Metabolic Network Analysis of Pseudomonas aeruginosa during Chronic Cystic Fibrosis Lung Infection

被引:71
|
作者
Oberhardt, Matthew A. [1 ]
Goldberg, Joanna B. [2 ]
Hogardt, Michael [3 ]
Papin, Jason A. [1 ]
机构
[1] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
[3] Bundeswehr Inst Microbiol, D-80937 Munich, Germany
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
CHRONIC PULMONARY INFECTION; TRANSCRIPTIONAL REGULATION; OPPORTUNISTIC PATHOGEN; GROWTH PHENOTYPES; ESCHERICHIA-COLI; MODELS; RECONSTRUCTION; MICROARRAYS; ADAPTATION; PREDICTION;
D O I
10.1128/JB.00900-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
System-level modeling is beginning to be used to decipher high throughput data in the context of disease. In this study, we present an integration of expression microarray data with a genome-scale metabolic reconstruction of Pseudomonas aeruginosa in the context of a chronic cystic fibrosis (CF) lung infection. A genome-scale reconstruction of P. aeruginosa metabolism was tailored to represent the metabolic states of two clonally related lineages of P. aeruginosa isolated from the lungs of a CF patient at different points over a 44-month time course, giving a mechanistic glimpse into how the bacterial metabolism adapts over time in the CF lung. Metabolic capacities were analyzed to determine how tradeoffs between growth and other important cellular processes shift during disease progression. Genes whose knockouts were either significantly growth reducing or lethal in silico were also identified for each time point and serve as hypotheses for future drug targeting efforts specific to the stages of disease progression.
引用
收藏
页码:5534 / 5548
页数:15
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