Proteomic comparison of membrane and extracellular proteins from invasive (PAO1) and cytotoxic (6206) strains of Pseudomonas aeruginosa

被引:1
作者
Nouwens, AS
Willcox, MDP
Walsh, BJ
Cordwell, SJ
机构
[1] Macquarie Univ, APAF, Sydney, NSW 2109, Australia
[2] Univ New S Wales, Cooperat Res Ctr Eye Res & Technol, Sydney, NSW 2052, Australia
关键词
extracellular protein; mass spectrometry; outer membrane protein; strain comparison; two-dimensional gel electrophoresis;
D O I
10.1002/1615-9861(200209)2:9<1325::AID-PROT1325>3.0.CO;2-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Strains of Pseudomonas aeruginosa can be phenotypically classified by their mode of pathogenicity as either invasive, where the bacterium is internalised by host cells, or cytotoxic, where the host cell is killed without internalisation through the expression of cytotoxicity factors. These phenotypes are thought to depend primarily on the interactions of pseudomonal membrane and secreted proteins with host cells. We report here comparisons of outer membrane and extracellular protein-enriched fractions from invasive (PAO1) and cytotoxic (6206) strains of P. aeruginosa separated by two-dimensional (2-D) gel electrophoresis. Gel image comparisons revealed the two strains express essentially identical membrane protein profiles under the conditions investigated. Membrane protein strain differences were typically the result of minor amino acid sequence variations resulting in small mass and isoelectric point shifts visible on 2-D gels. Analysis of extracellular proteins from stationary phase growth, however, revealed significantly different protein profiles. Extracellular fractions from the invasive PAO1 strain were dominated by extracellular proteases including elastase (LasB), LasA protease and chitin-binding protein, as well as several previously designated 'hypothetical' proteins. LasB appeared to be highly processed with 28 discrete mass and isoelectric point forms detected in this study. The significant number of active extracellular proteases (including LasB itself) may account for this processing. Conversely, extracellular fractions from strain 6206 consisted mainly of cellular and membrane exposed proteins including GroEL, DnaK and flagellar subunits. These are thought to result from cellular turnover during growth and the reliance on the secretory mechanisms of this strain to produce high levels of cytotoxicity factors, such as ExoU, which may be produced only upon specific interactions with host cells. These studies will aid in elucidating the differences between invasive and cytotoxic P. aeruginosa at the proteome level.
引用
收藏
页码:1325 / 1346
页数:22
相关论文
共 70 条
[61]  
TAN ASP, 1993, FEMS MICROBIOL LETT, V106, P281, DOI 10.1016/0378-1097(93)90416-Y
[62]   LASA AND LASB GENES OF PSEUDOMONAS-AERUGINOSA - ANALYSIS OF TRANSCRIPTION AND GENE-PRODUCT ACTIVITY [J].
TODER, DS ;
FERRELL, SJ ;
NEZEZON, JL ;
RUST, L ;
IGLEWSKI, BH .
INFECTION AND IMMUNITY, 1994, 62 (04) :1320-1327
[63]   High extracellular levels of Mycobacterium tuberculosis glutamine synthetase and superoxide dismutase in actively growing cultures are due to high expression and extracellular stability rather than to a protein-specific export mechanism [J].
Tullius, MV ;
Harth, G ;
Horwitz, MA .
INFECTION AND IMMUNITY, 2001, 69 (10) :6348-6363
[64]  
Vallis AJ, 1999, INFECT IMMUN, V67, P2040
[65]  
VanBogelen RA, 1999, ELECTROPHORESIS, V20, P2149, DOI 10.1002/(SICI)1522-2683(19990801)20:11<2149::AID-ELPS2149>3.0.CO
[66]  
2-N
[67]   DISTRIBUTION OF REPETITIVE DNA-SEQUENCES IN EUBACTERIA AND APPLICATION TO FINGERPRINTING OF BACTERIAL GENOMES [J].
VERSALOVIC, J ;
KOEUTH, T ;
LUPSKI, JR .
NUCLEIC ACIDS RESEARCH, 1991, 19 (24) :6823-6831
[68]  
Zhu H, 2000, CLIN EXP OPHTHALMOL, V28, P201
[69]  
Ziebandt AK, 2001, PROTEOMICS, V1, P480, DOI 10.1002/1615-9861(200104)1:4<480::AID-PROT480>3.0.CO
[70]  
2-O