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本文引用的文献

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Epidemiology of Burkholderia cepacia complex in patients with cystic fibrosis, Canada.加拿大囊性纤维化患者中洋葱伯克霍尔德菌复合体的流行病学
Emerg Infect Dis. 2002 Feb;8(2):181-7. doi: 10.3201/eid0802.010163.
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Mouse models of cystic fibrosis.
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Enhanced susceptibility to pulmonary infection with Burkholderia cepacia in Cftr(-/-) mice.Cftr基因敲除小鼠对洋葱伯克霍尔德菌肺部感染的易感性增强。
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Invasion of murine respiratory epithelial cells in vivo by Burkholderia cepacia.洋葱伯克霍尔德菌对小鼠呼吸道上皮细胞的体内侵袭
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Mouse models of chronic lung infection with Pseudomonas aeruginosa: models for the study of cystic fibrosis.铜绿假单胞菌慢性肺部感染的小鼠模型:用于囊性纤维化研究的模型
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Preferential adherence of cable-piliated burkholderia cepacia to respiratory epithelia of CF knockout mice and human cystic fibrosis lung explants.有鞭毛的洋葱伯克霍尔德菌对囊性纤维化基因敲除小鼠的呼吸道上皮细胞和人囊性纤维化肺外植体的优先黏附。
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Clinical and environmental isolates of Burkholderia cepacia exhibit differential cytotoxicity towards macrophages and mast cells.
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Cable-piliated Burkholderia cepacia binds to cytokeratin 13 of epithelial cells.具有鞭毛的洋葱伯克霍尔德菌与上皮细胞的细胞角蛋白13结合。
Infect Immun. 2000 Apr;68(4):1787-95. doi: 10.1128/IAI.68.4.1787-1795.2000.
10
Diagnostically and experimentally useful panel of strains from the Burkholderia cepacia complex.洋葱伯克霍尔德菌复合体中具有诊断和实验用途的菌株组。
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洋葱伯克霍尔德菌复合体基因组变种在肺部感染小鼠模型中的差异持续性

Differential persistence among genomovars of the Burkholderia cepacia complex in a murine model of pulmonary infection.

作者信息

Chu Karen K, Davidson Donald J, Halsey T Keith, Chung Jacqueline W, Speert David P

机构信息

Department of Paediatrics, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Infect Immun. 2002 May;70(5):2715-20. doi: 10.1128/IAI.70.5.2715-2720.2002.

DOI:10.1128/IAI.70.5.2715-2720.2002
PMID:11953418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC127911/
Abstract

Cystic fibrosis patients infected with strains from different genomovars of the Burkholderia cepacia complex can experience diverse clinical outcomes. To identify genomovar-specific determinants that might be responsible for these differences, we developed a pulmonary model of infection in BALB/c mice. Mice were rendered leukopenic by administration of cyclophosphamide prior to intranasal challenge with 1.6 x 10(4) bacteria. Five of six genomovar II strains persisted at stable numbers in the lungs until day 16 with minimal toxicity, whereas zero of seven genomovar III strains persisted but resulted in variable toxicity. We have developed a chronic pulmonary model of B. cepacia infection which reveals differences among genomovars in terms of clinical infection outcome.

摘要

感染了洋葱伯克霍尔德菌复合体不同基因变种菌株的囊性纤维化患者可能会经历不同的临床结果。为了确定可能导致这些差异的基因变种特异性决定因素,我们在BALB/c小鼠中建立了一种肺部感染模型。在用1.6×10⁴个细菌进行鼻内攻击之前,通过给予环磷酰胺使小鼠白细胞减少。六个基因变种II菌株中的五个在肺部以稳定数量持续存在至第16天,毒性最小,而七个基因变种III菌株中没有一个持续存在,但导致了不同程度的毒性。我们已经建立了一种洋葱伯克霍尔德菌感染的慢性肺部模型,该模型揭示了不同基因变种在临床感染结果方面的差异。