Mosier D A, Panciera R J, Rogers D P, Uhlich G A, Butine M D, Confer A W, Basaraba R J
Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manahattan 66506, USA.
Can J Vet Res. 1998 Jul;62(3):178-82.
Vaccine development for the prevention of pneumonic pasteurellosis remains a critical issue for the feedlot industry. Most currently available Pasteurella vaccines are formulated to stimulate immunity by either providing an adequate antigenic mass in the administered dose, or by relying on subsequent production of antigens by in vivo growth of live organisms. The ability of these different types of vaccines to stimulate rapid and high titres to key antigens is a key factor that will influence subsequent resistance to disease. The serologic and protective responses to a streptomycin-dependent, modified-live vaccine and a killed (bacterin-toxoid) vaccine against experimental pneumonic pasteurellosis were compared. Calves were vaccinated with a single injection of either a test vaccine or phosphate-buffered saline, challenged 14 d later by transthoracic injection with Pasteurella haemolytica, and euthanized 3 d post-challenge to evaluate the severity of pneumonia. On days 0, 7, and 14, serologic responses to various P. haemolytica antigens, including cell-associated and soluble antigens, were determined by enzyme-linked immunosorbent assays, and anti-leukotoxin antibody levels were determined by leukotoxin neutralization. The bacterin-toxoid elicited significantly greater serologic responses compared to controls for all antigens. The modified-live vaccine elicited a significantly greater response compared to controls for a whole-cell antigen preparation. Lesion scores were significantly smaller (greater protection) in calves that received the bacterin-toxoid, but not the modified-live vaccine, compared to controls.
开发用于预防肺炎巴氏杆菌病的疫苗仍然是育肥牛行业的一个关键问题。目前大多数可用的巴氏杆菌疫苗的配方是通过在给药剂量中提供足够的抗原量,或依靠活生物体在体内生长随后产生抗原,来刺激免疫力。这些不同类型的疫苗刺激产生针对关键抗原的快速和高滴度抗体的能力,是影响后续抗病性的一个关键因素。比较了一种依赖链霉素的改良活疫苗和一种灭活(细菌类毒素)疫苗对实验性肺炎巴氏杆菌病的血清学和保护性反应。给犊牛单次注射试验疫苗或磷酸盐缓冲盐水,14天后经胸腔注射溶血巴氏杆菌进行攻毒,攻毒后3天实施安乐死以评估肺炎的严重程度。在第0、7和14天,通过酶联免疫吸附测定法测定对各种溶血巴氏杆菌抗原(包括细胞相关抗原和可溶性抗原)的血清学反应,并通过白细胞毒素中和法测定抗白细胞毒素抗体水平。与对照组相比,细菌类毒素对所有抗原均引发了显著更强的血清学反应。与对照组相比,改良活疫苗对全细胞抗原制剂引发了显著更强的反应。与对照组相比,接受细菌类毒素而非改良活疫苗的犊牛的病变评分显著更小(保护作用更强)。