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铜绿假单胞菌在小鼠肺部的复制率。

Replication rate of Pseudomonas aeruginosa in the murine lung.

作者信息

Sordelli D O, Cerquetti M C, Hooke A M

出版信息

Infect Immun. 1985 Nov;50(2):388-91. doi: 10.1128/iai.50.2.388-391.1985.

Abstract

Using a method recently developed at our laboratory, we determined the initial rate of Pseudomonas aeruginosa replication in the lung under different experimental conditions. Mice were exposed to aerosols containing mixtures of a temperature-sensitive (ts) mutant of P. aeruginosa and its parental wild type (wt). The changes in the ratio of ts:wt were determined by quantitatively culturing homogenates of lungs from animals sacrificed over different time periods. The doubling time (DT) was calculated as the reciprocal of the slope of the linear portion of the curve generated by plotting n = (log [r0/rt])/log 2 against time where r is the ratio of ts:wt at a given time. The DTs measured in both outbred ICR mice and F1 hybrids (DBA/2J X B10.D2/nSnJ) were 32 and 30 min, respectively. These DTs were higher than that determined in the peritoneal cavities of ICR mice (20 min). The DT in the lungs of ICR mice rendered granulocytopenic by treatment with cyclophosphamide was 16 min. Experiments performed with inocula of different sizes showed that DTs tended to be higher in animals aerosolized with low doses of the ts-wt mixture.

摘要

我们使用本实验室最近开发的一种方法,测定了在不同实验条件下铜绿假单胞菌在肺部的初始复制速率。将小鼠暴露于含有温度敏感(ts)突变型铜绿假单胞菌及其亲本野生型(wt)混合物的气溶胶中。通过对在不同时间段处死的动物的肺匀浆进行定量培养,来确定ts:wt的比例变化。加倍时间(DT)的计算方法是,将n = (log [r0/rt])/log 2对时间作图所生成曲线线性部分斜率的倒数,其中r是给定时间的ts:wt比例。在远交ICR小鼠和F1杂种(DBA/2J×B10.D2/nSnJ)中测得的加倍时间分别为32分钟和30分钟。这些加倍时间高于在ICR小鼠腹腔中测得的加倍时间(20分钟)。经环磷酰胺处理导致粒细胞减少的ICR小鼠肺部的加倍时间为16分钟。用不同大小接种物进行的实验表明,用低剂量ts-wt混合物雾化处理的动物的加倍时间往往更高。

相似文献

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Quantitative determination of bacterial replication in vivo.体内细菌复制的定量测定。
Infect Immun. 1985 Aug;49(2):424-7. doi: 10.1128/iai.49.2.424-427.1985.

本文引用的文献

1
An apparatus for the study of airborne infection.一种用于研究空气传播感染的装置。
J Hyg (Lond). 1952 Mar;50(1):53-68. doi: 10.1017/s0022172400019422.
9
Pulmonary clearance of Pseudomonas aeruginosa.
J Lab Clin Med. 1970 Oct;76(4):548-59.

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