Impact of the biofilm mode of growth on the inner membrane phospholipid composition and lipid domains in Pseudomonas aeruginosa

被引:58
作者
Benamara, Hayette [1 ]
Rihouey, Christophe [1 ]
Jouenne, Thierry [1 ]
Alexandre, Stephane [1 ]
机构
[1] Univ Rouen, Prote Platform IFRMP23, CNRS, PBS Lab,UMR 6270,FR 3038, F-76821 Mont St Aignan, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2011年 / 1808卷 / 01期
关键词
Biofilm; Pseudomonas aeruginosa; Lipidome; Inner membrane; Monolayer; Mass spectroscopy; ESCHERICHIA-COLI BIOFILMS; ANTIBIOTIC-RESISTANCE; GENE-EXPRESSION; BACTERIAL BIOFILMS; PROTEOMIC ANALYSIS; OUTER-MEMBRANE; FATTY; ADHESION; CELLS; BIOSYNTHESIS;
D O I
10.1016/j.bbamem.2010.09.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many studies using genetic and proteomic approaches have revealed phenotypic differences between planktonic and sessile bacteria but the mechanisms of biofilm formation and the switch between the two growth modes are not well understood yet. In this study, we focused on inner membrane lipidome modifications when Pseudomonas aeruginosa cells were grown as biofilm. Lipid analyses were performed by Electrospray Ionization Mass Spectrometry. Results showed a drastic decrease of the uneven-numbered chain phospholipids and a slight increase of long chain PEs in sessile organisms as compared with planktonic counterparts, suggesting a better lipid stability in the bilayer and a decrease in membrane fluidity. The impact of sessile growth on lipid domains was then investigated by Brewster Angle Microscopy (BAM) and Atomic Force Microscopy (AFM). Observations showed that inner membrane lipids of P. aeruginosa formed domains when the pressure was close to physiological conditions and that these domains were larger for lipids extracted from biofilm bacteria. This is coherent with the mass spectrometry analyses. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 55 条
[1]  
Albelo ST, 1997, FEMS MICROBIOL LETT, V156, P271, DOI 10.1016/S0378-1097(97)00440-0
[2]   Bacterially speaking [J].
Bassler, BL ;
Losick, R .
CELL, 2006, 125 (02) :237-246
[3]   A Pseudomonas putida cardiolipin synthesis mutant exhibits increased sensitivity to drugs related to transport functionality [J].
Bernal, Patricia ;
Munoz-Rojas, Jesus ;
Hurtado, Ana ;
Ramos, Juan L. ;
Segura, Ana .
ENVIRONMENTAL MICROBIOLOGY, 2007, 9 (05) :1135-1145
[4]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[5]   An improved method for rapid generation of unmarked Pseudomonas aeruginosa deletion mutants -: art. no. 30 [J].
Choi, KH ;
Schweizer, HP .
BMC MICROBIOLOGY, 2005, 5 (1)
[6]   Lipid domains of mycobacteria studied with fluorescent molecular probes [J].
Christensen, H ;
Garton, NJ ;
Horobin, RW ;
Minnikin, DE ;
Barer, MR .
MOLECULAR MICROBIOLOGY, 1999, 31 (05) :1561-1572
[7]   Immobilization induces alterations in the outer membrane protein pattern of Yersinia ruckeri [J].
Coquet, L ;
Cosette, P ;
Dé, E ;
Galas, L ;
Vaudry, H ;
Rihouey, C ;
Lerouge, P ;
Junter, GA ;
Jouenne, T .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (06) :1988-1998
[8]   Bacterial biofilms: A common cause of persistent infections [J].
Costerton, JW ;
Stewart, PS ;
Greenberg, EP .
SCIENCE, 1999, 284 (5418) :1318-1322
[9]   Effect of selected environmental and physico-chemical factors on bacterial cytoplasmic membranes [J].
Denich, TJ ;
Beaudette, LA ;
Lee, H ;
Trevors, JT .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 52 (02) :149-182
[10]   The impact of membrane lipid composition on antimicrobial function of an α-helical peptide [J].
Dennison, Sarah R. ;
Morton, Leslie H. G. ;
Harris, Frederick ;
Phoenix, David A. .
CHEMISTRY AND PHYSICS OF LIPIDS, 2008, 151 (02) :92-102