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Salmonella Enterica: a Surprisingly Well-adapted Intracellular Lifestyle

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Journal Front Microbiol
Specialty Microbiology
Date 2012 May 8
PMID 22563326
Citations 32
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Abstract

The infectious intracellular lifestyle of Salmonella enterica relies on the adaptation to nutritional conditions within the Salmonella-containing vacuole (SCV) in host cells. We summarize latest results on metabolic requirements for Salmonella during infection. This includes intracellular phenotypes of mutant strains based on metabolic modeling and experimental tests, isotopolog profiling using (13)C-compounds in intracellular Salmonella, and complementation of metabolic defects for attenuated mutant strains towards a comprehensive understanding of the metabolic requirements of the intracellular lifestyle of Salmonella. Helpful for this are also genomic comparisons. We outline further recent studies and which analyses of intracellular phenotypes and improved metabolic simulations were done and comment on technical required steps as well as progress involved in the iterative refinement of metabolic flux models, analyses of mutant phenotypes, and isotopolog analyses. Salmonella lifestyle is well-adapted to the SCV and its specific metabolic requirements. Salmonella metabolism adapts rapidly to SCV conditions, the metabolic generalist Salmonella is quite successful in host infection.

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References
1.
Gaudermann P, Vogl I, Zientz E, Silva F, Moya A, Gross R . Analysis of and function predictions for previously conserved hypothetical or putative proteins in Blochmannia floridanus. BMC Microbiol. 2006; 6:1. PMC: 1360075. DOI: 10.1186/1471-2180-6-1. View

2.
Thiele I, Hyduke D, Steeb B, Fankam G, Allen D, Bazzani S . A community effort towards a knowledge-base and mathematical model of the human pathogen Salmonella Typhimurium LT2. BMC Syst Biol. 2011; 5:8. PMC: 3032673. DOI: 10.1186/1752-0509-5-8. View

3.
Harvey P, Watson M, Hulme S, Jones M, Lovell M, Berchieri Jr A . Salmonella enterica serovar typhimurium colonizing the lumen of the chicken intestine grows slowly and upregulates a unique set of virulence and metabolism genes. Infect Immun. 2011; 79(10):4105-21. PMC: 3187277. DOI: 10.1128/IAI.01390-10. View

4.
Lundberg B, Wolf Jr R, Dinauer M, Xu Y, Fang F . Glucose 6-phosphate dehydrogenase is required for Salmonella typhimurium virulence and resistance to reactive oxygen and nitrogen intermediates. Infect Immun. 1998; 67(1):436-8. PMC: 96332. DOI: 10.1128/IAI.67.1.436-438.1999. View

5.
Ruppin E, Papin J, de Figueiredo L, Schuster S . Metabolic reconstruction, constraint-based analysis and game theory to probe genome-scale metabolic networks. Curr Opin Biotechnol. 2010; 21(4):502-10. DOI: 10.1016/j.copbio.2010.07.002. View