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囊性纤维化跨膜传导调节因子基因敲除小鼠控制铜绿假单胞菌肺部感染的能力受损。

Impaired ability of Cftr knockout mice to control lung infection with Pseudomonas aeruginosa.

作者信息

Gosselin D, Stevenson M M, Cowley E A, Griesenbach U, Eidelman D H, Boulé M, Tam M F, Kent G, Skamene E, Tsui L C, Radzioch D

机构信息

Centre for the Study of Host Resistance, McGill University, Montreal, Quebec, Canada.

出版信息

Am J Respir Crit Care Med. 1998 Apr;157(4 Pt 1):1253-62. doi: 10.1164/ajrccm.157.4.9702081.

Abstract

The present study was aimed at investigating the innate susceptibility of C57BL/6-Cftrunc/Cftrunc knockout [B6-Cftr (-/-)] mice to pulmonary infection with Pseudomonas aeruginosa. Our results indicate that 58.4% of B6-Cftr (-/-) mice died within 6 d following lung infection with 10(5) P. aeruginosa entrapped in agar beads, whereas only 12.1% of B6-Cftr (+/+) mice died over the same period of time. Moreover, the number of bacteria recovered from the lungs of B6-Cftr (-/-) mice 3 and 6 d after infection was significantly higher than that observed in their littermate controls. No correlation was found between the weight or age of the animals and the number of viable bacteria recovered from the lungs of mice. Histopathological examination of lung sections from P. aeruginosa-infected mice revealed that the infection results in a severe bronchopneumonia. Both B6-Cftr (-/-) knockout mice and their littermate controls developed similar lung pathology during the course of infection. Overall, results reported in the present study suggest that a defect at the Cftr locus leads to an exacerbation of P. aeruginosa lung infection resulting in a dramatically increased mortality rate and higher bacterial load.

摘要

本研究旨在调查C57BL/6-Cftrunc/Cftrunc基因敲除[B6-Cftr (-/-)]小鼠对铜绿假单胞菌肺部感染的天然易感性。我们的结果表明,58.4%的B6-Cftr (-/-)小鼠在经琼脂珠包裹的10(5)个铜绿假单胞菌肺部感染后6天内死亡,而同期只有12.1%的B6-Cftr (+/+)小鼠死亡。此外,感染后3天和6天从B6-Cftr (-/-)小鼠肺部回收的细菌数量显著高于其同窝对照小鼠。未发现动物的体重或年龄与从小鼠肺部回收的活菌数量之间存在相关性。对铜绿假单胞菌感染小鼠的肺组织切片进行组织病理学检查发现,感染导致严重的支气管肺炎。在感染过程中,B6-Cftr (-/-)基因敲除小鼠及其同窝对照小鼠出现了相似的肺部病理变化。总体而言,本研究报告的结果表明,Cftr基因座的缺陷导致铜绿假单胞菌肺部感染加剧,从而导致死亡率显著增加和细菌载量升高。

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