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Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages

Brevibacillus laterosporus is often present in beehives, including presence in hives infected with the causative agent of American Foulbrood (AFB), Paenibacillus larvae. In this work, 12 B. laterosporus bacteriophages induced bactericidal products in their host. Results demonstrate that P. larvae is...

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Autores principales: Brady, T. Scott, Fajardo, Christopher P., Merrill, Bryan D., Hilton, Jared A., Graves, Kiel A., Eggett, Dennis L., Hope, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315864/
https://www.ncbi.nlm.nih.gov/pubmed/30518109
http://dx.doi.org/10.3390/antibiotics7040105
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author Brady, T. Scott
Fajardo, Christopher P.
Merrill, Bryan D.
Hilton, Jared A.
Graves, Kiel A.
Eggett, Dennis L.
Hope, Sandra
author_facet Brady, T. Scott
Fajardo, Christopher P.
Merrill, Bryan D.
Hilton, Jared A.
Graves, Kiel A.
Eggett, Dennis L.
Hope, Sandra
author_sort Brady, T. Scott
collection PubMed
description Brevibacillus laterosporus is often present in beehives, including presence in hives infected with the causative agent of American Foulbrood (AFB), Paenibacillus larvae. In this work, 12 B. laterosporus bacteriophages induced bactericidal products in their host. Results demonstrate that P. larvae is susceptible to antimicrobials induced from field isolates of the bystander, B. laterosporus. Bystander antimicrobial activity was specific against the pathogen and not other bacterial species, indicating that the production was likely due to natural competition between the two bacteria. Three B. laterosporus phages were combined in a cocktail to treat AFB. Healthy hives treated with B. laterosporus phages experienced no difference in brood generation compared to control hives over 8 weeks. Phage presence in bee larvae after treatment rose to 60.8 ± 3.6% and dropped to 0 ± 0.8% after 72 h. In infected hives the recovery rate was 75% when treated, however AFB spores were not susceptible to the antimicrobials as evidenced by recurrence of AFB. We posit that the effectiveness of this treatment is due to the production of the bactericidal products of B. laterosporus when infected with phages resulting in bystander-killing of P. larvae. Bystander phage therapy may provide a new avenue for antibacterial production and treatment of disease.
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spelling pubmed-63158642019-01-11 Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages Brady, T. Scott Fajardo, Christopher P. Merrill, Bryan D. Hilton, Jared A. Graves, Kiel A. Eggett, Dennis L. Hope, Sandra Antibiotics (Basel) Article Brevibacillus laterosporus is often present in beehives, including presence in hives infected with the causative agent of American Foulbrood (AFB), Paenibacillus larvae. In this work, 12 B. laterosporus bacteriophages induced bactericidal products in their host. Results demonstrate that P. larvae is susceptible to antimicrobials induced from field isolates of the bystander, B. laterosporus. Bystander antimicrobial activity was specific against the pathogen and not other bacterial species, indicating that the production was likely due to natural competition between the two bacteria. Three B. laterosporus phages were combined in a cocktail to treat AFB. Healthy hives treated with B. laterosporus phages experienced no difference in brood generation compared to control hives over 8 weeks. Phage presence in bee larvae after treatment rose to 60.8 ± 3.6% and dropped to 0 ± 0.8% after 72 h. In infected hives the recovery rate was 75% when treated, however AFB spores were not susceptible to the antimicrobials as evidenced by recurrence of AFB. We posit that the effectiveness of this treatment is due to the production of the bactericidal products of B. laterosporus when infected with phages resulting in bystander-killing of P. larvae. Bystander phage therapy may provide a new avenue for antibacterial production and treatment of disease. MDPI 2018-12-04 /pmc/articles/PMC6315864/ /pubmed/30518109 http://dx.doi.org/10.3390/antibiotics7040105 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brady, T. Scott
Fajardo, Christopher P.
Merrill, Bryan D.
Hilton, Jared A.
Graves, Kiel A.
Eggett, Dennis L.
Hope, Sandra
Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title_full Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title_fullStr Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title_full_unstemmed Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title_short Bystander Phage Therapy: Inducing Host-Associated Bacteria to Produce Antimicrobial Toxins against the Pathogen Using Phages
title_sort bystander phage therapy: inducing host-associated bacteria to produce antimicrobial toxins against the pathogen using phages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315864/
https://www.ncbi.nlm.nih.gov/pubmed/30518109
http://dx.doi.org/10.3390/antibiotics7040105
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