Meehan J T, Cutlip R C, Lehmkuhl H D, Kluge J P, Ackermann M R
US Department of Agriculture, National Animal Disease Center, Ames, IA.
Vet Pathol. 1994 Mar;31(2):229-36. doi: 10.1177/030098589403100210.
Sixteen adult sheep (ten females, six males obtained from a closed flock at National Animal Disease Center, Ames, IA) were experimentally infected with bovine respiratory syncytial virus strain 375 (BRSV), and lung tissues were stained for viral antigen. Two infected sheep were euthanatized at each of the following post-inoculation times: 12, 24, 36, 48, 72, 96, 144, and 192 hours. Lung, nasal turbinates, trachea, right cranial bronchial and mediastinal lymph nodes, liver, and spleen were collected for histologic evaluation. An indirect immunoperoxidase technique was performed on routine paraffin-embedded sections of lung tissue, trachea, turbinates, and bronchial and mediastinal lymph nodes to determine the location of the BRSV antigen. For lung tissue from each sheep 400 light microscopic fields at 160x magnification were examined for staining for BRSV antigen. Lung tissue was also collected for virus and bacterial isolation. Daily serum samples were taken for determination of anti-BRSV titers. Severe respiratory disease was not produced in any sheep. Bovine respiratory syncytial virus was isolated from lung tissue collected from all sheep up through 144 hours post-inoculation. At 12 hours post-inoculation (case No. 2) respiratory syncytial virus antigen was detected in bronchiolar epithelium and a mononuclear cell within an alveolar space. Lung tissue from the sheep necropsied between 24 and 144 hours post-inoculation (case Nos. 3-14) contained BRSV antigen in bronchiolar epithelium, type I pneumocytes, type II pneumocytes, alveolar macrophages, and mononuclear cells within alveolar spaces. Macrophages staining for viral antigen were rare. Bronchiolar and type I epithelial cells comprised the majority of infected cells.(ABSTRACT TRUNCATED AT 250 WORDS)
16只成年绵羊(10只雌性,6只雄性,取自衣阿华州埃姆斯市国家动物疾病中心的一个封闭畜群)被实验性感染牛呼吸道合胞病毒375株(BRSV),并对肺组织进行病毒抗原染色。在接种后的以下各个时间点对2只感染的绵羊实施安乐死:12、24、36、48、72、96、144和192小时。收集肺、鼻甲、气管、右颅支气管和纵隔淋巴结、肝脏和脾脏进行组织学评估。对肺组织、气管、鼻甲以及支气管和纵隔淋巴结的常规石蜡包埋切片进行间接免疫过氧化物酶技术操作,以确定BRSV抗原的位置。对每只绵羊的肺组织,在160倍放大倍数下检查400个光学显微镜视野,以检测BRSV抗原染色情况。还收集肺组织用于病毒和细菌分离。每天采集血清样本以测定抗BRSV滴度。所有绵羊均未出现严重呼吸道疾病。在接种后144小时内,从所有绵羊收集的肺组织中均分离出牛呼吸道合胞病毒。在接种后12小时(病例2),在细支气管上皮和肺泡腔内的一个单核细胞中检测到呼吸道合胞病毒抗原。接种后24至144小时之间进行尸检的绵羊(病例3 - 14)的肺组织,在细支气管上皮、I型肺细胞、II型肺细胞、肺泡巨噬细胞以及肺泡腔内的单核细胞中含有BRSV抗原。染色显示病毒抗原的巨噬细胞很少见。细支气管和I型上皮细胞是受感染细胞的主要组成部分。(摘要截断于250字)