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Surface action of gentamicin on Pseudomonas aeruginosa.

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TLDR
The morphological evidence suggests that the initial binding of the antibiotic disrupts the packing order of lipopolysaccharide of the outer membrane, which ultimately forms holes in the cell envelope and can lead to cell lysis, which makes aminoglycoside drugs particularly effective antibiotics.
Abstract
The mode of action of gentamicin has traditionally been considered to be at the 30S ribosomal level. However, the inhibition of bacterial protein synthesis alone appears to be insufficient to entirely explain the bactericidal effects. Bacteriolysis is also mediated through perturbation of the cell surface by gentamicin (J.L. Kadurugamuwa, J.S. Lam, and T.J. Beveridge, Antimicrob. Agents Chemother. 37:715-721, 1993). In order to separate the surface effect from protein synthesis in Pseudomonas aeruginosa PAO1, we chemically conjugated bovine serum albumin (BSA) to gentamicin, making the antibiotic too large to penetrate through the cell envelope to interact with the ribosomes of the cytoplasm. Furthermore, this BSA-gentamicin conjugate was also used to coat colloidal gold particles as a probe for electron microscopy to study the surface effect during antibiotic exposure. High-performance liquid chromatography confirmed the conjugation of the protein to the antibiotic. The conjugated gentamicin and BSA retained bactericidal activity and inhibited protein synthesis on isolated ribosomes in vitro but not on intact cells in vivo because of its exclusion from the cytoplasm. When reacted against the bacteria, numerous gentamicin-BSA-gold particles were clearly seen on the cell surfaces of whole mounts and thin sections of cells, while the cytoplasm was devoid of such particles. Disruption of the cell envelope was also observed since gentamicin-BSA and gentamicin-BSA-gold destabilized the outer membrane, evolved outer membrane blebs and vesicles, and formed holes in the cell surface. The morphological evidence suggests that the initial binding of the antibiotic disrupts the packing order of lipopolysaccharide of the outer membrane, which ultimately forms holes in the cell envelope and can lead to cell lysis. It is apparent that gentamicin has two potentially lethal effects on gram-negative cells, that resulting from inhibition of protein synthesis and that resulting from surface perturbation; the two effects in concert make aminoglycoside drugs particularly effective antibiotics. Images

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Membrane vesicles traffic signals and facilitate group activities in a prokaryote

TL;DR: It is shown that the opportunistic human pathogen Pseudomonas aeruginosa packages the signalling molecule 2-heptyl-3-hydroxy-4-quinolone into membrane vesicles that serve to traffic this molecule within a population, illustrating that a prokaryote possesses a signal trafficking system with features common to those used by higher organisms.
Journal ArticleDOI

Virulence factors are released from Pseudomonas aeruginosa in association with membrane vesicles during normal growth and exposure to gentamicin: a novel mechanism of enzyme secretion.

TL;DR: Both types of vesicles contained DNA, with a significantly higher content in g-MVs, and could play an important role in genetic transformation and disease by serving as a transport vehicle for DNA and virulence factors and are presumably involved in septic shock.
Journal ArticleDOI

Types and origins of bacterial membrane vesicles.

TL;DR: An overview of the structures and compositions of the various vesicle types are provided, including classic outer-membrane vesicles and newly identified types that are induced by phage-derived autolysins.
Journal ArticleDOI

Small Molecule-Capped Gold Nanoparticles as Potent Antibacterial Agents That Target Gram-Negative Bacteria

TL;DR: A new strategy in designing antibacterial agents is illustrated--a series of commercially available compounds, amino-substituted pyrimidines, when presented on gold nanoparticles (NPs), show antibacterial activities against multidrug-resistant clinical isolates, without external sources of energy such as IR.
Journal ArticleDOI

Membrane Vesicles: an Overlooked Component of the Matrices of Biofilms

TL;DR: It is shown that membrane vesicles (MVs), structures derived from the outer membrane of gram-negative bacteria, are a common particulate feature of the matrix of Pseudomonas aeruginosa biofilms and were established as common biofilm constituents.
References
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Journal ArticleDOI

Controlled nucleation for the regulation of the particle size in monodisperse gold suspensions

G. Frens
- 01 Jan 1973 - 
TL;DR: In this article, a series of monodisperse suspensions of the same chemical composition but of rather different particle sizes was used to study particle size dependent phenomena, such as Brownian motion, light scattering, sedimentation and electrophoresis of small particles.
Journal ArticleDOI

Agents that increase the permeability of the outer membrane.

TL;DR: Chelators (such as EDTA, nitrilotriacetic acid, and sodium hexametaphosphate), which disintegrate the outer membrane by removing Mg2+ and Ca2+, are effective and valuable permeabilizers.
Journal ArticleDOI

Ultrastructural localization of intracellular antigens by the use of protein A-gold complex.

TL;DR: An immunocytochemical technique for the demonstration of intracellular antigens (secretory proteins) on thin sections is reported and the protein A-gold technique is proposed as a general method for visualization of antigenic sites onthin sections.
Journal ArticleDOI

Bacterial uptake of aminoglycoside antibiotics.

TL;DR: A critical overview of the process of aminoglycoside uptake is presented and a number of unresolved issues about the overall process are addressed to suggest directions for future research.
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