A simple solid media assay for detection of synergy between bacteriophages and antibiotics

Author:

Khong Ethan1,Oh Joseph J.1ORCID,Jimenez Julian M.2,Liu Roland1,Dunham Sage3ORCID,Monsibais Alisha3,Rhoads Alison1,Ghatbale Pooja1,Garcia Andrew1,Cobián Güemes Ana Georgina1ORCID,Blanc Alisha N.1,Chiu Megan1,Kuo Peiting1,Proost Marissa1,Kline Ahnika1,Aslam Saima4ORCID,Schooley Robert T.4,Whiteson Katrine3ORCID,Fraley Stephanie I.2,Pride David T.14ORCID

Affiliation:

1. Department of Pathology, University of California San Diego, La Jolla, California, USA

2. Department of Bioengineering, University of California San Diego, La Jolla, California, USA

3. Department of Molecular Biology and Biochemistry, University of California Irvine, Irvine, California, USA

4. Department of Medicine, University of California San Diego, La Jolla, California, USA

Abstract

ABSTRACT The emergence of antibiotic-resistant bacteria (ARB) has necessitated the development of alternative therapies to deal with this global threat. Bacteriophages (viruses that target bacteria) that kill ARB are one such alternative. Although phages have been used clinically for decades with inconsistent results, a number of recent advances in phage selection, propagation, and purification have enabled a reevaluation of their utility in contemporary clinical medicine. In most phage therapy cases, phages are administered in combination with antibiotics to ensure that patients receive the standard-of-care treatment. Some phages may work cooperatively with antibiotics to eradicate ARB, as often determined using non-standardized broth assays. We sought to develop a solid media-based assay to assess cooperativity between antibiotics and phages to offer a standardized platform for such testing. We modeled the interactions that occur between antibiotics and phages on solid medium to measure additive, antagonistic, and synergistic interactions. We then tested the method using different bacterial isolates and identified a number of isolates where synergistic interactions were identified. These interactions were not dependent on the specific organism, phage family, or antibiotic used. A priori susceptibility to the antibiotic or the specific phage were not requirements to observe synergistic interactions. Our data also confirm the potential for the restoration of vancomycin to treat vancomycin-resistant Enterococcus (VRE) when used in combination with phages. Solid media assays for the detection of cooperative interactions between antibiotics and phages can be an accessible technique adopted by clinical laboratories to evaluate antibiotic and phage choices in phage therapy. IMPORTANCE Bacteriophages have become an important alternative treatment for individuals with life-threatening antibiotic-resistant bacteria (ARB) infections. Because antibiotics represent the standard-of-care for treatment of ARB, antibiotics and phages often are delivered together without evidence that they work cooperatively. Testing for cooperativity can be difficult due to the equipment necessary and a lack of standardized means for performing the testing in liquid medium. We developed an assay using solid medium to identify interactions between antibiotics and phages for gram-positive and gram-negative bacteria. We modeled the interactions between antibiotics and phages on solid medium, and then tested multiple replicates of vancomycin-resistant Enterococcus (VRE) and Stenotrophomonas in the assay. For each organism, we identified synergy between different phage and antibiotic combinations. The development of this solid media assay for assessing synergy between phages and antibiotics will better inform the use of these combinations in the treatment of ARB infections.

Funder

Howard Hughes Medical Institute

HHS | National Institutes of Health

Publisher

American Society for Microbiology

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