A gel-free quantitative proteomics approach to investigate temperature adaptation of the food-borne pathogen Cronobacter turicensis 3032

被引:26
作者
Carranza, Paula [1 ]
Grunau, Alexander [1 ]
Schneider, Thomas [1 ]
Hartmann, Isabel [2 ]
Lehner, Angelika [2 ]
Stephan, Roger [2 ]
Gehrig, Peter [3 ]
Grossmann, Jonas [3 ]
Groebel, Katrin [4 ]
Hoelzle, Ludwig E. [4 ]
Eberl, Leo [1 ]
Riedel, Kathrin [1 ]
机构
[1] UZH, Dept Microbiol, Inst Plant Biol, Zurich, Switzerland
[2] UZH, Inst Food Safety & Hyg, Vetsuisse Fac, Zurich, Switzerland
[3] UZH ETH, Funct Genom Ctr Zurich, Zurich, Switzerland
[4] UZH, Inst Vet Bacteriol, Zurich, Switzerland
基金
美国国家科学基金会; 瑞士国家科学基金会;
关键词
Bacterial proteomics; Cronobacter turicensis; iTRAQ; Microbiology; Physiology; Temperature adaptation; COLD SHOCK RESPONSE; INFANT MILK FORMULA; ESCHERICHIA-COLI; ENTEROBACTER-SAKAZAKII; STRESS-RESPONSE; HEAT-SHOCK; OSMOTIC-STRESS; PROTEIN-A; TRANSCRIPTIONAL RESPONSE; PHYSIOLOGICAL STRESS;
D O I
10.1002/pmic.200900460
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The opportunistic food-borne pathogen Cronobacter sp. causes rare but significant illness in neonates and is capable to grow at a remarkably wide range of temperatures from 5.5 to 47 degrees C. A gel-free quantitative proteomics approach was employed to investigate the molecular basis of the Cronobacter sp. adaptation to heat and cold-stress. To this end the model strain Cronobacter turicensis 3032 was grown at 25, 37, 44, and 47 degrees C, and whole-cell and secreted proteins were iTRAQ-labelled and identified/quantified by 2-D-LC-MALDI-TOF/TOF-MS. While 44 degrees C caused only minor changes in C. turicensis growth rate and protein profile, 47 degrees C affected the expression of about 20% of all 891 identified proteins and resulted in a reduced growth rate and rendered the strain non-motile and filamentous. Among the heat-induced proteins were heat shock factors, transcriptional and translational proteins, whereas proteins affecting cellular morphology, proteins involved in motility, central metabolism and energy production were down-regulated. Notably, numerous potential virulence factors were found to be up-regulated at higher temperatures, suggesting an elevated pathogenic potential of Cronobacter sp. under these growth conditions. Significant alterations in the protein expression profile and growth rate of C. turicensis exposed to 25 degrees C indicate that at this temperature the organism is cold-stressed. Up-regulated gene products comprised cold-shock, DNA-binding and ribosomal proteins, factors that support protein folding and proteins opposing cold-induced decrease in membrane fluidity, whereas down-regulated proteins were mainly involved in central metabolism.
引用
收藏
页码:3248 / 3261
页数:14
相关论文
共 91 条
[1]   The ribosome-associated inhibitor A reduces translation errors [J].
Agafonov, DE ;
Spirin, AS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (02) :354-358
[2]  
Agafonov DE, 2001, EMBO REP, V2, P399
[3]   Differential expression of the outer membrane protein W (OmpW) stress response in enterohemorrhagic Escherichia coli O157:H7 corresponds to the viable but non-culturable state [J].
Asakura, Hiroshi ;
Kawamoto, Keiko ;
Haishima, Yuji ;
Igimi, Shizunobu ;
Yamamoto, Shigeki ;
Makino, Sou-ichi .
RESEARCH IN MICROBIOLOGY, 2008, 159 (9-10) :709-717
[4]   Genetic characterization of thermal tolerance in Enterobacter sakazakii [J].
Asakura, Hiroshi ;
Morita-Ishihara, Tomoko ;
Yamamoto, Shigeki ;
Igimi, Shizunobu .
MICROBIOLOGY AND IMMUNOLOGY, 2007, 51 (07) :671-677
[5]   Genomewide transcriptional analysis of the cold shock response in Bacillus subtilis [J].
Beckering, CL ;
Steil, L ;
Weber, MHW ;
Völker, U ;
Marahiel, MA .
JOURNAL OF BACTERIOLOGY, 2002, 184 (22) :6395-6402
[6]   Regulation of Serratia marcescens ompF and ompC porin genes in response to osmotic stress, salicylate, temperature and pH [J].
Begic, S ;
Worobec, EA .
MICROBIOLOGY-SGM, 2006, 152 :485-491
[8]   Transcriptional profiling of the hyperthermophilic methanarchaeon Methanococcus jannaschii in response to lethal heat and non-lethal cold shock [J].
Boonyaratanakornkit, BB ;
Simpson, AJ ;
Whitehead, TA ;
Fraser, CM ;
El-Sayed, NMA ;
Clark, DS .
ENVIRONMENTAL MICROBIOLOGY, 2005, 7 (06) :789-797
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   Desiccation and heat tolerance of Enterobacter sakazakii [J].
Breeuwer, P ;
Lardeau, A ;
Peterz, M ;
Joosten, HM .
JOURNAL OF APPLIED MICROBIOLOGY, 2003, 95 (05) :967-973