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Antibiotic tolerance among clinical isolates of bacteria.

Elaine Tuomanen, +2 more
- 01 Oct 1986 - 
- Vol. 30, Iss: 4, pp 521-527
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TLDR
This work has characterized a novel type of pneumococcal mutant that grows in normal generation times and is as sensitive to growth inhibition by penicillin as the wild-type parent strain.
Abstract
One of the unique features of p-lactam antibiotics and other cell-wall inhibitors like vancomycin and bacitracin is that they can rapidly kill and in many cases lyse susceptible bacteria. Many other types of antibacterial agents (e.g., trimethoprim or chloramphenicol) are primarily bacteriostatic: they inhibit multiplication but do not cause an irreversible inactivation of the cell. In 1970 the characterization of a novel type of pneumococcal mutant was reported in the literature [1]. This mutant grows in normal generation times and is as sensitive to growth inhibition by penicillin as the wild-type parent strain. However, while cultures of the parent

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Citations
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Journal ArticleDOI

Mechanisms of biofilm resistance to antimicrobial agents

TL;DR: Owing to the heterogeneous nature of the biofilm, it is likely that there are multiple resistance mechanisms at work within a single community.
Journal ArticleDOI

Distinguishing between resistance, tolerance and persistence to antibiotic treatment.

TL;DR: This Opinion article describes recent studies of tolerance, resistance and persistence, outlining how a clear and distinct definition for each phenotype can be developed from these findings and proposes a framework for classifying the drug response of bacterial strains according to these definitions that is based on the measurement of the minimum inhibitory concentration.
Journal ArticleDOI

Clinical Relevance of Bacteriostatic versus Bactericidal Mechanisms of Action in the Treatment of Gram-Positive Bacterial Infections

TL;DR: Although bacteriostatic/bactericidal data may provide valuable information on the potential action of antibacterial agents in vitro, it is necessary to combine this information with pharmacokinetic and pharmacodynamic data to provide more meaningful prediction of efficacy in vivo.
Journal ArticleDOI

Targeting bacterial membrane function: an underexploited mechanism for treating persistent infections

TL;DR: Despite some drawbacks, membrane-active agents form an important new means of eradicating recalcitrant, non-growing bacteria.
Journal ArticleDOI

Antimicrobial resistance of Staphylococcus aureus: genetic basis.

B R Lyon, +1 more
TL;DR: This work has shown clear trends in the emergence of multiresislant S. aureus-related resistance as well as in the development of novel mechanisms for this resistance.
References
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Journal ArticleDOI

hipA, a newly recognized gene of Escherichia coli K-12 that affects frequency of persistence after inhibition of murein synthesis.

H S Moyed, +1 more
TL;DR: Transposons Tn5 and Tn10 have been inserted close to hipA making it possible to explore the molecular genetics of persistence, a long recognized but poorly understood phenomenon.
BookDOI

Microbial cell walls and membranes

TL;DR: Antibiotics inhibiting D-alanine metabolism in peptidoglycan biosynthesis: cycloserine, O-carbamoyl-D-serine, alaphosphin (L-alanyl-L-1-aminoethyl phosphonic acid) and the haloalanines .
Journal ArticleDOI

The rate of killing of Escherichia coli by beta-lactam antibiotics is strictly proportional to the rate of bacterial growth.

TL;DR: Slow growing bacteria became progressively more phenotypically tolerant to beta-lactam antibiotics as the generation time was extended, and all killing rates were a constant function of the bacterial generation time.
Journal ArticleDOI

Multiple Antibiotic Resistance in a Bacterium with Suppressed Autolytic System

TL;DR: Suppression of the activity of the cellular autolytic system of pneumococci causes simultaneous resistance against penicillin, D-cycloserine and phosphonomycin, a novel type of drug resistance mechanism in bacteria.
Journal ArticleDOI

Observations on the Mechanism of Action of Penicillin.

TL;DR: Penicillin acts either as a bacteriostatic or bactericidal agent depending on the experimental conditions and appears to be effective only when active multiplication takes place.
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