System-level analysis of Salmonella metabolism during infection

被引:37
作者
Bumann, Dirk [1 ]
机构
[1] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
关键词
ENTERICA SEROVAR TYPHIMURIUM; ESCHERICHIA-COLI K-12; LISTERIA-MONOCYTOGENES; GENE-EXPRESSION; MYCOBACTERIUM-TUBERCULOSIS; CARBON METABOLISM; HIGH-THROUGHPUT; ANIMAL-MODELS; VIRULENCE; HOST;
D O I
10.1016/j.mib.2009.08.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Infectious diseases represent a major threat to human health. To develop urgently needed new control strategies, a transition from research focusing on individual factors to a more integrated system-level analysis might be needed. Such an approach faces great challenges and might require development of new concepts in large-scale data analysis. Here, I discuss for the well-characterized model pathogen Salmonella, how extensively studied metabolism can be used as a training field for infection biology at the systems level. Extensive experimental data can be analyzed in context using metabolic network visualization tools and in silico modeling based on genome-scale metabolic reconstructions. Suitable approaches to obtain still missing comprehensive quantitative data on Salmonella nutrition in infected host tissues are described. Such an integrated investigation of Salmonella metabolism during infection will enable an unprecedented large-scale understanding of pathogen in vivo activities, help to evaluate concepts and strategies for system-level analysis of host/pathogen interactions in general, and provide a basis for rational development of novel antimicrobials and efficacious live vaccines.
引用
收藏
页码:559 / 567
页数:9
相关论文
共 77 条
[1]   Interplay between MgtC and PagC in Salmonella enterica serovar Typhimurium [J].
Alix, Eric ;
Miki, Tsuyoshi ;
Felix, Christine ;
Rang, Cecile ;
Figueroa-Bossi, Nara ;
Dernettre, Edith ;
Blanc-Potard, Anne-Beatrice .
MICROBIAL PATHOGENESIS, 2008, 45 (03) :236-240
[2]   The metabolic world of Escherichia coli is not small [J].
Arita, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (06) :1543-1547
[3]  
BAUMLER AJ, 1994, INFECT IMMUN, V62, P1623
[4]   Robust Salmonella metabolism limits possibilities for new antimicrobials [J].
Becker, D ;
Selbach, M ;
Rollenhagen, C ;
Ballmaier, M ;
Meyer, TF ;
Mann, M ;
Bumann, D .
NATURE, 2006, 440 (7082) :303-307
[5]   Typhoid and paratyphoid fever [J].
Bhan, MK ;
Bahl, R ;
Bhatnagar, S .
LANCET, 2005, 366 (9487) :749-762
[6]   Novel target sites in bacteria for overcoming antibiotic resistance [J].
Black, MT ;
Hodgson, J .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (10) :1528-1538
[7]   Glucose and Glycolysis Are Required for the Successful Infection of Macrophages and Mice by Salmonella enterica Serovar Typhimurium [J].
Bowden, Steven D. ;
Rowley, Gary ;
Hinton, Jay C. D. ;
Thompson, Arthur .
INFECTION AND IMMUNITY, 2009, 77 (07) :3117-3126
[8]   Complexities of targeting innate immunity to treat infection [J].
Brown, Kelly L. ;
Cosseau, Celine ;
Gardy, Jennifer L. ;
Hancock, Robert E. W. .
TRENDS IN IMMUNOLOGY, 2007, 28 (06) :260-266
[9]   Virulence strategies for infecting phagocytes deduced from the in vivo transcriptional program of Legionella pneumophila [J].
Bruggemann, Holger ;
Hagman, Arne ;
Jules, Matthieu ;
Sismeiro, Odile ;
Dillies, Marie-Agnes ;
Gouyette, Catherine ;
Kunst, Frank ;
Steinert, Michael ;
Heuner, Klaus ;
Coppee, Jean-Yves ;
Buchrieser, Carmen .
CELLULAR MICROBIOLOGY, 2006, 8 (08) :1228-1240
[10]   Examination of Salmonella gene expression in an infected mammalian host using the green fluorescent protein and two-colour flow cytometry [J].
Bumann, D .
MOLECULAR MICROBIOLOGY, 2002, 43 (05) :1269-1283