Hensel A, Stockhofe-Zurwieden N, Ganter M, Petzoldt K
Institute of Microbiology and Genetics, Biocentre, University of Vienna, Austria.
Vet Microbiol. 1995 Nov;47(1-2):27-41. doi: 10.1016/0378-1135(95)00106-k.
A dose-defined nose-only inhalation system for pigs was used to study the immunogenic and protective potentials of a single aerosol application of viable or killed Actinobacillus pleuropneumoniae serotype 9. Respiratory volumes were measured for each pig to calculate inhaled individual doses. Eight pigs inhaled 107 CFU A. pleuropneumoniae CVI 13261 reference strain for serotype 9. Another eight pigs received an identical dose of killed actinobacilli. After three weeks the pigs and nonexposed controls were challenged with 108 CFU of the homologous strain by aerosol. Bronchoalveolar lavage (BALF) in pigs was performed during the experiment to obtain lavage samples for assessment of local antibodies. Isotype-specific antibody responses in serum and BAL fluids were measured by ELISAs based on whole-cell antigens. The protective efficacy of aerosol immunization was evaluated by clinical and post-mortem examinations. The controls developed fever and severe pleuropneumonia, whereas previously exposed pigs had less fever and less extensive gross pulmonary lesions. After the first aerosol exposure pulmonary IgM, and IgG antibodies reactive with A. pleuropneumoniae increased significantly in both aerosol exposed groups. IgA in BALF and serum concentrations of each Ig class were significantly increased in the group exposed to viable bacteria when compared to the non-exposed controls. After aerosol challenge a pronounced increase of systemic and pulmonary IgA, IgM, and IgG antibodies was detected in both exposure groups. Aerosol application of whole-cell A. pleuropneumoniae bacterins induced similar protective effects against aerosol challenge infection as administration of an identical dose of viable bacteria. Inhalation of A. pleuropneumoniae may lead to asymptomatic carriers in some pigs that could spread the disease under field conditions.
使用一种针对猪的剂量确定的仅经鼻吸入系统,研究单次气溶胶应用活的或灭活的胸膜肺炎放线杆菌9型的免疫原性和保护潜力。测量每头猪的呼吸量以计算吸入的个体剂量。八头猪吸入107 CFU胸膜肺炎放线杆菌CVI 13261 9型参考菌株。另外八头猪接受相同剂量的灭活放线杆菌。三周后,对这些猪和未接触的对照猪通过气溶胶用108 CFU同源菌株进行攻毒。在实验期间对猪进行支气管肺泡灌洗(BALF)以获得灌洗样本用于评估局部抗体。基于全细胞抗原,通过酶联免疫吸附测定法(ELISA)测量血清和BAL液中的同型特异性抗体反应。通过临床和尸检评估气溶胶免疫的保护效果。对照猪出现发热和严重的胸膜肺炎,而先前接触过的猪发热较轻且肺部大体病变范围较小。首次气溶胶暴露后,两个气溶胶暴露组中与胸膜肺炎放线杆菌反应的肺IgM和IgG抗体均显著增加。与未接触对照相比,接触活菌组的BALF中的IgA和各Ig类别的血清浓度显著增加。气溶胶攻毒后,两个暴露组中均检测到全身和肺部IgA、IgM和IgG抗体显著增加。气溶胶应用全细胞胸膜肺炎放线杆菌菌苗诱导的针对气溶胶攻毒感染的保护效果与给予相同剂量的活菌相似。吸入胸膜肺炎放线杆菌可能导致一些猪成为无症状携带者,在野外条件下可能传播疾病。