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喀麦隆非洲猪瘟病毒分离株的全基因组序列分析。

Full genome sequence analysis of African swine fever virus isolates from Cameroon.

机构信息

The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey, United Kingdom.

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald, Insel Riems, Germany.

出版信息

PLoS One. 2024 Mar 21;19(3):e0293049. doi: 10.1371/journal.pone.0293049. eCollection 2024.

Abstract

African swine fever (ASF) is a devastating disease of domestic pigs that has spread across the globe since its introduction into Georgia in 2007. The etiological agent is a large double-stranded DNA virus with a genome of 170 to 180 kb in length depending on the isolate. Much of the differences in genome length between isolates are due to variations in the copy number of five different multigene families that are encoded in repetitive regions that are towards the termini of the covalently closed ends of the genome. Molecular epidemiology of African swine fever virus (ASFV) is primarily based on Sanger sequencing of a few conserved and variable regions, but due to the stability of the dsDNA genome changes in the variable regions occur relatively slowly. Observations in Europe and Asia have shown that changes in other genetic loci can occur and that this could be useful in molecular tracking. ASFV has been circulating in Western Africa for at least forty years. It is therefore reasonable to assume that changes may have accumulated in regions of the genome other than the standard targets over the years. At present only one full genome sequence is available for an isolate from Western Africa, that of a highly virulent isolate collected from Benin during an outbreak in 1997. In Cameroon, ASFV was first reported in 1981 and outbreaks have been reported to the present day and is considered endemic. Here we report three full genome sequences from Cameroon isolates of 1982, 1994 and 2018 outbreaks and identify novel single nucleotide polymorphisms and insertion-deletions that may prove useful for molecular epidemiology studies in Western Africa and beyond.

摘要

非洲猪瘟(ASF)是一种毁灭性的家猪疾病,自 2007 年传入格鲁吉亚以来,已在全球范围内传播。病原体是一种长度为 170 到 180 kb 的大型双链 DNA 病毒,其基因组长度取决于分离株。分离株之间基因组长度的大部分差异是由于编码在基因组共价封闭末端末端重复区域的五个不同多基因家族的拷贝数变化引起的。非洲猪瘟病毒(ASFV)的分子流行病学主要基于几个保守和可变区域的 Sanger 测序,但由于 dsDNA 基因组的稳定性,可变区域的变化相对较慢。欧洲和亚洲的观察结果表明,其他遗传位点的变化可能会发生,这在分子追踪中可能很有用。ASFV 在西非已经流行了至少四十年。因此,可以合理地假设,多年来,除了标准靶标之外,基因组的其他区域可能已经积累了变化。目前,仅在西非的一个分离株中提供了一个完整的基因组序列,该序列是 1997 年在贝宁爆发期间从一个高毒力分离株中收集的。在喀麦隆,ASF 于 1981 年首次报告,至今仍有暴发报告,并被认为是地方性的。在这里,我们报告了来自喀麦隆 1982 年、1994 年和 2018 年暴发的三个完整的基因组序列,并确定了可能对西非及其他地区的分子流行病学研究有用的新的单核苷酸多态性和插入缺失。

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