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Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease
Polymicrobial biofilms play an important role in the development and pathogenesis of CAUTI. Proteus mirabilis and Enterococcus faecalis are common CAUTI pathogens that persistently co-colonize the catheterized urinary tract and form biofilms with increased biomass and antibiotic resistance. In this...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055233/ https://www.ncbi.nlm.nih.gov/pubmed/36993593 http://dx.doi.org/10.1101/2023.03.17.533237 |
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author | Hunt, Benjamin C. Brix, Vitus Vath, Joseph Guterman, Beryl L. Taddei, Steven M. Learman, Brian S. Brauer, Aimee L. Shen, Shichen Qu, Jun Armbruster, Chelsie E. |
author_facet | Hunt, Benjamin C. Brix, Vitus Vath, Joseph Guterman, Beryl L. Taddei, Steven M. Learman, Brian S. Brauer, Aimee L. Shen, Shichen Qu, Jun Armbruster, Chelsie E. |
author_sort | Hunt, Benjamin C. |
collection | PubMed |
description | Polymicrobial biofilms play an important role in the development and pathogenesis of CAUTI. Proteus mirabilis and Enterococcus faecalis are common CAUTI pathogens that persistently co-colonize the catheterized urinary tract and form biofilms with increased biomass and antibiotic resistance. In this study, we uncover the metabolic interplay that drives biofilm enhancement and examine the contribution to CAUTI severity. Through compositional and proteomic biofilm analyses, we determined that the increase in biofilm biomass stems from an increase in the protein fraction of the polymicrobial biofilm matrix. We further observed an enrichment in proteins associated with ornithine and arginine metabolism in polymicrobial biofilms compared to single-species biofilms. We show that L-ornithine secretion by E. faecalis promotes arginine biosynthesis in P. mirabilis, and that disruption of this metabolic interplay abrogates the biofilm enhancement we see in vitro and leads to significant decreases in infection severity and dissemination in a murine CAUTI model. |
format | Online Article Text |
id | pubmed-10055233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100552332023-03-30 Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease Hunt, Benjamin C. Brix, Vitus Vath, Joseph Guterman, Beryl L. Taddei, Steven M. Learman, Brian S. Brauer, Aimee L. Shen, Shichen Qu, Jun Armbruster, Chelsie E. bioRxiv Article Polymicrobial biofilms play an important role in the development and pathogenesis of CAUTI. Proteus mirabilis and Enterococcus faecalis are common CAUTI pathogens that persistently co-colonize the catheterized urinary tract and form biofilms with increased biomass and antibiotic resistance. In this study, we uncover the metabolic interplay that drives biofilm enhancement and examine the contribution to CAUTI severity. Through compositional and proteomic biofilm analyses, we determined that the increase in biofilm biomass stems from an increase in the protein fraction of the polymicrobial biofilm matrix. We further observed an enrichment in proteins associated with ornithine and arginine metabolism in polymicrobial biofilms compared to single-species biofilms. We show that L-ornithine secretion by E. faecalis promotes arginine biosynthesis in P. mirabilis, and that disruption of this metabolic interplay abrogates the biofilm enhancement we see in vitro and leads to significant decreases in infection severity and dissemination in a murine CAUTI model. Cold Spring Harbor Laboratory 2023-04-24 /pmc/articles/PMC10055233/ /pubmed/36993593 http://dx.doi.org/10.1101/2023.03.17.533237 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Hunt, Benjamin C. Brix, Vitus Vath, Joseph Guterman, Beryl L. Taddei, Steven M. Learman, Brian S. Brauer, Aimee L. Shen, Shichen Qu, Jun Armbruster, Chelsie E. Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title | Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title_full | Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title_fullStr | Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title_full_unstemmed | Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title_short | Metabolic interplay between Proteus mirabilis and Enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
title_sort | metabolic interplay between proteus mirabilis and enterococcus faecalis facilitates polymicrobial biofilm formation and invasive disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055233/ https://www.ncbi.nlm.nih.gov/pubmed/36993593 http://dx.doi.org/10.1101/2023.03.17.533237 |
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