Stephenson E H, Trahan C J, Ezzell J W, Mitchell W C, Abshire T G, Oland D D, Nelson G O
United States Army Medical Research Institute of Infectious Diseases (USAMRIID) Fort Detrick, Frederick, MD 21701-5011.
Lab Anim. 1989 Jul;23(3):261-9. doi: 10.1258/002367789780810581.
Bordetella bronchiseptica is known to be endemic in many guineapig (Cavia porcellus) colonies, and periodically is the aetiological agent of fatal epizootics of bronchopneumonia. A commercial, non-adjuvant B. bronchiseptica bacterin, which is approved for use in canines, was evaluated for induction of a protective immune response in Strain 13/N guineapigs against an airborne challenge of virulent B. bronchispeptica in small-particle aerosol. Seronegative animals were vaccinated on days 0 and 21 with intramuscular injections of 0.2 ml of bacterin. Humoral antibody titres of the vaccinated animals, as determined by ELISA, ranged from 128-1024 on day 49. On day 30 following the second dose of bacterin (study day 51), 12 vaccinated and 12 PBS sham-vaccinated animals were exposed to an inhaled dose of 4.3 x 10(5) CFU of B. bronchiseptica (325 LD50). Vaccinated, challenged animals remained clinically normal, although each guineapig did develop a localized upper respiratory infection. The rate of weight gain as well as rectal temperature of these animals were analogous to those exhibited by the control groups. Examination of 4 of the vaccinated, challenged animals on day 7 after exposure showed bacteria present in moderate to high numbers in the larynx and trachea but only minimally detectable in the lungs; by 30 days after exposure, the numbers of bacteria in the larynx and trachea were diminished, with none being detected in the lungs. Pathological alterations induced by B. bronchiseptica were not detected at either day 7 or day 30 after challenge in any of the vaccinated, challenged animals. Protection induced in Strain 13/N guineapigs by the commercial canine bacterin was sufficient to preclude the development of pulmonary disease, even in animals presented with a massive challenge of virulent bacteria in a small-particle aerosol.
支气管败血波氏杆菌在许多豚鼠(豚鼠属)群体中呈地方流行性,并且周期性地成为支气管肺炎致命性 epizootics 的病原体。一种用于犬类的市售非佐剂支气管败血波氏杆菌菌苗,被评估在 13/N 品系豚鼠中诱导针对小颗粒气溶胶中强毒支气管败血波氏杆菌空气传播攻击的保护性免疫反应。血清阴性动物在第 0 天和第 21 天通过肌肉注射 0.2 ml 菌苗进行接种。通过 ELISA 测定,接种动物的体液抗体滴度在第 49 天范围为 128 - 1024。在第二次接种菌苗后第 30 天(研究第 51 天),12 只接种疫苗和 12 只接种 PBS 假疫苗的动物暴露于吸入剂量为 4.3×10(5) CFU 的支气管败血波氏杆菌(325 LD50)。接种疫苗并受到攻击的动物临床症状正常,尽管每只豚鼠确实发生了局部上呼吸道感染。这些动物的体重增加率以及直肠温度与对照组表现相似。在暴露后第 7 天对 4 只接种疫苗并受到攻击的动物进行检查,发现喉部和气管中有中到大量细菌,但在肺部仅可微量检测到;到暴露后 30 天,喉部和气管中的细菌数量减少,肺部未检测到细菌。在任何接种疫苗并受到攻击的动物中,在攻击后第 7 天或第 30 天均未检测到支气管败血波氏杆菌引起的病理改变。市售犬用菌苗在 13/N 品系豚鼠中诱导的保护作用足以预防肺部疾病的发生,即使在动物受到小颗粒气溶胶中高毒力细菌的大量攻击时也是如此。