Foreign Animal Disease Research Unit, USDA-ARS, Plum Island Animal Disease Center, Greenport, New York, USA
Department of Veterinary Population Medicine, University of Minnesota, St. Paul, Minnesota, USA.
mSphere. 2018 Dec 12;3(6):e00493-18. doi: 10.1128/mSphere.00493-18.
The pathogenesis of foot-and-mouth disease virus (FMDV) in cattle was investigated through early and late stages of infection by use of an optimized experimental model for controlled contact exposure. Time-limited exposure of cattle to FMDV-infected pigs led to primary FMDV infection of the nasopharyngeal mucosa in both vaccinated and nonvaccinated cattle. In nonvaccinated cattle, the infection generalized rapidly to cause clinical disease, without apparent virus amplification in the lungs prior to establishment of viremia. Vaccinated cattle were protected against clinical disease and viremia; however, all vaccinated cattle were subclinically infected, and persistent infection occurred at similarly high prevalences in both animal cohorts. Infection dynamics in cattle were consistent and synchronous and comparable to those of simulated natural and needle inoculation systems. However, the current experimental model utilizes a natural route of virus exposure and is therefore superior for investigations of disease pathogenesis and host response. Deep sequencing of viruses obtained during early infection of pigs and cattle indicated that virus populations sampled from sites of primary infection were markedly more diverse than viruses from vesicular lesions of cattle, suggesting the occurrence of substantial bottlenecks associated with vesicle formation. These data expand previous knowledge of FMDV pathogenesis in cattle and provide novel insights for validation of inoculation models of bovine FMD studies. Foot-and-mouth disease virus (FMDV) is an important livestock pathogen that is often described as the greatest constraint to global trade in animal products. The present study utilized a standardized pig-to-cow contact exposure model to demonstrate that FMDV infection of cattle initiates in the nasopharyngeal mucosa following natural virus exposure. Furthermore, this work confirmed the role of the bovine nasopharyngeal mucosa as the site of persistent FMDV infection in vaccinated and nonvaccinated cattle. The critical output of this study validates previous studies that have used simulated natural inoculation models to characterize FMDV pathogenesis in cattle and emphasizes the importance of continued research of the unique virus-host interactions that occur within the bovine nasopharynx. Specifically, vaccines and biotherapeutic countermeasures designed to prevent nasopharyngeal infection of vaccinated animals could contribute to substantially improved control of FMDV.
口蹄疫病毒(FMDV)在牛中的发病机制通过使用经优化的用于受控接触暴露的实验模型在感染的早期和晚期进行了研究。对牛进行限时接触感染 FMDV 的猪,导致接种和未接种疫苗的牛的鼻咽黏膜原发性 FMDV 感染。在未接种疫苗的牛中,感染迅速扩散导致临床疾病,在建立血症之前肺部没有明显的病毒扩增。接种疫苗的牛受到保护免受临床疾病和血症的侵害;然而,所有接种疫苗的牛均亚临床感染,并且在两个动物群中持续性感染的发生率相似。牛的感染动力学是一致的和同步的,与模拟自然和针刺接种系统相当。然而,目前的实验模型利用病毒暴露的自然途径,因此更适合于疾病发病机制和宿主反应的研究。对猪和牛早期感染时获得的病毒进行深度测序表明,从原发性感染部位采样的病毒群体明显比牛水疱病变中的病毒多样化,表明与水疱形成相关的大量瓶颈的发生。这些数据扩展了牛口蹄疫发病机制的先前知识,并为牛口蹄疫接种模型的验证提供了新的见解。口蹄疫病毒(FMDV)是一种重要的家畜病原体,通常被描述为动物产品全球贸易的最大限制因素。本研究利用标准化的猪-牛接触暴露模型证明,牛的 FMDV 感染在自然病毒暴露后从鼻咽黏膜开始。此外,这项工作证实了牛的鼻咽黏膜是接种疫苗和未接种疫苗的牛中持续性 FMDV 感染的部位。这项研究的关键结果验证了以前使用模拟自然接种模型来描述牛中 FMDV 发病机制的研究,并强调了对在牛的鼻咽部发生的独特病毒-宿主相互作用进行持续研究的重要性。具体而言,旨在预防接种动物鼻咽部感染的疫苗和生物治疗对策可以为 FMDV 的有效控制做出重大贡献。