absence of membrane phosphatidylcholine does not affect virulence and stress tolerance phenotypes in the opportunistic pathogen pseudomonas aeruginosa没有膜磷脂酰胆碱不影响毒性和抗压力机会病原体铜绿假单胞菌的表型.pdfVIP
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absence of membrane phosphatidylcholine does not affect virulence and stress tolerance phenotypes in the opportunistic pathogen pseudomonas aeruginosa没有膜磷脂酰胆碱不影响毒性和抗压力机会病原体铜绿假单胞菌的表型
Absence of Membrane Phosphatidylcholine Does Not
Affect Virulence and Stress Tolerance Phenotypes in the
Opportunistic Pathogen Pseudomonas aeruginosa
1 2 1
Adel A. Malek , Matthew J. Wargo , Deborah A. Hogan *
1 Department of Microbiology and Immunology, Dartmouth Medical School, Hanover, New Hampshire, United States of America, 2 Department of Microbiology and
Molecular Genetics, University of Vermont College of Medicine, Burlington, Vermont, United States of America
Abstract
During growth in presence of choline, both laboratory and clinical Pseudomonas aeruginosa strains synthesize
phosphatidylcholine (PC), and PC makes up ,4% of the total membrane phospholipid content. In all the strains tested,
PC synthesis occurred only when choline is provided exogenously. Mutants defective in synthesis of PC were generated in
the strain backgrounds PAO1 and PA14. Minimum inhibitory concentration studies testing sensitivity of PC-deficient strains
towards various antibiotics and cationic antimicrobial peptides revealed no differences as compared to wild-type strains.
Mutants incapable of synthesizing PC were also found to be unaffected in motility and biofilm formation on abiotic surfaces,
colonization of biotic surfaces and virulence in a mouse infection model. A global phenotypic microarray was further used
to identify conditions wherein membrane PC may play a role of in P. aeruginosa. No culture conditions were identified
wherein wild-type and PC-deficient mutants showed phenotypic differences. Membrane PC may serve a highly specific role
during P. aeruginosa interactions with its eukaryotic hosts based on all the clinical strains tested retaining the ability to
synthesize it during availability of choline.
Citation: Ma
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