Centre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark; Present address: Weinberger Lab, Laboratory of Epidemiology and Public Health, Yale School of Medicine, 60 College Street, 06510 New Haven, CT and
Centre for GeoGenetics, Natural History Museum of Denmark, Soelvgade 83 S, Copenhagen K, DK-1307, Denmark; Stanford University, School of Medicine, 300 Pasteur Drive, CA 94305, USA.
Evol Med Public Health. 2015 Oct 27;2015(1):289-303. doi: 10.1093/emph/eov026.
Swine vesicular disease virus (SVDV) is a close relative of the human Enterovirus B serotype, coxsackievirus B5. As the etiological agent of a significant emergent veterinary disease, several studies have attempted to explain its origin. However, several key questions remain, including the full biological ancestry of the virus, and its geographical and temporal origin.
We sequenced near-complete genomes of 27 SVDV and 13 coxsackievirus B5 samples, all originally isolated between 1966 and 2006, and analysed these in conjunction with existing sequences and historical information.
While analyses incorporating 24 additional near-complete SVDV genomic sequences indicate clear signs of within-SVDV recombination, all 51 SVDV isolates remain monophyletic. This supports a hypothesis of a single anthroponotic transfer origin. Analysis of individual coding and non-coding regions supports that SVDV has a recombinant origin between coxsackievirus B5 and another Enterovirus B serotype, most likely coxsackievirus A9. Extensive Bayesian sequence-based analysis of the time of the most recent common ancestor of all analysed sequences places this within a few years around 1961. Epidemiological evidence points to China as an origin, but there are no available samples to test this conclusively.
Historical investigation and the clinical aspects of the involved Enterovirus B serotypes, makes the current results consistent with a hypothesis stating that SVDV originated through co-infection, recombination, and a single anthroponotic event, during large viral meningitis epidemics around 1960/1961 involving the ancestral serotypes. The exact geographical origin of SVDV may remain untestable due to historical aspects.
猪水疱病病毒(SVDV)是与人类肠道病毒 B 型柯萨奇病毒 B5 密切相关的病毒。作为一种重要的新兴兽医疾病的病原体,已有多项研究试图解释其起源。然而,仍有几个关键问题尚未解决,包括病毒的完整生物学起源及其地理和时间起源。
我们对 27 株 SVDV 和 13 株柯萨奇病毒 B5 样本的近全长基因组进行了测序,这些样本均于 1966 年至 2006 年间首次分离,我们结合现有序列和历史信息对这些样本进行了分析。
虽然纳入 24 个额外的近全长 SVDV 基因组序列的分析表明存在明显的 SVDV 内重组迹象,但所有 51 株 SVDV 分离株仍然是单系的。这支持了一个单一的人兽共患病转移起源的假说。对单个编码和非编码区域的分析支持 SVDV 起源于柯萨奇病毒 B5 和另一种肠道病毒 B 型血清型之间的重组,最有可能是柯萨奇病毒 A9。对所有分析序列最近共同祖先时间的广泛贝叶斯序列分析将其置于 1961 年前后的几年内。流行病学证据指向中国作为起源地,但目前尚无可用样本进行明确验证。
历史调查和涉及的肠道病毒 B 型血清型的临床特征,使目前的结果与一个假说一致,即 SVDV 是通过在 1960/1961 年期间涉及祖先血清型的大规模病毒性脑膜炎流行期间的合并感染、重组和单一人兽共患病事件而产生的。由于历史方面的原因,SVDV 的确切地理起源可能仍无法验证。