Comparison of proteins expressed by Pseudomonas aeruginosa strains representing initial and chronic isolates from a cystic fibrosis patient:: an analysis by 2-D gel electrophoresis and capillary column liquid chromatography-tandem mass spectrometry

被引:136
作者
Hanna, SL
Sherman, NE
Kinter, MT
Goldberg, JB [1 ]
机构
[1] Univ Virginia, Hlth Sci Ctr, Dept Microbiol, Charlottesville, VA 22908 USA
[2] Univ Virginia, Hlth Sci Ctr, WM Keck Biomed Mass Spectrometry Lab, Biomol Res Facil, Charlottesville, VA 22908 USA
[3] Cleveland Clin Fdn, Lerner Res Inst, Dept Cell Biol, Cleveland, OH 44195 USA
来源
MICROBIOLOGY-UK | 2000年 / 146卷
关键词
genome analysis; proteomics; peptide sequencing; outer-membrane proteins; genotypic and phenotypic comparison;
D O I
10.1099/00221287-146-10-2495
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Isolates of Pseudomonas aeruginosa from chronic lung infections in cystic fibrosis (CF) patients have phenotypes distinct from those initially infecting CF patients, as well as from other clinical or environmental isolates, To gain a better understanding of the differences in these isolates, protein expression was followed using two-dimensional (2-D) gel electrophoresis and protein identification by peptide sequencing using micro-capillary column liquid chromatography-tandem mass spectrometry (mu LC/MS/MS). The isolates selected for this analysis were from the sputum of a CF patient: strain 383 had a nonmucoid phenotype typical of isolates from the environment, and strain 2192, obtained from the same patient, had a mucoid phenotype typical of isolates from chronic CF lung infections, Strains 383 and 2192 were confirmed to be genetically identical by restriction endonuclease analysis, random amplified polymorphic DNA-PCR, and pulsed-field gel electrophoresis, Conditions of protein extraction were optimized for consistent high-resolution separation of several hundred proteins from these clinical isolates as detected by Coomassie staining of 2-D gels, Fourteen proteins were selected for analysis; this group included those whose expression was common between both strains as well as unique for each strain, The proteins were identified by mu LC/MS/MS of the peptides produced by an in-gel tryptic digestion and compared to translated data from the Pseudomonas Genome Project; optimization of this technique has allowed for the comparison of proteins expressed by strains 383 and 2192.
引用
收藏
页码:2495 / 2508
页数:14
相关论文
共 42 条
[1]  
[Anonymous], METHODS GEN MOL BACT
[2]   PSEUDOMONAS-AERUGINOSA OUTER-MEMBRANE PROTEIN OPRH - EXPRESSION FROM THE CLONED GENE AND FUNCTION IN EDTA AND GENTAMICIN RESISTANCE [J].
BELL, A ;
BAINS, M ;
HANCOCK, REW .
JOURNAL OF BACTERIOLOGY, 1991, 173 (21) :6657-6664
[3]   Mapping of Chlamydia trachomatis proteins by immobiline-polyacrylamide two-dimensional electrophoresis: Spot identification by N-terminal sequencing and immunoblotting [J].
Bini, L ;
SanchezCampillo, M ;
Santucci, A ;
Magi, B ;
Marzocchi, B ;
Comanducci, M ;
Christiansen, G ;
Birkelund, S ;
Cevenini, R ;
Vretou, E ;
Ratti, G ;
Pallini, V .
ELECTROPHORESIS, 1996, 17 (01) :185-190
[4]   CLONING AND CHARACTERIZATION OF THE KATB GENE OF PSEUDOMONAS-AERUGINOSA ENCODING A HYDROGEN PEROXIDE-INDUCIBLE CATALASE - PURIFICATION OF KATB, CELLULAR-LOCALIZATION, AND DEMONSTRATION THAT IT IS ESSENTIAL FOR OPTIMAL RESISTANCE TO HYDROGEN-PEROXIDE [J].
BROWN, SM ;
HOWELL, ML ;
VASIL, ML ;
ANDERSON, AJ ;
HASSETT, DJ .
JOURNAL OF BACTERIOLOGY, 1995, 177 (22) :6536-6544
[5]   NUCLEOTIDE-SEQUENCE AND EXPRESSION OF THE ALGE GENE INVOLVED IN ALGINATE BIOSYNTHESIS BY PSEUDOMONAS-AERUGINOSA [J].
CHU, L ;
MAY, TB ;
CHAKRABARTY, AM ;
MISRA, TK .
GENE, 1991, 107 (01) :1-10
[6]  
Cordwell SJ, 1999, ELECTROPHORESIS, V20, P3580, DOI 10.1002/(SICI)1522-2683(19991201)20:18<3580::AID-ELPS3580>3.0.CO
[7]  
2-2
[8]   Characterization of the serogroup O11O-antigen locus of Pseudomonas aeruginosa PA103 [J].
Dean, CR ;
Franklund, CV ;
Retief, JD ;
Coyne, MJ ;
Hatano, K ;
Evans, DJ ;
Pier, GB ;
Goldberg, JB .
JOURNAL OF BACTERIOLOGY, 1999, 181 (14) :4275-4284
[9]  
Elkins JG, 1999, APPL ENVIRON MICROB, V65, P4594
[10]   Specific lipopolysaccharide found in cystic fibrosis airway Pseudomonas aeruginosa [J].
Ernst, RK ;
Yi, EC ;
Guo, L ;
Lim, KB ;
Burns, JL ;
Hackett, M ;
Miller, SI .
SCIENCE, 1999, 286 (5444) :1561-1565