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Development of an aerosol model of murine respiratory mycoplasmosis in mice.

机译:小鼠小鼠呼吸道支原体气雾模型的建立。

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摘要

Animal models of murine respiratory mycoplasmosis due to Mycoplasma pulmonis provide excellent opportunities to study respiratory disease due to an infectious agent. The purpose of the present study was to develop and characterize an aerosol model for the production of murine respiratory mycoplasmosis in mice. The exposure of mice for 30 min to aerosols generated with a DeVilbiss 45 nebulizer in a nose-only inhalation chamber consistently reproduced typical lesions. The chamber was operated with a nebulizer air flow of 5.3 liters/min at 5.0 lb/in and a diluting air flow of 20 liters/min, with the nebulizer containing 5 ml of a suspension of viable M. pulmonis organisms (a concentration between 6 X 10(5) to 6 X 10(10) CFU/ml). Infective aerosol particles of less than a 4.0-micron median aerodynamic diameter with a geometric standard deviation of approximately 2.0 reached the lungs and were evenly distributed among the different lung lobes. A minimum 1.5-log loss of viability in the M. pulmonis suspension was demonstrated. With the exception of the 50% lethal dose, all of the parameters previously established by intranasal inoculation could be examined with the aerosol model. The major advantages of the aerosol model were excellent reproducibility of exposure (both between different experiments and between animals in a given experiment), the avoidance of anesthetization, and the ability to immediately deposit the majority of the organisms in the lung. The only disadvantage was the requirement for large volumes of mycoplasmal cultures.
机译:由于肺炎支原体引起的鼠类呼吸道支原体病的动物模型为研究由于传染原引起的呼吸道疾病提供了极好的机会。本研究的目的是开发和表征小鼠中产生小鼠呼吸道支原体病的气溶胶模型。在仅鼻子的吸入室内,将小鼠暴露于DeVilbiss 45雾化器产生的气溶胶中持续30分钟,可始终再现典型的病变。该腔室在5.0磅/英寸的条件下以5.3升/分钟的雾化器空气流量和20升/分钟的稀释空气流量进行操作,其中的雾化器包含5毫升活的肺炎支原体生物的悬浮液(浓度为6 X 10(5)至6 X 10(10)CFU / ml)。小于4.0微米平均空气动力学直径且几何标准偏差约为2.0的感染性气溶胶颗粒到达肺部,并均匀分布在不同的肺叶之间。证实了肺炎支原体悬浮液中活力的最小损失为1.5个对数。除了50%的致死剂量外,以前通过鼻内接种建立的所有参数都可以用气溶胶模型检查。气溶胶模型的主要优点是暴露的重现性极佳(在不同实验之间以及在给定实验中的动物之间),避免麻醉以及能够立即将大部分生物沉积在肺中。唯一的缺点是需要大量的支原体培养物。

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