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A50 Whole-genome sequencing of African swine fever isolates from Sardinia

机译:A50撒丁岛非洲猪瘟分离株的全基因组测序

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摘要

In order to assess the molecular epidemiology of African swine fever (ASF) in Sardinia, we analyzed a wide range of isolates from wild and domestic pigs over a 31-year period (1978–2009) by genotyping sequence data from the genes encoding the p54 and the p72 proteins and the CVR. On this basis, the analysis of the B602L gene revealed a minor difference, placing the Sardinian isolates into two clusters according to their temporal distribution. As an extension of this study, in order to achieve a higher level of discrimination, three further variable genome regions, namely p30, CD2v, and I73R/I329L, of a large number of isolates collected from outbreaks in the years 2002–14 have been investigated. Sequence analysis of the CD2v region revealed a temporal subdivision of the viruses into two subgroups. These data, together with those from the B602L gene analysis, demonstrated that the viruses circulating in Sardinia belong to p72/genotype I, but since 1990 have undergone minor genetic variations in respect to its ancestor, thus making it impossible to trace isolates, enabling a more accurate assessment of the origin of outbreaks, and extending knowledge of virus evolution. To solve this problem, we have sequenced and annotated the complete genome of nine ASF isolates collected in Sardinia between 1978 and 2012. This was achieved using sequence data determined by next-generation sequencing. The results showed a very high identity with range of nucleotide similarity among isolates of 99.5 per cent to 99.9 per cent. The ASF virus (ASFV) genomes were composed of terminal inverted repeats and conserved and non-conserved ORFs. Among the conserved ORFs, B385R, H339R, and O61R-p12 showed 100 per cent amino acid identity. The same was true for the hypervariable ORFs, with regard to X69R, DP96R, DP60R, EP153R, B407L, I10L, and L60L genes. The EP402R and B602L genes showed, as expected, an amino acid identity range of 98.5 per cent to 100 per cent and 91 per cent to 100 per cent, respectively. In addition, all of the isolates displayed variable intergenic sequences. As a whole, the results from our studies confirmed a remarkable genetic stability of the ASFV/p72 genotype I viruses circulating in Sardinia.
机译:为了评估撒丁岛非洲猪瘟(ASF)的分子流行病学,我们通过对编码p54的基因进行了基因分型,对31年内(1978-2009)的野生和家猪分离株进行了分析以及p72蛋白和CVR。在此基础上,对B602L基因的分析显示出较小的差异,根据其时间分布将撒丁岛分离株分为两个簇。作为这项研究的延伸,为了实现更高的区分度,从2002–14年暴发中收集到的大量分离株中的三个另外的可变基因组区域,即p30,CD2v和I73R / I329L,已经被分离出来。调查。 CD2v区的序列分析显示病毒在时间上分为两个亚组。这些数据以及来自B602L基因分析的数据表明,撒丁岛中传播的病毒属于p72 / I型,但自1990年以来,其祖先经历了微小的遗传变异,因此无法追踪分离株,从而可以更准确地评估爆发的起源,并扩展病毒进化知识。为了解决这个问题,我们对1978年至2012年间在撒丁岛收集的9种ASF分离株的完整基因组进行了测序和注释。这是通过下一代测序确定的序列数据实现的。结果显示,分离株之间的核苷酸相似性范围的一致性非常高,为99.5%至99.9%。 ASF病毒(ASFV)基因组由末端反向重复序列以及保守的和非保守的ORF组成。在保守的ORF中,B385R,H339R和O61R-p12具有100%的氨基酸同一性。对于X69R,DP96R,DP60R,EP153R,B407L,I10L和L60L基因,高变ORF也是如此。正如预期的那样,EP402R和B602L基因的氨基酸同一性范围分别为98.5%至100%和91%至100%。此外,所有分离株均显示出可变的基因间序列。总体而言,我们的研究结果证实了撒丁岛流行的ASFV / p72基因型I病毒具有显着的遗传稳定性。

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