Shoup D I, Swayne D E, Jackwood D J, Saif L J
Department of Veterinary Preventive Medicine, Ohio Agricultural Research and Development Center, Ohio State University, Wooster 44691, USA.
J Vet Diagn Invest. 1996 Apr;8(2):161-7. doi: 10.1177/104063879600800204.
An immunohistochemistry technique was developed using fixed tissues to study the presence and location of transmissible gastroenteritis virus (TGEV) antigens in situ. Experimentally infected gnotobiotic and conventional pigs as well as pigs with natural TGEV infection were examined. The staining technique was based on detection of the major structural protein of TGEV, the nucleocapsid, by using a pool of 3 monoclonal antibodies. Formalin and periodate-lysine-paraformaldehyde (PLP)-fixed intestinal tissues from a gnotobiotic pig inoculated with virulent TGEV were used to determine optimal antibody concentrations and incubation times. The intestinal tissues remained in their respective fixatives for 6 months, and serial sections were removed at sequential times and embedded in paraffin blocks. PLP and 10% neutral buffered formalin were acceptable fixatives and preserved TGEV nucleocapsid antigenicity for up to 6 months. Formalin, in comparison with PLP as a fixative, was better for preserving original tissue morphology and provided better antigen detection. Conventional crossbred pigs were inoculated with virulent TGEV, and animals were euthanized on various postexposure days. Intestinal tissues were positive for TGEV nucleocapsid antigens on postexposure days 2, 4, and 8. The immunohistochemistry technique detected TGEV antigen in stored paraffin-embedded tissues from 14 naturally infected pigs previously confirmed as positive for TGEV using a direct immunofluorescence assay on intestinal mucosal smears, whereas 9 naturally infected pigs confirmed negative for TGEV antigen by the same immunofluorescence assay showed no staining consistent with the presence of TGEV antigen. Immunohistochemistry provides a method to detect TGEV and possibly other closely related coronaviruses such as porcine respiratory coronavirus in situ. A diagnostic test using the same fixed tissues processed for histopathology provides veterinary practitioners an alternative to delivering live pigs or refrigerated fresh intestinal samples containing infectious virus to a diagnostic laboratory. Investigators can utilize this technique to retrospectively screen fixed tissues for TGEV antigen.
开发了一种免疫组织化学技术,使用固定组织原位研究传染性胃肠炎病毒(TGEV)抗原的存在和位置。对实验感染的无菌猪和普通猪以及自然感染TGEV的猪进行了检查。染色技术基于使用一组3种单克隆抗体检测TGEV的主要结构蛋白核衣壳。用接种强毒TGEV的无菌猪的福尔马林和高碘酸盐-赖氨酸-多聚甲醛(PLP)固定的肠道组织来确定最佳抗体浓度和孵育时间。肠道组织在各自的固定剂中保存6个月,按顺序在不同时间取出连续切片并嵌入石蜡块中。PLP和10%中性缓冲福尔马林是可接受的固定剂,可将TGEV核衣壳抗原性保存长达6个月。与PLP作为固定剂相比,福尔马林在保存原始组织形态方面更好,并且抗原检测效果更好。给普通杂交猪接种强毒TGEV,并在暴露后的不同天数对动物实施安乐死。暴露后第2天、第4天和第8天,肠道组织中TGEV核衣壳抗原呈阳性。免疫组织化学技术在14头先前经肠道黏膜涂片直接免疫荧光测定确认为TGEV阳性的自然感染猪的石蜡包埋储存组织中检测到了TGEV抗原,而9头经相同免疫荧光测定确认为TGEV抗原阴性的自然感染猪未显示与TGEV抗原存在一致的染色。免疫组织化学提供了一种原位检测TGEV以及可能其他密切相关冠状病毒(如猪呼吸道冠状病毒)的方法。使用为组织病理学处理的相同固定组织进行诊断测试,为兽医提供了一种替代方法,无需将活猪或含有传染性病毒的冷藏新鲜肠道样本送到诊断实验室。研究人员可以利用该技术回顾性筛查固定组织中的TGEV抗原。