Blackmore C G, Grimstad P R
Department of Biological Sciences, University of Notre Dame, Indiana, USA.
Am J Trop Med Hyg. 1998 Nov;59(5):704-9. doi: 10.4269/ajtmh.1998.59.704.
Cache Valley virus (CVV) and Potosi virus (POTV) are two closely related mosquito-borne viruses (Bunyaviridae: Bunyamwera group) that appear to circulate in several regions of the United States, especially the Midwest. We determined the prevalence of specific neutralizing antibodies to both viruses in Indiana white-tailed deer and conducted infection experiments to assess whether deer could serve as an vertebrate-amplifying host. Cross-infection experiments also were carried out to investigate the level of antibody cross-reactivity and cross-protection between the two viruses. The seroprevalence rate was high for both CVV (> 66%) and POTV (> 43%) in adult deer statewide. Antibodies neutralizing CVV were more common among deer harvested in the northern part of Indiana whereas the prevalence of POTV antibodies suggested a more southern distribution for this virus. Experimental infections of captive deer showed that they may serve as amplifying hosts for either virus. Deer infected with CVV or POTV developed a 1-3-day viremia with 3.0 and 4.1 log10 plaque-forming units/ml mean peak titers, respectively. However, significant levels of antibody cross-reactivity between the two viruses were observed. Viremia was lower and shorter when animals immune to either CVV or POTV were cross-infected with the alternate virus and antibody responses following cross-infections resembled original antigenic sin with higher titers of antibodies against the primary agent.
卡奇谷病毒(CVV)和波托西病毒(POTV)是两种密切相关的蚊媒病毒(布尼亚病毒科:布尼亚姆韦拉病毒群),似乎在美国的几个地区传播,尤其是中西部地区。我们测定了印第安纳州白尾鹿体内针对这两种病毒的特异性中和抗体的流行率,并进行了感染实验,以评估鹿是否可作为脊椎动物扩增宿主。还开展了交叉感染实验,以研究两种病毒之间的抗体交叉反应水平和交叉保护情况。全州成年鹿中,CVV(>66%)和POTV(>43%)的血清阳性率都很高。中和CVV的抗体在印第安纳州北部捕获的鹿中更为常见,而POTV抗体的流行率表明该病毒在更偏南的地区分布。圈养鹿的实验性感染表明,它们可能作为这两种病毒的扩增宿主。感染CVV或POTV的鹿出现了1 - 3天的病毒血症,平均峰值滴度分别为3.0和4.1 log10蚀斑形成单位/毫升。然而,观察到两种病毒之间存在显著水平的抗体交叉反应。当对CVV或POTV免疫的动物被另一种病毒交叉感染时,病毒血症更低且持续时间更短,交叉感染后的抗体反应类似于原始抗原罪,针对主要病原体的抗体滴度更高。