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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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