Javascript must be enabled to continue!
Antibiotic killing of drug-induced bacteriostatic cells
View through CrossRef
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
.
Related Results
Selection of Injectable Drug Product Composition using Machine Learning Models (Preprint)
Selection of Injectable Drug Product Composition using Machine Learning Models (Preprint)
BACKGROUND
As of July 2020, a Web of Science search of “machine learning (ML)” nested within the search of “pharmacokinetics or pharmacodynamics” yielded over 100...
Association between Awareness on Antibiotic Resistance and Antibiotic Misuse Among Saudi University Students
Association between Awareness on Antibiotic Resistance and Antibiotic Misuse Among Saudi University Students
Background:
Saudi Arabia has the highest prevalence of resistant pathogens in the Gulf Region, with a rapid increase in antibiotic resistance seen in recent years. ...
NK-92 Preferentially Targets Acute Myeloid Leukemia Stem Cells
NK-92 Preferentially Targets Acute Myeloid Leukemia Stem Cells
Abstract
Abstract 4300
Introduction:
Outcome of patients with acute myeloid leukemia (AML) remains poor because m...
Successful transfection of Lymphoblastoid cell line (Preprint)
Successful transfection of Lymphoblastoid cell line (Preprint)
BACKGROUND
Immortalization is the stage that the cell goes through before full transformation [1]. Human resting B lymphocytes from peripheral blood are eas...
Abstract CT053: Use of CRISPR knock-out screen to identify genes that regulate tumor cell sensitivity to NK cell-based immunotherapy
Abstract CT053: Use of CRISPR knock-out screen to identify genes that regulate tumor cell sensitivity to NK cell-based immunotherapy
Abstract
Natural killer (NK) cells play a key role in tumor immune surveillance by their ability to recognize and kill both hematological and solid tumor cells. NK c...
Abstract PR03: Use of CRISPR knockout screen to identify genes that regulate tumor cell sensitivity to NK cell-based immunotherapy
Abstract PR03: Use of CRISPR knockout screen to identify genes that regulate tumor cell sensitivity to NK cell-based immunotherapy
Abstract
Natural killer (NK) cells play a key role in tumor immune surveillance by their ability to recognize and kill both hematologic and solid tumor cells. NK cel...
P54 Enhancing antibiotic efficacy through nanotechnology: innovations in targeted antimicrobial delivery
P54 Enhancing antibiotic efficacy through nanotechnology: innovations in targeted antimicrobial delivery
Abstract
Background
Antibiotic resistance poses a growing global health threat, demanding innovative solutions to enhance treatm...
Evolution of Antimicrobial Resistance in Community vs. Hospital-Acquired Infections
Evolution of Antimicrobial Resistance in Community vs. Hospital-Acquired Infections
Abstract
Introduction
Hospitals are high-risk environments for infections. Despite the global recognition of these pathogens, few studies compare microorganisms from community-acqu...

