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革兰氏阴性菌和革兰氏阳性菌感染在小鼠模型中引发不同的代谢反应。

Gram-negative and Gram-positive bacterial infections give rise to a different metabolic response in a mouse model.

作者信息

Hoerr Verena, Zbytnuik Lori, Leger Caroline, Tam Patrick P C, Kubes Paul, Vogel Hans J

机构信息

Biochemistry Research Group, Department of Biological Sciences, ‡Department of Physiology and Biophysics, Snyder Institute, University of Calgary , Calgary, Alberta T2N 1N4, Canada.

出版信息

J Proteome Res. 2012 Jun 1;11(6):3231-45. doi: 10.1021/pr201274r. Epub 2012 May 3.

Abstract

Metabolomics has become an important tool to study host-pathogen interactions and to discover potential novel therapeutic targets. In an attempt to develop a better understanding of the process of pathogenesis and the associated host response we have used a quantitative (1)H NMR approach to study the metabolic response to different bacterial infections. Here we describe that metabolic changes found in serum of mice that were infected with Staphylococcus aureus, Streptococcus pneumoniae, Escherichia coli and Pseudomonas aeruginosa can distinguish between infections caused by Gram-positive and Gram-negative bacterial strains. By combining the results of the mouse study with those of bacterial footprinting culture experiments, bacterially secreted metabolites could be identified as potential bacterium-specific biomarkers for P. aeruginosa infections but not for the other strains. Multivariate statistical analysis revealed correlations between metabolic, cytokine and physiological responses. In TLR4 and TLR2 knockout mice, host-response pathway correlated metabolites could be identified and allowed us for the first time to distinguish between bacterial- and host-induced metabolic changes. Since Gram-positive and Gram-negative bacteria activate different receptor pathways in the host, our results suggest that it may become possible in the future to use a metabolomics approach to improve on current clinical microbiology diagnostic methods.

摘要

代谢组学已成为研究宿主-病原体相互作用以及发现潜在新型治疗靶点的重要工具。为了更好地理解发病机制过程及相关的宿主反应,我们采用定量氢核磁共振方法来研究对不同细菌感染的代谢反应。在此,我们描述了感染金黄色葡萄球菌、肺炎链球菌、大肠杆菌和铜绿假单胞菌的小鼠血清中发现的代谢变化能够区分革兰氏阳性菌和革兰氏阴性菌引起的感染。通过将小鼠研究结果与细菌足迹培养实验结果相结合,细菌分泌的代谢产物可被鉴定为铜绿假单胞菌感染的潜在细菌特异性生物标志物,但其他菌株则不然。多变量统计分析揭示了代谢、细胞因子和生理反应之间的相关性。在Toll样受体4(TLR4)和Toll样受体2(TLR2)基因敲除小鼠中,可以鉴定出宿主反应途径相关的代谢产物,这使我们首次能够区分细菌诱导和宿主诱导的代谢变化。由于革兰氏阳性菌和革兰氏阴性菌在宿主中激活不同的受体途径,我们的结果表明,未来有可能使用代谢组学方法来改进当前的临床微生物诊断方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de1d/3368387/a18e8e997d6a/pr-2011-01274r_0002.jpg

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