Bartlett M S, Fishman J A, Queener S F, Durkin M M, Jay M A, Smith J W
Department of Pathology, Indiana University School of Medicine, Indianapolis 46223.
J Clin Microbiol. 1988 Jun;26(6):1100-2. doi: 10.1128/jcm.26.6.1100-1102.1988.
Rats free of latent Pneumocystis carinii organisms were immunosuppressed with adrenal corticosteroids and transtracheally injected with P. carinii. These animals subsequently developed P. carinii pneumonia. Infection was accomplished by using organisms from infected rat lung or from culture. Diffuse infection was produced with no significant differences in the numbers of organisms found in various lobes of the lungs. Infections progressed over time so that by 6 weeks postinoculation all animals were heavily infected. Infection by transtracheal injection has three advantages over current models. First, transtracheal injection provides a reliable model which is not dependent on naturally occurring latent Pneumocystis infection. Second, transtracheal injection allows the perpetuation of specific Pneumocystis strains. Third, transtracheal injection is a more rapid and economical means of producing severe Pneumocystis pneumonia.
对无卡氏肺孢子虫潜伏性生物体的大鼠,用肾上腺皮质类固醇进行免疫抑制,并经气管注射卡氏肺孢子虫。这些动物随后患上了卡氏肺孢子虫肺炎。感染是通过使用来自受感染大鼠肺或培养物中的生物体来完成的。产生了弥漫性感染,在肺的各个叶中发现的生物体数量没有显著差异。感染随时间进展,以至于在接种后6周时所有动物都受到严重感染。与当前模型相比,经气管注射感染有三个优点。第一,经气管注射提供了一个可靠的模型,该模型不依赖于自然发生的潜伏性肺孢子虫感染。第二,经气管注射允许特定肺孢子虫菌株的延续。第三,经气管注射是产生严重卡氏肺孢子虫肺炎的一种更快速且经济的方法。