Literature DB >> 173706

Ultrastructural study of polymyxin-resistant isolates of Pseudomonas aeruginosa.

H E Gilleland, R G Murray.   

Abstract

Upon exposure to 6,000 U of polymyxin B sulfate per ml, cells of the polymyxin-sensitive PAO 1 strain of Pseudomonas aeruginosa displayed in thin sections long projections arising from the outer membrane of the cell wall and extensive cytoplasmic degradation with accumulation of cytoplasmic membrane infoldings. Polymyxin-resistant isolates derived from the PAO 1 strain, however, grew well in the presence of 6,000 U of polymyxin per ml and exhibited none of these effects, having instead the appearance of a typically healthy cell. Freeze-etching of cells of the sensitive strain grown in basal medium without polymyxin revealed a concave cell wall layer studded with numerous particles. Freeze-etching of cells of the resistant isolates grown in basal medium containing 6,000 U of polymyxin per ml revealed a concave cell wall layer (i.e., the outer half of the outer membrane) in which most of these particles were absent. Thus, acquisition of resistance to polymyxin was correlated with an alteration in the architecture of the outer membrane. When the resistant isolates were grown in the basal medium lacking polymyxin and then freeze-etched, the particle distribution in the concave cell wall layer resembled that of the sensitive parent strain. The cells had regained sensitivity to polymyxin upon suspension in medium containing 6,000 U/ml as determined by their failure to grow and by internal damages seen in thin sections. These cells also had acquired increased sensitivity to ethylenediaminetetraacetate, whereas the polymyxin-resistant cells grown in the presence of polymyxin were resistant to lysis by ethylenediaminetetraacetate. The polymyxin-resistant isolates were not stable mutants but instead represented an adaptive response to the presence of polymyxin in the medium.

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Year:  1976        PMID: 173706      PMCID: PMC233360          DOI: 10.1128/jb.125.1.267-281.1976

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  28 in total

1.  Low magnesium and phospholipid content of cell wals of Pseudomonas aeruginosa resistant to polymyxin.

Authors:  M R Brown; W M Watkins
Journal:  Nature       Date:  1970-09-26       Impact factor: 49.962

2.  Relation between cation and lipid content of cell walls of Pseudomonas aeruginosa, Proteus vulgaris and Klebsiella aerogenes and their sensitivity to polymyxin B and other antibacterial agents.

Authors:  M R Brown; S M Wood
Journal:  J Pharm Pharmacol       Date:  1972-03       Impact factor: 3.765

3.  Morphological and physiological investigations on the action of polymyxin B on Escherichia coli.

Authors:  K Wahn; G Lutsch; T Rockstroh; K Zapf
Journal:  Arch Mikrobiol       Date:  1968

4.  Electron microscopic studies on mode of action of polymyxin.

Authors:  M Koike; K Iida; T Matsuo
Journal:  J Bacteriol       Date:  1969-01       Impact factor: 3.490

5.  The nature of carbenicillin resistance in Pseudomonas aeruginosa.

Authors:  A H Thomas; R A Broadbridge
Journal:  J Gen Microbiol       Date:  1972-04

6.  Increase in sensitivity to antibiotics and lysozyme on deletion of lipopolysaccharides in Escherichia coli strains.

Authors:  S Tamaki; M Matsuhashi
Journal:  J Bacteriol       Date:  1973-04       Impact factor: 3.490

7.  Protein composition of the outer membrane of Salmonella typhimurium: effect of lipopolysaccharide mutations.

Authors:  G F Ames; E N Spudich; H Nikaido
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

8.  Interrelated effects of cold shock and osmotic pressure on the permeability of the Escherichia coli membrane to permease accumulated substrates.

Authors:  I G Leder
Journal:  J Bacteriol       Date:  1972-07       Impact factor: 3.490

9.  Alterations in the outer membrane of the cell envelope of heptose-deficient mutants of Escherichia coli.

Authors:  J Koplow; H Goldfine
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

10.  A three-dimensional molecular assembly model of a lipoprotein from the Escherichia coli outer membrane.

Authors:  M Inouye
Journal:  Proc Natl Acad Sci U S A       Date:  1974-06       Impact factor: 11.205

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  24 in total

1.  Outer membranes of gram-negative bacteria. XIX. Isolation from Pseudomonas aeruginosa PAO1 and use in reconstitution and definition of the permeability barrier.

Authors:  R E Hancock; H Nikaido
Journal:  J Bacteriol       Date:  1978-10       Impact factor: 3.490

2.  Decreased binding of polymyxin by polymyxin-resistant mutants of Salmonella typhimurium.

Authors:  M Vaara; T Vaara; M Sarvas
Journal:  J Bacteriol       Date:  1979-08       Impact factor: 3.490

3.  Chemical alterations in cell envelopes of polymyxin-resistant Pseudomonas aeruginosa isolates.

Authors:  H E Gilleland; R D Lyle
Journal:  J Bacteriol       Date:  1979-06       Impact factor: 3.490

4.  Adaptive acquisition of novobiocin resistance in Pasteurella multocida strains of avian origin.

Authors:  M Arif; F R Champlin
Journal:  Vet Res Commun       Date:  1998-11       Impact factor: 2.459

5.  The two-component system CprRS senses cationic peptides and triggers adaptive resistance in Pseudomonas aeruginosa independently of ParRS.

Authors:  Lucía Fernández; Håvard Jenssen; Manjeet Bains; Irith Wiegand; W James Gooderham; Robert E W Hancock
Journal:  Antimicrob Agents Chemother       Date:  2012-09-24       Impact factor: 5.191

6.  Gentamicin interaction with Pseudomonas aeruginosa cell envelope.

Authors:  N L Martin; T J Beveridge
Journal:  Antimicrob Agents Chemother       Date:  1986-06       Impact factor: 5.191

7.  Fatty acid alterations and polymyxin B binding by lipopolysaccharides from Pseudomonas aeruginosa adapted to polymyxin B resistance.

Authors:  R S Conrad; C Galanos
Journal:  Antimicrob Agents Chemother       Date:  1989-10       Impact factor: 5.191

8.  Use of a purified outer membrane protein F (porin) preparation of Pseudomonas aeruginosa as a protective vaccine in mice.

Authors:  H E Gilleland; M G Parker; J M Matthews; R D Berg
Journal:  Infect Immun       Date:  1984-04       Impact factor: 3.441

9.  Architecture of the outer membrane of Escherichia coli. III. Protein-lipopolysaccharide complexes in intramembraneous particles.

Authors:  L van Alphen; A Verkleij; J Leunissen-Bijvelt; B Lugtenberg
Journal:  J Bacteriol       Date:  1978-06       Impact factor: 3.490

10.  Comparison of the effects of mecillinam and 6-aminopenicillanic acid on Proteus mirabilis, Escherichia coli, and Staphylococcus aureus.

Authors:  V Lorian; B Atkinson
Journal:  Antimicrob Agents Chemother       Date:  1977-03       Impact factor: 5.191

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