Changes in proteome of the Δhfq strain derived from Francisella tularensis LVS correspond with its attenuated phenotype

被引:6
|
作者
Lenco, Juraj [1 ]
Tambor, Vojtech [2 ]
Link, Marek [1 ]
Klimentova, Jana [1 ]
Dresler, Jiri [1 ]
Peterek, Miroslav [2 ]
Charbit, Alain [3 ,4 ]
Stulik, Jiri [1 ]
机构
[1] Univ Def, Inst Mol Pathol, Fac Mil Hlth Sci, Hradec Kralove 50001, Czech Republic
[2] Univ Hosp Hradec Kralove, Biomed Res Ctr, Hradec Kralove, Czech Republic
[3] Univ Paris 05, Paris, France
[4] CNRS, INSERM, U1151, UMR8253,Equipe Pathogenie Infect Syst 11, Paris, France
关键词
Francisella tularensis; Hfq; Mass spectrometry; Microbiology; Virulence; VIRULENCE GENE-EXPRESSION; PATHOGENICITY ISLAND; VI SECRETION; PROTEINS; IDENTIFICATION; DELETION;
D O I
10.1002/pmic.201400198
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The posttranscriptional regulatory protein Hfq was shown to be an important determinant of the stress resistance and full virulence in the dangerous human pathogen Francisella tularensis. Transcriptomics brought rather limited clues to the precise contribution of Hfq in virulence. To reveal the molecular basis of the attenuation caused by hfq inactivation, we employed iTRAQ in the present study and compared proteomes of the parent and isogenic Delta hfq strains. We show that Hfq modulates the level of 76 proteins. Most of them show decreased abundance in the Delta hfq mutant, thereby indicating that Hfq widely acts rather as a positive regulator of Francisella gene expression. Several key Francisella virulence factors including those encoded within the Francisella pathogenicity island were found among the downregulated proteins, which is in a good agreement with the attenuated phenotype of the Delta hfq strain. To further validate the iTRAQ exploratory findings, we subsequently performed targeted LC-SRM analysis of selected proteins. This accurate quantification method corroborated the trends found in the iTRAQ data.
引用
收藏
页码:2400 / 2409
页数:10
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