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Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis

The human microbiota harbors diverse bacterial and bacteriophage (phage) communities. Bacteria evolve to overcome phage infection, thereby driving phage evolution to counter bacterial resistance. Understanding how phages select for genetic alterations in medically relevant bacteria is important as p...

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Autores principales: Johnson, Cydney N., Palacios Araya, Dennise, Schink, Viviane, Islam, Moutusee, Mangalea, Mihnea R., Decurtis, Emily K., Ngo, Tuong‐Vi C., Palmer, Kelli L., Duerkop, Breck A.
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/PMC8924694/
https://www.ncbi.nlm.nih.gov/pubmed/35478284
http://dx.doi.org/10.1002/mbo3.1273
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author Johnson, Cydney N.
Palacios Araya, Dennise
Schink, Viviane
Islam, Moutusee
Mangalea, Mihnea R.
Decurtis, Emily K.
Ngo, Tuong‐Vi C.
Palmer, Kelli L.
Duerkop, Breck A.
author_facet Johnson, Cydney N.
Palacios Araya, Dennise
Schink, Viviane
Islam, Moutusee
Mangalea, Mihnea R.
Decurtis, Emily K.
Ngo, Tuong‐Vi C.
Palmer, Kelli L.
Duerkop, Breck A.
author_sort Johnson, Cydney N.
collection PubMed
description The human microbiota harbors diverse bacterial and bacteriophage (phage) communities. Bacteria evolve to overcome phage infection, thereby driving phage evolution to counter bacterial resistance. Understanding how phages select for genetic alterations in medically relevant bacteria is important as phages become established biologics for the treatment of multidrug‐resistant (MDR) bacterial infections. Before phages can be widely used as standalone or combination antibacterial therapies, we must obtain a deep understanding of the molecular mechanisms of phage infection and how host bacteria alter their genomes to become resistant. We performed coevolution experiments using a single Enterococcus faecalis strain and two distantly related phages to determine how phage pressure impacts the evolution of the E. faecalis genome. Whole‐genome sequencing of E. faecalis following continuous exposure to these two phages revealed mutations previously demonstrated to be essential for phage infection. We also identified mutations in genes previously unreported to be associated with phage infection in E. faecalis. Intriguingly, there was only one shared mutation in the E. faecalis genome that was selected by both phages tested, demonstrating that infection by two genetically distinct phages selects for diverse variants. This knowledge serves as the basis for the continued study of E. faecalis genome evolution during phage infection and can be used to inform the design of future therapeutics, such as phage cocktails, intended to target MDR E. faecalis.
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spelling pubmed-89246942022-03-21 Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis Johnson, Cydney N. Palacios Araya, Dennise Schink, Viviane Islam, Moutusee Mangalea, Mihnea R. Decurtis, Emily K. Ngo, Tuong‐Vi C. Palmer, Kelli L. Duerkop, Breck A. Microbiologyopen Original Articles The human microbiota harbors diverse bacterial and bacteriophage (phage) communities. Bacteria evolve to overcome phage infection, thereby driving phage evolution to counter bacterial resistance. Understanding how phages select for genetic alterations in medically relevant bacteria is important as phages become established biologics for the treatment of multidrug‐resistant (MDR) bacterial infections. Before phages can be widely used as standalone or combination antibacterial therapies, we must obtain a deep understanding of the molecular mechanisms of phage infection and how host bacteria alter their genomes to become resistant. We performed coevolution experiments using a single Enterococcus faecalis strain and two distantly related phages to determine how phage pressure impacts the evolution of the E. faecalis genome. Whole‐genome sequencing of E. faecalis following continuous exposure to these two phages revealed mutations previously demonstrated to be essential for phage infection. We also identified mutations in genes previously unreported to be associated with phage infection in E. faecalis. Intriguingly, there was only one shared mutation in the E. faecalis genome that was selected by both phages tested, demonstrating that infection by two genetically distinct phages selects for diverse variants. This knowledge serves as the basis for the continued study of E. faecalis genome evolution during phage infection and can be used to inform the design of future therapeutics, such as phage cocktails, intended to target MDR E. faecalis. John Wiley and Sons Inc. 2022-03-16 /pmc/articles/PMC8924694/ /pubmed/35478284 http://dx.doi.org/10.1002/mbo3.1273 Text en © 2022 The Authors. MicrobiologyOpen 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
Johnson, Cydney N.
Palacios Araya, Dennise
Schink, Viviane
Islam, Moutusee
Mangalea, Mihnea R.
Decurtis, Emily K.
Ngo, Tuong‐Vi C.
Palmer, Kelli L.
Duerkop, Breck A.
Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title_full Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title_fullStr Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title_full_unstemmed Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title_short Genetically distant bacteriophages select for unique genomic changes in Enterococcus faecalis
title_sort genetically distant bacteriophages select for unique genomic changes in enterococcus faecalis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924694/
https://www.ncbi.nlm.nih.gov/pubmed/35478284
http://dx.doi.org/10.1002/mbo3.1273
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