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Experimental Infection of Calves by Two Genetically-Distinct Strains of Rift Valley Fever Virus

机译:裂谷热病毒的两个遗传不同菌株对小牛的实验感染

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摘要

Recent outbreaks of Rift Valley fever in ruminant livestock, characterized by mass abortion and high mortality rates in neonates, have raised international interest in improving vaccine control strategies. Previously, we developed a reliable challenge model for sheep that improves the evaluation of existing and novel vaccines in sheep. This sheep model demonstrated differences in the pathogenesis of Rift Valley fever virus (RVFV) infection between two genetically-distinct wild-type strains of the virus, Saudi Arabia 2001 (SA01) and Kenya 2006 (Ken06). Here, we evaluated the pathogenicity of these two RVFV strains in mixed breed beef calves. There was a transient increase in rectal temperatures with both virus strains, but this clinical sign was less consistent than previously reported with sheep. Three of the five Ken06-infected animals had an early-onset viremia, one day post-infection (dpi), with viremia lasting at least three days. The same number of SA01-infected animals developed viremia at 2 dpi, but it only persisted through 3 dpi in one animal. The average virus titer for the SA01-infected calves was 1.6 logs less than for the Ken06-infected calves. Calves, inoculated with either strain, seroconverted by 5 dpi and showed time-dependent increases in their virus-neutralizing antibody titers. Consistent with the results obtained in the previous sheep study, elevated liver enzyme levels, more severe liver pathology and higher virus titers occurred with the Ken06 strain as compared to the SA01 strain. These results demonstrate the establishment of a virulent challenge model for vaccine evaluation in calves.
机译:反刍动物最近爆发裂谷热,以大规模流产和新生儿高死亡率为特征,引起了国际社会对改进疫苗控制策略的兴趣。以前,我们为绵羊开发了一种可靠的挑战模型,可以改善对绵羊中现有和新型疫苗的评估。该绵羊模型证明了裂谷热病毒(RVFV)感染在两种遗传上不同的野生型病毒之间的差异,沙特阿拉伯2001(SA01)和肯尼亚2006(Ken06)。在这里,我们评估了这两种RVFV菌株在混合品种牛犊中的致病性。两种病毒株的直肠温度都有短暂的升高,但是这种临床体征与先前报道的绵羊相比并不一致。在感染Ken06的五只动物中,有三只在感染后一天(dpi)出现了早期病毒血症,病毒血症持续至少三天。相同数量的SA01感染动物在2 dpi时出现病毒血症,但在一只动物中仅持续3 dpi。 SA01感染牛犊的平均病毒滴度比Ken06感染牛犊的平均病毒滴度少1.6 log。接种任何一种菌株的小牛,其血清均转化为5 dpi,并显示其病毒中和抗体效价随时间的增加。与先前的绵羊研究获得的结果一致,与SA01菌株相比,Ken06菌株的肝脏酶水平升高,肝脏病理更为严重,病毒滴度更高。这些结果证明了针对牛犊中疫苗评估的有力挑战模型的建立。

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