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Author Notes:

vperrot@emory.edu

James Dickey: Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

Véronique Perrot: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

Karsten Becker, Editor

We thank A. Hanes for obtaining and donating the PYO phage cocktail, Robert Petit III for analyzing the sequencing data, Waqas Chaudhry for his expertise and consulting, Ingrid McCall for making the lab run smoothly, and Bruce Levin, kibbitzer-in-chief, for providing funding for and feedback on this study.

The authors have declared that no competing interests exist.

Subjects:

Research Funding:

This study was funded by NIH-NIGMS grant GM091875.

The Robert P. Apkarian Integrated Electron Microscopy Core is subsidized by the Emory College of Arts and Sciences and the Emory University School of Medicine and is one of the Emory Integrated Core Facilities, and the JEOL JEM-1400 120kV TEM is supported by NIH grant S10 RR025679.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Keywords:

  • phage therapy
  • antibiotic resistance
  • public health
  • bacterial biofilms
  • infection
  • experiment
  • case study
  • pretreatment
  • staphylococcus aureus

Adjunct phage treatment enhances the effectiveness of low antibiotic concentration against Staphylococcus aureus biofilms in vitro

Tools:

Journal Title:

PLoS ONE

Volume:

Volume 14, Number 1

Publisher:

, Pages e0209390-e0209390

Type of Work:

Article | Final Publisher PDF

Abstract:

Phage therapy is drawing more interest as antibiotic resistance becomes an ever more serious threat to public health. Bacterial biofilms represent a major obstacle in the fight against bacterial infections as they are inherently refractory to many types of antibiotics. Treating biofilms with phage has shown promise in a handful of experimental and case studies. However, quantification of the effect of phage combined with antibiotics is needed to pave the way for larger clinical trials. Here we explore the effect of using phage in combination with a total of nine antibiotics, applied simultaneously or as a pretreatment before antibiotics are applied to in vitro biofilms of Staphylococcus aureus. Most antibiotics alone were ineffective at low concentration (2×MIC), but the addition of phage to treatment regimens led to substantial improvements in efficacy. At high concentration (10×MIC), antibiotics alone were effective, and in most cases the addition of phage to treatment regimens did not improve efficacy. Using phage with rifampin was also very effective at reducing the outgrowth of resistant strains during the course of treatment.

Copyright information:

© 2019 Dickey, Perrot.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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