肺部对溶血性巴氏杆菌和多杀性巴氏杆菌气管内攻击的反应。

T R Ames, R J Markham, J Opuda-Asibo, J R Leininger, S K Maheswaran
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引用次数: 0

摘要

犊牛气管内接种5 × 10(7)、5 × 10(8)或5 × 10(9)集落形成单位的溶血巴氏杆菌固定期培养18小时或对数期培养4小时。与相应的固定相培养相比,所有浓度的对数相培养在死后检查中产生了更严重的临床症状、血液学变化和肺部病变。剂量越大,效果越严重,尤其是对数相培养。伴局灶性或多灶性坏死的纤维性支气管肺炎在固定期和对数期培养中一致产生。为了确定这种病变是溶血假单胞菌特有的,还是可以由快速生长的革兰氏阴性菌普遍产生,采用与溶血假单胞菌培养相同的方法制备了4小时对数相多杀性巴氏杆菌培养物,并以高细菌剂量(5 X 10[9])给小牛气管内注射。溶血假单胞菌比多杀假单胞菌产生更严重的临床、血液学和形态学变化。多杀性假单胞菌的病变与溶血假单胞菌的病变形态不同;多杀性假单胞菌有化脓性渗出成分,很少或没有坏死。似乎一个重要的致病原理是由快速生长的溶血假单胞菌产生的,它导致比多杀性假单胞菌产生更严重的临床疾病和更多的坏死性肺病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary response to intratracheal challenge with Pasteurella haemolytica and Pasteurella multocida.

Calves were inoculated intratracheally with 5 X 10(7), 5 X 10(8), or 5 X 10(9) colony forming units of either 18-hour stationary phase cultures or 4-hour log phase cultures of Pasteurella haemolytica. The log phase culture at all concentrations produced more severe clinical signs, hematological changes and pulmonary lesions at postmortem examination than did the corresponding stationary phase culture. More severe effects were seen with the larger doses especially with the log phase culture. Fibrinous bronchopneumonia with focal or multifocal necrosis was consistently produced by both the stationary and log phase cultures. To determine if this lesion was peculiar to P. haemolytica or whether it could be produced generally by rapidly growing Gram negative organisms, a 4-hour log phase culture of Pasteurella multocida was prepared in an identical manner to that used for the culture of P. haemolytica and given to calves intratracheally at the high bacterial dose (5 X 10(9]. The P. haemolytica produced more severe clinical, hematological and morphological changes than did the P. multocida. The lesions observed with P. multocida differed morphologically from those of P. haemolytica; there was a suppurative exudative component and minimal to no necrosis with P. multocida. It appears that an important pathogenic principle is produced by the rapidly growing P. haemolytica that causes it to produce a more severe clinical disease and more necrotizing pulmonary lesions than P. multocida.

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