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Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages

The evolution and spread of antibiotic‐resistant bacteria have renewed interest in phage therapy, the use of bacterial viruses (phages) to combat bacterial infections. The delivery of phages in cocktails where constituent phages target different modalities (e.g., receptors) may improve treatment out...

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Autores principales: Borin, Joshua M., Lee, Justin J., Gerbino, Krista R., Meyer, Justin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850009/
https://www.ncbi.nlm.nih.gov/pubmed/36699129
http://dx.doi.org/10.1111/eva.13518
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author Borin, Joshua M.
Lee, Justin J.
Gerbino, Krista R.
Meyer, Justin R.
author_facet Borin, Joshua M.
Lee, Justin J.
Gerbino, Krista R.
Meyer, Justin R.
author_sort Borin, Joshua M.
collection PubMed
description The evolution and spread of antibiotic‐resistant bacteria have renewed interest in phage therapy, the use of bacterial viruses (phages) to combat bacterial infections. The delivery of phages in cocktails where constituent phages target different modalities (e.g., receptors) may improve treatment outcomes by making it more difficult for bacteria to evolve resistance. However, the multipartite nature of cocktails may lead to unintended evolutionary and ecological outcomes. Here, we compare a 2‐phage cocktail with a largely unconsidered group of phages: generalists that can infect through multiple, independent receptors. We find that λ phage generalists and cocktails that target the same receptors (LamB and OmpF) suppress Escherichia coli similarly for ~2 days. Yet, a “trained” generalist phage, which previously adapted to its host via 28 days of coevolution, demonstrated superior suppression. To understand why the trained generalist was more effective, we measured the resistance of bacteria against each of our phages. We find that, when bacteria were assailed by two phages in the cocktail, they evolved mutations in manXYZ, a host inner‐membrane transporter that λ uses to move its DNA across the periplasmic space and into the cell for infection. This provided cross‐resistance against the cocktail and untrained generalist. However, these mutations were ineffective at blocking the trained generalist because, through coevolutionary training, it evolved to bypass manXYZ resistance. The trained generalist's past experiences in training make it exceedingly difficult for bacteria to evolve resistance, further demonstrating the utility of coevolutionary phage training for improving the therapeutic properties of phages.
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spelling pubmed-98500092023-01-24 Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages Borin, Joshua M. Lee, Justin J. Gerbino, Krista R. Meyer, Justin R. Evol Appl Original Articles The evolution and spread of antibiotic‐resistant bacteria have renewed interest in phage therapy, the use of bacterial viruses (phages) to combat bacterial infections. The delivery of phages in cocktails where constituent phages target different modalities (e.g., receptors) may improve treatment outcomes by making it more difficult for bacteria to evolve resistance. However, the multipartite nature of cocktails may lead to unintended evolutionary and ecological outcomes. Here, we compare a 2‐phage cocktail with a largely unconsidered group of phages: generalists that can infect through multiple, independent receptors. We find that λ phage generalists and cocktails that target the same receptors (LamB and OmpF) suppress Escherichia coli similarly for ~2 days. Yet, a “trained” generalist phage, which previously adapted to its host via 28 days of coevolution, demonstrated superior suppression. To understand why the trained generalist was more effective, we measured the resistance of bacteria against each of our phages. We find that, when bacteria were assailed by two phages in the cocktail, they evolved mutations in manXYZ, a host inner‐membrane transporter that λ uses to move its DNA across the periplasmic space and into the cell for infection. This provided cross‐resistance against the cocktail and untrained generalist. However, these mutations were ineffective at blocking the trained generalist because, through coevolutionary training, it evolved to bypass manXYZ resistance. The trained generalist's past experiences in training make it exceedingly difficult for bacteria to evolve resistance, further demonstrating the utility of coevolutionary phage training for improving the therapeutic properties of phages. John Wiley and Sons Inc. 2022-12-09 /pmc/articles/PMC9850009/ /pubmed/36699129 http://dx.doi.org/10.1111/eva.13518 Text en © 2022 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Borin, Joshua M.
Lee, Justin J.
Gerbino, Krista R.
Meyer, Justin R.
Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title_full Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title_fullStr Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title_full_unstemmed Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title_short Comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
title_sort comparison of bacterial suppression by phage cocktails, dual‐receptor generalists, and coevolutionarily trained phages
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850009/
https://www.ncbi.nlm.nih.gov/pubmed/36699129
http://dx.doi.org/10.1111/eva.13518
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