally infect, and may also cause clinical disease in poultry. Thus, the evolution, current spread and detection of NDV are relevant to avian health. Methods: Nucleotide sequencing and phylogenetic studies of three Kazakhstan isolations were performed to characterize the complete fusion (F)-protein gene as well as whole genome sequence. Sequence data were compared with 106 Fusion genes representing different NDV genotypes and sub-genotypes, as well as 225 fusion genes and 37 whole genome of class VI NDV strains from different regions of the world at different time periods. Phylogenetic trees were constructed to determine evolutionary relationships among these strains. We analysed fusion (F) protein gene and whole genome sequences, including the cleavage site. Results: The complete genome of these 3 isolates contained 15142bp, 15085bp and 15102bp in length, similar to those of Newcastle disease virus (NDV) strains in genotypes VIg, with the gene order 3’-NP-P-M-F-HN-L-5’. The cleavage site of the fusion protein was 112KRQKR116-F117, a feature generally associated with virulent NDV strains. Phylogenetic analysis, based on genomic sequences, SNP and fusion gene sequences, revealed that three isolates should be classified as class II genotype VIg NDVs. Phylogenetic analysis revealed that the NDV from various sites in Kazakhstan was highly similar genetically and that it clustered together with NDV of genotype VIg. Based on our data analysis, VIg isolates shared highest sequence identity with Russian and Ukraine isolates of the VIg subgenotype, suggests the possible spread of velogenic NDV in this region through cross-border live bird trade. Conclusion: Our study provides baseline information on the genetic characteristics of NDV circulating in Kazakhstan and we propose that the evolutionary and epidemiological study of virulent NDV could help to provide accurate molecular data about variants circulating in this region, thus aiding in the design of more efficient recombinant vaccines.
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