Davis J K, Thorp R B, Parker R F, White H, Dziedzic D, D'Arcy J, Cassell G H
Infect Immun. 1986 Oct;54(1):194-201. doi: 10.1128/iai.54.1.194-201.1986.
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.
由肺支原体引起的鼠类呼吸道支原体病的动物模型为研究由感染因子导致的呼吸道疾病提供了绝佳机会。本研究的目的是开发并表征一种用于在小鼠中产生鼠类呼吸道支原体病的气溶胶模型。将小鼠在仅鼻吸入舱中用德维比斯45型雾化器产生的气溶胶暴露30分钟,可始终重现典型病变。该舱以5.0磅/平方英寸的压力运行,雾化器气流为5.3升/分钟,稀释气流为20升/分钟,雾化器中含有5毫升活的肺支原体生物体悬浮液(浓度在6×10⁵至6×10¹⁰CFU/毫升之间)。中位空气动力学直径小于4.0微米、几何标准偏差约为2.0的感染性气溶胶颗粒到达肺部,并均匀分布在不同肺叶中。肺支原体悬浮液的活力至少有1.5个对数级的损失。除50%致死剂量外,先前通过鼻内接种确定的所有参数都可以用气溶胶模型进行检测。气溶胶模型的主要优点是暴露的可重复性极佳(在不同实验之间以及在给定实验中的动物之间)、无需麻醉以及能够立即将大多数生物体沉积在肺部。唯一的缺点是需要大量的支原体培养物。