Welch S K, Saif L J, Ram S
Department of Veterinary Preventive Medicine, Ohio State University, Wooster 44691.
Am J Vet Res. 1988 Aug;49(8):1228-34.
Two litters of suckling pigs seronegative for transmissible gastroenteritis (TGE) virus were orally inoculated with live attenuated (P115) or virulent (M5C) strains of TGE virus. A third seronegative litter (controls) was given cell culture fluids from uninfected cells. Lymphocytes were collected from blood, spleen, mesenteric lymph nodes, and Peyer patches of euthanatized pigs at 0 day and approximately weekly until 26 days after exposure and at approximately 45 days after exposure. Sera were tested for virus-neutralizing antibody titers by use of plaque reduction. Lymphocytes were tested in a lymphocyte proliferation assay for uptake of [3H]thymidine after incubation with the homologous or the heterologous strain of inactivated TGE virus or uninfected cell culture fluids. Only pigs inoculated with virulent TGE virus developed clinical signs of TGE and shed virus. However, all pigs inoculated with TGE virus seroconverted at 6 days after exposure. Responses of lymphocytes from all sources from TGE virus-inoculated pigs peaked between 6 and 14 days after exposure. Pigs inoculated with virulent TGE virus had higher lymphocyte proliferative responses and neutralizing antibody titers than did pigs inoculated with attenuated TGE virus. Cessation of virus shedding coincided with the peak of lymphocyte proliferative responses. The highest responses were with intestinal lymphocytes (mesenteric lymph nodes and Peyer patches) from pigs inoculated with virulent TGE virus. The responses of intestinal lymphocytes from pigs inoculated with attenuated virus were not significantly different from those of pigs inoculated with cell culture fluid. Lymphocytes collected from all sources, except blood from M5C-inoculated pigs, had significantly (P less than 0.05) higher responses to the homologous than to the heterologous TGE virus stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)
将两窝对传染性胃肠炎(TGE)病毒血清学阴性的哺乳仔猪经口接种TGE病毒的弱毒(P115)或强毒(M5C)毒株。第三窝血清学阴性仔猪(对照组)给予未感染细胞的细胞培养液。在暴露后0天、约每周一次直至暴露后26天以及暴露后约45天,从安乐死猪的血液、脾脏、肠系膜淋巴结和派伊尔结收集淋巴细胞。通过蚀斑减少法检测血清中的病毒中和抗体滴度。在淋巴细胞增殖试验中,将淋巴细胞与灭活的TGE病毒同源或异源毒株或未感染细胞培养液孵育后,检测其对[3H]胸腺嘧啶核苷的摄取情况。只有接种强毒TGE病毒的仔猪出现TGE临床症状并排出病毒。然而,所有接种TGE病毒的仔猪在暴露后6天血清阳转。接种TGE病毒的猪所有来源的淋巴细胞反应在暴露后6至14天达到峰值。接种强毒TGE病毒的仔猪比接种弱毒TGE病毒的仔猪具有更高的淋巴细胞增殖反应和中和抗体滴度。病毒排出停止与淋巴细胞增殖反应峰值同时出现。最高反应出现在接种强毒TGE病毒的猪的肠道淋巴细胞(肠系膜淋巴结和派伊尔结)。接种弱毒病毒的猪的肠道淋巴细胞反应与接种细胞培养液的猪的反应无显著差异。除接种M5C的猪的血液外,从所有来源收集的淋巴细胞对同源TGE病毒刺激的反应显著(P小于0.05)高于对异源TGE病毒刺激的反应。(摘要截短至250字)