Foreign Animal Disease Research Unit, USDA/ARS Plum Island Animal Disease Center, PO Box 848, Greenport, NY 11944, USA.
Vet Pathol. 2010 Nov;47(6):1048-63. doi: 10.1177/0300985810372509. Epub 2010 Jun 29.
To characterize the early events of foot-and-mouth disease virus (FMDV) infection in cattle subsequent to simulated natural exposure, 16 steers were aerosol inoculated with FMDV and euthanized at various times. Samples were collected from each steer antemortem (serum, nasal swabs, and oral swabs) and postmortem (up to 40 tissues per animal) and screened for FMDV by virus isolation and for FMDV RNA by real-time reverse transcription polymerase chain reaction. Tissues that tested positive for FMDV or viral RNA were examined by immunohistochemistry and multichannel immunofluorescence microscopy. In previremic steers, FMDV was most consistently localized to nasopharyngeal tissues, thereby indicating this region as the most important site of primary viral replication. The earliest site of microscopic localization of FMDV antigens was the lymphoid follicle-associated epithelium of the pharyngeal mucosa-associated lymphoid tissue of the nasopharynx at 6 hours postaerosolization. At early time points after aerosol inoculation, viral antigens colocalized with cytokeratin-positive pharyngeal epithelial cells; intraepithelial FMDV-negative, MHCII/CD11c-double-positive dendritic cells were present in close proximity to FMDV-positive cells. Onset of viremia coincided with marked increase of viral loads in pulmonary tissues and with substantial decrease of viral detection in nasopharyngeal tissues. These data indicate that subsequent to aerogenous exposure to FMDV, the temporally defined critical pathogenesis events involve (1) primary replication in epithelial cells of the pharyngeal mucosa-associated lymphoid tissue crypts and (2) subsequent widespread replication in pneumocytes in the lungs, which coincides with (3) the establishment of sustained viremia.
为了描述牛口蹄疫病毒(FMDV)感染的早期事件,在模拟自然暴露后,16 头公牛通过气溶胶接种 FMDV 并在不同时间安乐死。在每个公牛生前(血清、鼻拭子和口腔拭子)和死后(每只动物多达 40 个组织)收集样本,并通过病毒分离和实时逆转录聚合酶链反应(PCR)筛选 FMDV RNA。对 FMDV 或病毒 RNA 检测呈阳性的组织通过免疫组织化学和多通道免疫荧光显微镜检查进行检查。在未出现病毒血症的牛中,FMDV 最常定位于鼻咽组织,从而表明该区域是原发性病毒复制的最重要部位。FMDV 抗原的最早微观定位部位是鼻咽喉黏膜相关淋巴组织的咽黏膜相关淋巴滤泡上皮,在气溶胶接种后 6 小时。在气溶胶接种后的早期时间点,病毒抗原与角蛋白阳性的咽上皮细胞共定位;在 FMDV 阳性细胞附近存在上皮内 FMDV 阴性、MHCII/CD11c 双阳性树突状细胞。病毒血症的发生与肺部组织中病毒载量的显著增加以及鼻咽组织中病毒检测的显著减少相吻合。这些数据表明,在气溶胶接触 FMDV 后,时间限定的关键发病机制事件包括(1)咽黏膜相关淋巴组织隐窝上皮细胞中的原发性复制和(2)随后在肺部的肺细胞中广泛复制,这与(3)持续病毒血症的建立相吻合。