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Antibiotic killing of drug-induced bacteriostatic cells
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Synopsis
Background
There is a long-standing belief that bacteriostatic drugs are inherently antagonistic to the action of bactericidal antibiotics. This belief is primarily due to the fact that the action of most bactericidal antibiotics requires the target bacteria to be growing. Since bacteriostatic drugs stop the growth of treated bacteria, these drugs would necessarily work against one another. We have recently shown that bacteria treated with high concentrations of bacteriostatic drugs retain some metabolic activity, dividing on average once per day.
Objectives
We seek to determine if this low level of growth is sufficient to allow for bactericidal antibiotics of different classes to still kill after bacteria are treated with bacteriostatic drugs.
Methods
We first treated
Escherichia coli
and
Staphylococcus aureus
with two different bacteriostatic drugs, followed by one of three bactericidal drugs of three different classes. The density of these bacteria was tracked over six days to determine the amount of killing that occurred.
Results
Our results question this long-standing belief by demonstrating conditions where sequential treatment with a bacteriostatic then bactericidal antibiotic is as or more effective than treatment with a bactericidal drug alone.
Conclusions
These results raise the need to investigate the pharmacodynamics of the joint action of bacteriostatic and bactericidal antibiotics
in vitro
and
in vivo
.
Title: Antibiotic killing of drug-induced bacteriostatic cells
Description:
Synopsis
Background
There is a long-standing belief that bacteriostatic drugs are inherently antagonistic to the action of bactericidal antibiotics.
This belief is primarily due to the fact that the action of most bactericidal antibiotics requires the target bacteria to be growing.
Since bacteriostatic drugs stop the growth of treated bacteria, these drugs would necessarily work against one another.
We have recently shown that bacteria treated with high concentrations of bacteriostatic drugs retain some metabolic activity, dividing on average once per day.
Objectives
We seek to determine if this low level of growth is sufficient to allow for bactericidal antibiotics of different classes to still kill after bacteria are treated with bacteriostatic drugs.
Methods
We first treated
Escherichia coli
and
Staphylococcus aureus
with two different bacteriostatic drugs, followed by one of three bactericidal drugs of three different classes.
The density of these bacteria was tracked over six days to determine the amount of killing that occurred.
Results
Our results question this long-standing belief by demonstrating conditions where sequential treatment with a bacteriostatic then bactericidal antibiotic is as or more effective than treatment with a bactericidal drug alone.
Conclusions
These results raise the need to investigate the pharmacodynamics of the joint action of bacteriostatic and bactericidal antibiotics
in vitro
and
in vivo
.
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