Cargando…

CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection

Osteomyelitis, or bone infection, is often induced by antibiotic resistant Staphylococcus aureus strains of bacteria. Although debridement and long-term administration of antibiotics are the gold standard for osteomyelitis treatment, the increase in prevalence of antibiotic resistant bacterial strai...

Descripción completa

Detalles Bibliográficos
Autores principales: Cobb, Leah H., Park, JooYoun, Swanson, Elizabeth A., Beard, Mary Catherine, McCabe, Emily M., Rourke, Anna S., Seo, Keun Seok, Olivier, Alicia K., Priddy, Lauren B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874295/
https://www.ncbi.nlm.nih.gov/pubmed/31756187
http://dx.doi.org/10.1371/journal.pone.0220421
_version_ 1783472812392972288
author Cobb, Leah H.
Park, JooYoun
Swanson, Elizabeth A.
Beard, Mary Catherine
McCabe, Emily M.
Rourke, Anna S.
Seo, Keun Seok
Olivier, Alicia K.
Priddy, Lauren B.
author_facet Cobb, Leah H.
Park, JooYoun
Swanson, Elizabeth A.
Beard, Mary Catherine
McCabe, Emily M.
Rourke, Anna S.
Seo, Keun Seok
Olivier, Alicia K.
Priddy, Lauren B.
author_sort Cobb, Leah H.
collection PubMed
description Osteomyelitis, or bone infection, is often induced by antibiotic resistant Staphylococcus aureus strains of bacteria. Although debridement and long-term administration of antibiotics are the gold standard for osteomyelitis treatment, the increase in prevalence of antibiotic resistant bacterial strains limits the ability of clinicians to effectively treat infection. Bacteriophages (phages), viruses that in a lytic state can effectively kill bacteria, have gained recent attention for their high specificity, abundance in nature, and minimal risk of host toxicity. Previously, we have shown that CRISPR-Cas9 genomic editing techniques could be utilized to expand temperate bacteriophage host range and enhance bactericidal activity through modification of the tail fiber protein. In a dermal infection study, these CRISPR-Cas9 phages reduced bacterial load relative to unmodified phage. Thus we hypothesized this temperate bacteriophage, equipped with the CRISPR-Cas9 bactericidal machinery, would be effective at mitigating infection from a biofilm forming S. aureus strain in vitro and in vivo. In vitro, qualitative fluorescent imaging demonstrated superiority of phage to conventional vancomycin and fosfomycin antibiotics against S. aureus biofilm. Quantitative antibiofilm effects increased over time, at least partially, for all fosfomycin, phage, and fosfomycin-phage (dual) therapeutics delivered via alginate hydrogel. We developed an in vivo rat model of osteomyelitis and soft tissue infection that was reproducible and challenging and enabled longitudinal monitoring of infection progression. Using this model, phage (with and without fosfomycin) delivered via alginate hydrogel were successful in reducing soft tissue infection but not bone infection, based on bacteriological, histological, and scanning electron microscopy analyses. Notably, the efficacy of phage at mitigating soft tissue infection was equal to that of high dose fosfomycin. Future research may utilize this model as a platform for evaluation of therapeutic type and dose, and alternate delivery vehicles for osteomyelitis mitigation.
format Online
Article
Text
id pubmed-6874295
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-68742952019-12-06 CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection Cobb, Leah H. Park, JooYoun Swanson, Elizabeth A. Beard, Mary Catherine McCabe, Emily M. Rourke, Anna S. Seo, Keun Seok Olivier, Alicia K. Priddy, Lauren B. PLoS One Research Article Osteomyelitis, or bone infection, is often induced by antibiotic resistant Staphylococcus aureus strains of bacteria. Although debridement and long-term administration of antibiotics are the gold standard for osteomyelitis treatment, the increase in prevalence of antibiotic resistant bacterial strains limits the ability of clinicians to effectively treat infection. Bacteriophages (phages), viruses that in a lytic state can effectively kill bacteria, have gained recent attention for their high specificity, abundance in nature, and minimal risk of host toxicity. Previously, we have shown that CRISPR-Cas9 genomic editing techniques could be utilized to expand temperate bacteriophage host range and enhance bactericidal activity through modification of the tail fiber protein. In a dermal infection study, these CRISPR-Cas9 phages reduced bacterial load relative to unmodified phage. Thus we hypothesized this temperate bacteriophage, equipped with the CRISPR-Cas9 bactericidal machinery, would be effective at mitigating infection from a biofilm forming S. aureus strain in vitro and in vivo. In vitro, qualitative fluorescent imaging demonstrated superiority of phage to conventional vancomycin and fosfomycin antibiotics against S. aureus biofilm. Quantitative antibiofilm effects increased over time, at least partially, for all fosfomycin, phage, and fosfomycin-phage (dual) therapeutics delivered via alginate hydrogel. We developed an in vivo rat model of osteomyelitis and soft tissue infection that was reproducible and challenging and enabled longitudinal monitoring of infection progression. Using this model, phage (with and without fosfomycin) delivered via alginate hydrogel were successful in reducing soft tissue infection but not bone infection, based on bacteriological, histological, and scanning electron microscopy analyses. Notably, the efficacy of phage at mitigating soft tissue infection was equal to that of high dose fosfomycin. Future research may utilize this model as a platform for evaluation of therapeutic type and dose, and alternate delivery vehicles for osteomyelitis mitigation. Public Library of Science 2019-11-22 /pmc/articles/PMC6874295/ /pubmed/31756187 http://dx.doi.org/10.1371/journal.pone.0220421 Text en © 2019 Cobb et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cobb, Leah H.
Park, JooYoun
Swanson, Elizabeth A.
Beard, Mary Catherine
McCabe, Emily M.
Rourke, Anna S.
Seo, Keun Seok
Olivier, Alicia K.
Priddy, Lauren B.
CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title_full CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title_fullStr CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title_full_unstemmed CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title_short CRISPR-Cas9 modified bacteriophage for treatment of Staphylococcus aureus induced osteomyelitis and soft tissue infection
title_sort crispr-cas9 modified bacteriophage for treatment of staphylococcus aureus induced osteomyelitis and soft tissue infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6874295/
https://www.ncbi.nlm.nih.gov/pubmed/31756187
http://dx.doi.org/10.1371/journal.pone.0220421
work_keys_str_mv AT cobbleahh crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT parkjooyoun crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT swansonelizabetha crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT beardmarycatherine crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT mccabeemilym crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT rourkeannas crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT seokeunseok crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT olivieraliciak crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection
AT priddylaurenb crisprcas9modifiedbacteriophagefortreatmentofstaphylococcusaureusinducedosteomyelitisandsofttissueinfection