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开发用于研究急性和慢性类鼻疽伯克霍尔德菌肺部感染的新型动物感染模型。

Development of novel animal infection models for the study of acute and chronic Burkholderia pseudomallei pulmonary infections.

作者信息

van Schaik Erin, Tom Marina, DeVinney Rebekah, Woods Donald E

机构信息

Department of Microbiology and Infectious Diseases, Faculty of Medicine, University of Calgary Health Sciences Centre, 3330 Hospital Drive, NW, Calgary, Alberta T2N 4N1, Canada.

出版信息

Microbes Infect. 2008 Oct;10(12-13):1291-9. doi: 10.1016/j.micinf.2008.07.028. Epub 2008 Jul 29.

DOI:10.1016/j.micinf.2008.07.028
PMID:18707015
Abstract

Burkholderia pseudomallei causes the disease melioidosis. The most common clinical presentation of melioidosis is pneumonia which can occur in acute and chronic forms. The tsunami of 2004 demonstrated a new risk factor for the acquisition of melioidosis and resulted in the proposal that direct delivery of B. pseudomallei into the lungs may result in the enhanced ability of this pathogen to cause disease. In the present studies, we present the development and characterization of rat models of acute and chronic pulmonary melioidosis, and we have utilized these models to demonstrate that direct delivery of B. pseudomallei into the lungs does indeed result in the enhanced ability of this pathogen to cause disease. Importantly, the rat lung infection models for melioidosis can quantify differences in virulence between individual B. pseudomallei wild type strains during both acute and chronic infections. Further, the histopathology associated with pulmonary melioidosis in the rat resembles that seen in tuberculosis. B. pseudomallei microarrays were used to characterize gene expression patterns during chronic pulmonary infections. Transcriptional profiling at several time points during chronic infection revealed that a wide range of genes associated with virulence and metabolic functions are differentially regulated in vivo during chronic infections.

摘要

类鼻疽伯克霍尔德菌可引发类鼻疽病。类鼻疽病最常见的临床表现是肺炎,可呈急性和慢性形式。2004年的海啸显示了一种新的类鼻疽病感染风险因素,并促使人们提出将类鼻疽伯克霍尔德菌直接注入肺部可能会增强该病原体致病能力的观点。在本研究中,我们展示了急性和慢性肺类鼻疽病大鼠模型的建立及特性研究,并且我们利用这些模型证明将类鼻疽伯克霍尔德菌直接注入肺部确实会增强该病原体的致病能力。重要的是,类鼻疽病大鼠肺部感染模型能够量化不同类鼻疽伯克霍尔德菌野生型菌株在急性和慢性感染期间的毒力差异。此外,大鼠肺部类鼻疽病的组织病理学与结核病相似。利用类鼻疽伯克霍尔德菌微阵列来表征慢性肺部感染期间的基因表达模式。慢性感染期间多个时间点的转录谱分析表明,在慢性感染期间,体内多种与毒力和代谢功能相关的基因受到差异调节。

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