Westfall J A, Chatterjee A, Anderson N V
Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan 66506-5602.
J Submicrosc Cytol Pathol. 1994 Jan;26(1):41-50.
The ultrastructural changes in pulmonary alveoli produced by transtracheal inoculation of 10(6) and 10(8) CFU of Actinobacillus pleuropneumoniae serotype 5 in gnotobiotic piglets were studied after 1 and 4 h. At 1 h postinoculation (p.i.) with 10(6) or 10(8) CFU, no gross change in lung and no evidence of infiltration of cells into alveoli was observed. At 4 h p.i., at a dose of 10(6) CFU, a generalized red mottling occurred in the dorsal half of the caudal lobe, which revealed ultrastructural evidence of neutrophil infiltration into alveoli along with fibrin and a few erythrocytes. At 4 h p.i., at a dose of 10(8) CFU, there was a bilateral lung lesion characterized by a generalized mottling and congestion, within which we observed ultrastructural evidence of bacteria and cellular debris in the alveoli and fibrin clots and cellular necrosis in the alveolar septum. By using gnotobiotic piglets and visualizing the effects of bacterial inoculum on cellular ultrastructure of the lung, we have demonstrated that both dose and time play roles in the early pathogenesis of experimental porcine pleuropneumonia. The developing lesion in lungs of gnotobiotic piglets infected with pure cultures of A. pleuropneumoniae can be controlled experimentally. This experimental procedure can provide a base of reproducible, sequential, ultrastructural changes with which to compare the role of inflammatory mediators in the lung and the effects of drugs on immunologic events in the lung.
研究了在无菌仔猪经气管接种10⁶和10⁸CFU胸膜肺炎放线杆菌5型后1小时和4小时肺泡的超微结构变化。接种10⁶或10⁸CFU后1小时,未观察到肺部有肉眼可见的变化,也没有细胞浸润到肺泡的迹象。接种后4小时,剂量为10⁶CFU时,尾叶背侧半部出现广泛的红色斑点,显示有中性粒细胞浸润到肺泡的超微结构证据,伴有纤维蛋白和少量红细胞。接种后4小时,剂量为10⁸CFU时,出现双侧肺部病变,特征为广泛的斑点和充血,在其中我们观察到肺泡内有细菌和细胞碎片、纤维蛋白凝块以及肺泡间隔细胞坏死的超微结构证据。通过使用无菌仔猪并观察细菌接种物对肺细胞超微结构的影响,我们证明了剂量和时间在实验性猪胸膜肺炎的早期发病机制中都起作用。感染胸膜肺炎放线杆菌纯培养物的无菌仔猪肺部发展中的病变可以通过实验进行控制。这个实验程序可以提供可重复的、连续的超微结构变化基础,用以比较炎症介质在肺中的作用以及药物对肺免疫事件的影响。