Effects of exogenous glucose on Pseudomonas aeruginosa biofilm formation and antibiotic resistance

被引:54
作者
She, Pengfei [1 ]
Wang, Yanle [1 ]
Liu, Yiqing [1 ]
Tan, Fang [1 ]
Chen, Lihua [1 ]
Luo, Zhen [1 ]
Wu, Yong [1 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Clin Lab, Changsha, Hunan, Peoples R China
关键词
antibiotic resistance; biofilm; extracellular polysaccharide; glucose; metabolomics; Pseudomonas aeruginosa; C-DI-GMP; CANDIDA-ALBICANS; GENE-EXPRESSION; EXOPOLYSACCHARIDE; MECHANISMS; PROTEINS; BACTERIA;
D O I
10.1002/mbo3.933
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pseudomonas aeruginosa is commonly found in nosocomial and life-threatening infections in patients. Biofilms formed by P. aeruginosa exhibit much greater resistance to antibiotics than the planktonic form of the bacteria. Few groups have studied the effects of glucose, a major carbon source, and metabolite, on P. aeruginosa biofilm formation and on its metabolic pathways. In this study, we investigated the effect of glucose on the biofilm formation ability of P. aeruginosa and carried out a metabolomic analysis to identify whether glucose alters the metabolic activity of P. aeruginosa in biofilms. We found that glucose efficiently promoted P. aeruginosa biofilm formation by upregulating the expression of the extracellular polysaccharide-related gene pslA. Treatment with glucose caused an increase in 7 metabolites (including 3-hydroxypropionic acid, glucose-6-phosphate, and 2,3-dimethylsuccinic acid) and a decrease in 18 metabolites (including myo-inositol, glutamine, and methoxamedrine) in the biofilm. In addition, there was a synergistic effect between glucose and horse serum on biofilm formation when the two were added in combination, which also increased the resistance of biofilm to levofloxacin therapy. Thus, our work sheds light on the underlying mechanisms by which glucose may enhance biofilm formation and identifies novel targets for developing strategies to counteract biofilm formation.
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页数:15
相关论文
共 47 条
[1]  
Santos APA, 2011, ARQ BRAS CARDIOL, V97, pE113
[2]   Hyperglycaemia and pulmonary infection [J].
Baker, Emma H. ;
Wood, David M. ;
Brennan, Amanda L. ;
Clark, Nicholas ;
Baines, Deborah L. ;
Philips, Barbara J. .
PROCEEDINGS OF THE NUTRITION SOCIETY, 2006, 65 (03) :227-235
[3]  
Bharati BK, 2013, CURR SCI INDIA, V105, P643
[4]   Genetic and biochemical analyses of the Pseudomonas aeruginosa Psl exopolysaccharide reveal overlapping roles for polysaccharide synthesis enzymes in Psl and LPS production [J].
Byrd, Matthew S. ;
Sadovskaya, Irina ;
Vinogradov, Evgueny ;
Lu, Haiping ;
Sprinkle, April B. ;
Richardson, Stephen H. ;
Ma, Luyan ;
Ralston, Brad ;
Parsek, Matthew R. ;
Anderson, Erin M. ;
Lam, Joseph S. ;
Wozniak, Daniel J. .
MOLECULAR MICROBIOLOGY, 2009, 73 (04) :622-638
[5]   Staining of extracellular polymeric substances and cells in bioaggregates [J].
Chen, Ming-Yuan ;
Lee, Duu-Jong ;
Tay, Joo-Hwa ;
Show, Kuan-Yeow .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 75 (02) :467-474
[6]  
Clinical and Laboratory Standards Institute (CLSI), 2015, M100S25 CLSI
[7]   BACTERIAL BIOFILMS IN NATURE AND DISEASE [J].
COSTERTON, JW ;
CHENG, KJ ;
GEESEY, GG ;
LADD, TI ;
NICKEL, JC ;
DASGUPTA, M ;
MARRIE, TJ .
ANNUAL REVIEW OF MICROBIOLOGY, 1987, 41 :435-464
[8]   A new family of mobilizable suicide plasmids based on broad host range R388 plasmid (IncW) and RP4 plasmid (IncPα) conjugative machineries and their cognate Escherichia coli host strains [J].
Demarre, G ;
Guérout, AM ;
Matsumoto-Mashimo, C ;
Rowe-Magnus, DA ;
Marlière, P ;
Mazel, D .
RESEARCH IN MICROBIOLOGY, 2005, 156 (02) :245-255
[9]   Biofilms: Microbial life on surfaces [J].
Donlan, RM .
EMERGING INFECTIOUS DISEASES, 2002, 8 (09) :881-890
[10]   A chemical proteomics approach to identify c-di-GMP binding proteins in Pseudomonas aeruginosa [J].
Duevel, Juliane ;
Bertinetti, Daniela ;
Moeller, Stefan ;
Schwede, Frank ;
Morr, Michael ;
Wissing, Josef ;
Radamm, Lena ;
Zimmermann, Bastian ;
Genieser, Hans-Gottfried ;
Jaensch, Lothar ;
Herberg, Friedrich W. ;
Haeussler, Susanne .
JOURNAL OF MICROBIOLOGICAL METHODS, 2012, 88 (02) :229-236