Time-Resolved Metabolic Footprinting for Nonlinear Modeling of Bacterial Substrate Utilization

被引:41
作者
Behrends, Volker [1 ,2 ]
Ebbels, Tim M. D. [1 ]
Williams, Huw D. [2 ]
Bundy, Jacob G. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Biomol Med, Div Surg Oncol Reprod Biol & Anaesthet, Fac Med, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Life Sci, Div Biol, Fac Nat Sci, London SW7 2AZ, England
关键词
BURKHOLDERIA-CEPACIA COMPLEX; PSEUDOMONAS-AERUGINOSA; ESCHERICHIA-COLI; FUNCTIONAL GENOMICS; MASS-SPECTROMETRY; SYSTEMS BIOLOGY; DRUG TOXICITY; YEAST MUTANTS; GENE; SPECTROSCOPY;
D O I
10.1128/AEM.01742-08
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Untargeted profiling of small-molecule metabolites from microbial culture supernatants (metabolic footprinting) has great potential as a phenotyping tool. We used time-resolved metabolic footprinting to compare one Escherichia coli and three Pseudomonas aeruginosa strains growing on complex media and show that considering metabolite changes over the whole course of growth provides much more information than analyses based on data from a single time point. Most strikingly, there was pronounced selectivity in metabolite uptake, even when the bacteria were growing apparently exponentially, with certain groups of metabolites not taken up until others had been entirely depleted from the medium. In addition, metabolite excretion showed some complex patterns. Fitting nonlinear equations (four-parameter sigmoids) to individual metabolite data allowed us to model these changes for metabolite uptake and visualize them by back-projecting the curve-fit parameters onto the original growth curves. These "uptake window" plots clearly demonstrated strain differences, with the uptake of some compounds being reversed in order between different strains. Comparison of an undefined rich medium with a defined complex medium designed to mimic cystic fibrosis sputum showed many differences, both qualitative and quantitative, with a greater proportion of excreted to utilized metabolites in the defined medium. Extending the strain comparison to a more closely related set of isolates showed that it was possible to discriminate two species of the Burkholderia cepacia complex based on uptake dynamics alone. We believe time-resolved metabolic footprinting could be a valuable tool for many questions in bacteriology, including isolate comparisons, phenotyping deletion mutants, and as a functional complement to taxonomic classifications.
引用
收藏
页码:2453 / 2463
页数:11
相关论文
共 63 条
[1]   High-throughput classification of yeast mutants for functional genomics using metabolic footprinting [J].
Allen, J ;
Davey, HM ;
Broadhurst, D ;
Heald, JK ;
Rowland, JJ ;
Oliver, SG ;
Kell, DB .
NATURE BIOTECHNOLOGY, 2003, 21 (06) :692-696
[2]   Discrimination of modes of action of antifungal substances by use of metabolic footprinting [J].
Allen, J ;
Davey, HM ;
Broadhurst, D ;
Rowland, JJ ;
Oliver, SG ;
Kell, DB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :6157-6165
[3]   Growth of Escherichia coli MG1655 on LB medium:: monitoring utilization of sugars, alcohols, and organic acids with transcriptional microarrays [J].
Baev, Mark V. ;
Baev, Dmitry ;
Radek, Agnes Jancso ;
Campbell, John W. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2006, 71 (03) :310-316
[4]   Metabolic profiling, metabolomic and metabonomic procedures for NMR spectroscopy of urine, plasma, serum and tissue extracts [J].
Beckonert, Olaf ;
Keun, Hector C. ;
Ebbels, Timothy M. D. ;
Bundy, Jacob G. ;
Holmes, Elaine ;
Lindon, John C. ;
Nicholson, Jeremy K. .
NATURE PROTOCOLS, 2007, 2 (11) :2692-2703
[5]   Effect of Fusarium verticillioides on maize-root-associated Burkholderia cenocepacia populations [J].
Bevivino, A ;
Peggion, V ;
Chiarini, L ;
Tabacchioni, S ;
Cantale, C ;
Dalmastri, C .
RESEARCH IN MICROBIOLOGY, 2005, 156 (10) :974-983
[6]   Potential of metabolomics as a functional genomics tool [J].
Bino, RJ ;
Hall, RD ;
Fiehn, O ;
Kopka, J ;
Saito, K ;
Draper, J ;
Nikolau, BJ ;
Mendes, P ;
Roessner-Tunali, U ;
Beale, MH ;
Trethewey, RN ;
Lange, BM ;
Wurtele, ES ;
Sumner, LW .
TRENDS IN PLANT SCIENCE, 2004, 9 (09) :418-425
[7]   Sampling for metabolome analysis of microorganisms [J].
Bolten, Christoph J. ;
Kiefer, Patrick ;
Letisse, Fabien ;
Portais, Jean-Charles ;
Wittmann, Christoph .
ANALYTICAL CHEMISTRY, 2007, 79 (10) :3843-3849
[8]   Characterization of nucleotide pools as a function of physiological state in Escherzchia coli [J].
Buckstein, Michael H. ;
He, Jian ;
Rubin, Harvey .
JOURNAL OF BACTERIOLOGY, 2008, 190 (02) :718-726
[9]   Evaluation of predicted network modules in yeast metabolism using NMR-based metabolite profiling [J].
Bundy, Jacob G. ;
Papp, Balazs ;
Harmston, Rebecca ;
Browne, Roy A. ;
Clayson, Edward M. ;
Burton, Nicola ;
Reece, Richard J. ;
Oliver, Stephen G. ;
Brindle, Kevin M. .
GENOME RESEARCH, 2007, 17 (04) :510-519
[10]   Discrimination of pathogenic clinical isolates and laboratory strains of Bacillus cereus by NMR-based metabolomic profiling [J].
Bundy, JG ;
Willey, TL ;
Castell, RS ;
Ellar, DJ ;
Brindle, KM .
FEMS MICROBIOLOGY LETTERS, 2005, 242 (01) :127-136