Integrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery

被引:122
作者
Kim, Hyun Uk [3 ]
Kim, Soo Young [1 ,2 ]
Jeong, Haeyoung [4 ]
Kim, Tae Yong [3 ,5 ]
Kim, Jae Jong
Choy, Hyon E. [6 ]
Yi, Kyu Yang [7 ]
Rhee, Joon Haeng [1 ,2 ,6 ]
Lee, Sang Yup [3 ,8 ,9 ]
机构
[1] Chonnam Natl Univ, Inst Vibrio Infect, Hwasun 519809, South Korea
[2] Chonnam Natl Univ, Clin Vaccine R&D Ctr, Hwasun 519809, South Korea
[3] Korea Adv Inst Sci & Technol, Metab & Biomol Engn Natl Res Lab, Dept Chem & Biomol Engn,Program BK21, Ctr Syst & Synthet Biotechnol,Inst BioCentury, Taejon 305701, South Korea
[4] Korea Res Inst Biosci & Biotechnol, Ind Biotechnol & Bioenergy Res Ctr, Taejon, South Korea
[5] GenoTech Corp, Taejon, South Korea
[6] Chonnam Natl Univ, Sch Med, Dept Microbiol, Kwangju 501757, South Korea
[7] Korea Res Inst Chem Technol, Bioorgan Sci Div, Taejon 305606, South Korea
[8] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, BioProc Engn Res Ctr, Taejon 305701, South Korea
[9] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Bioinformat Res Ctr, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
drug discovery; drug targeting; genome analysis; metabolic network; Vibrio vulnificus; ESCHERICHIA-COLI; RECONSTRUCTION; IDENTIFICATION; SEQUENCE; ENZYMES; GENE; ROBUSTNESS; RESISTANCE; TRANSPORT; PYROPHOSPHOKINASE;
D O I
10.1038/msb.2010.115
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although the genomes of many microbial pathogens have been studied to help identify effective drug targets and novel drugs, such efforts have not yet reached full fruition. In this study, we report a systems biological approach that efficiently utilizes genomic information for drug targeting and discovery, and apply this approach to the opportunistic pathogen Vibrio vulnificus CMCP6. First, we partially re-sequenced and fully re-annotated the V. vulnificus CMCP6 genome, and accordingly reconstructed its genome-scale metabolic network, VvuMBEL943. The validated network model was employed to systematically predict drug targets using the concept of metabolite essentiality, along with additional filtering criteria. Target genes encoding enzymes that interact with the five essential metabolites finally selected were experimentally validated. These five essential metabolites are critical to the survival of the cell, and hence were used to guide the cost-effective selection of chemical analogs, which were then screened for antimicrobial activity in a whole-cell assay. This approach is expected to help fill the existing gap between genomics and drug discovery. Molecular Systems Biology 7: 460; published online 18 January 2011; doi:10.1038/msb.2010.115
引用
收藏
页数:15
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