未经病毒序列富集的九个非洲猪瘟病毒 (ASFV) 东非 p72 基因型 IX 病毒分离株的完整基因组测序和比较系统发生组学研究

Viruses Pub Date : 2024-09-14 DOI:10.3390/v16091466
Jean-Baka Domelevo Entfellner, Edward Abworo Okoth, Cynthia Kavulani Onzere, Chris Upton, Emma Peter Njau, Dirk Höper, Sonal P. Henson, Samuel O. Oyola, Edwina Bochere, Eunice M. Machuka, Richard P. Bishop
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摘要

非洲猪瘟病毒(ASFV)是非洲野猪(Phacochoerus 和 Potamochoerus)和软蜱(Ornithodoros soft ticks)的地方性传染病。然而,ASFV 会导致欧亚家猪(Sus scrofa)患上致命疾病。虽然撒哈拉以南非洲地区被认为是 ASFV 的原产地,但公开的 ASFV 全基因组序列显示,p72 基因型 I 和 II 有很强的偏向性,而这两种基因型是非洲以外地区家猪大流行的罪魁祸首。为了减少这种偏差,我们在此描述了 p72 基因型 IX 中的九个新的东非完整基因组,并将所有 16 个可用的基因型 IX 基因组与其他 ASFV p72 支系进行了系统发育分析。我们还记录了一个特定的新基因型 IX 基因组序列(KE/2013/Busia.3)与野猪细胞传代衍生物在基因组水平上的差异。基因型 IX 基因组与现有的五个基因型 X 基因组聚集在一起。相比之下,基因型 IX 和 X 基因组在系统发育上与所有其他 ASFV 基因组有很大区别。基于 p72 的病毒检测引物所基于的 p72 基因区在基因九型中含有一致的 SNP,可能导致检测灵敏度降低。除上述细胞适应变体外,还测定了 8 个新型 ASFV 基因型 IX 基因组:5 个来自在原代猪外周血单核细胞中传代一次的病毒,3 个来自直接从现场取样的肾组织中分离的 DNA。基于这种方法学上的简化,ASFV 现场分离物的基因组测序应该会越来越常规化,从而在全基因组水平上迅速扩展有关非洲 ASFV 多样性的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complete Genome Sequencing and Comparative Phylogenomics of Nine African Swine Fever Virus (ASFV) Isolates of the Virulent East African p72 Genotype IX without Viral Sequence Enrichment
African swine fever virus (ASFV) is endemic to African wild pigs (Phacochoerus and Potamochoerus), in which viral infection is asymptomatic, and Ornithodoros soft ticks. However, ASFV causes a lethal disease in Eurasian domestic pigs (Sus scrofa). While Sub-Saharan Africa is believed to be the original home of ASFV, publicly available whole-genome ASFV sequences show a strong bias towards p72 Genotypes I and II, which are responsible for domestic pig pandemics outside Africa. To reduce this bias, we hereby describe nine novel East African complete genomes in p72 Genotype IX and present the phylogenetic analysis of all 16 available Genotype IX genomes compared with other ASFV p72 clades. We also document genome-level differences between one specific novel Genotype IX genome sequence (KE/2013/Busia.3) and a wild boar cell-passaged derivative. The Genotype IX genomes clustered with the five available Genotype X genomes. By contrast, Genotype IX and X genomes were strongly phylogenetically differentiated from all other ASFV genomes. The p72 gene region, on which the p72-based virus detection primers are derived, contains consistent SNPs in Genotype IX, potentially resulting in reduced sensitivity of detection. In addition to the abovementioned cell-adapted variant, eight novel ASFV Genotype IX genomes were determined: five from viruses passaged once in primary porcine peripheral blood monocytes and three generated from DNA isolated directly from field-sampled kidney tissues. Based on this methodological simplification, genome sequencing of ASFV field isolates should become increasingly routine and result in a rapid expansion of knowledge pertaining to the diversity of African ASFV at the whole-genome level.
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