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Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa

Gram-negative bacterial pathogens have an outer membrane that restricts entry of molecules into the cell. Water-filled protein channels in the outer membrane, so-called porins, facilitate nutrient uptake and are thought to enable antibiotic entry. Here, we determined the role of porins in a major pa...

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Autores principales: Ude, Johanna, Tripathi, Vishwachi, Buyck, Julien M., Söderholm, Sandra, Cunrath, Olivier, Fanous, Joseph, Claudi, Beatrice, Egli, Adrian, Schleberger, Christian, Hiller, Sebastian, Bumann, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346889/
https://www.ncbi.nlm.nih.gov/pubmed/34326266
http://dx.doi.org/10.1073/pnas.2107644118
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author Ude, Johanna
Tripathi, Vishwachi
Buyck, Julien M.
Söderholm, Sandra
Cunrath, Olivier
Fanous, Joseph
Claudi, Beatrice
Egli, Adrian
Schleberger, Christian
Hiller, Sebastian
Bumann, Dirk
author_facet Ude, Johanna
Tripathi, Vishwachi
Buyck, Julien M.
Söderholm, Sandra
Cunrath, Olivier
Fanous, Joseph
Claudi, Beatrice
Egli, Adrian
Schleberger, Christian
Hiller, Sebastian
Bumann, Dirk
author_sort Ude, Johanna
collection PubMed
description Gram-negative bacterial pathogens have an outer membrane that restricts entry of molecules into the cell. Water-filled protein channels in the outer membrane, so-called porins, facilitate nutrient uptake and are thought to enable antibiotic entry. Here, we determined the role of porins in a major pathogen, Pseudomonas aeruginosa, by constructing a strain lacking all 40 identifiable porins and 15 strains carrying only a single unique type of porin and characterizing these strains with NMR metabolomics and antimicrobial susceptibility assays. In contrast to common assumptions, all porins were dispensable for Pseudomonas growth in rich medium and consumption of diverse hydrophilic nutrients. However, preferred nutrients with two or more carboxylate groups such as succinate and citrate permeated poorly in the absence of porins. Porins provided efficient translocation pathways for these nutrients with broad and overlapping substrate selectivity while efficiently excluding all tested antibiotics except carbapenems, which partially entered through OprD. Porin-independent permeation of antibiotics through the outer-membrane lipid bilayer was hampered by carboxylate groups, consistent with our nutrient data. Together, these results challenge common assumptions about the role of porins by demonstrating porin-independent permeation of the outer-membrane lipid bilayer as a major pathway for nutrient and drug entry into the bacterial cell.
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spelling pubmed-83468892021-08-23 Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa Ude, Johanna Tripathi, Vishwachi Buyck, Julien M. Söderholm, Sandra Cunrath, Olivier Fanous, Joseph Claudi, Beatrice Egli, Adrian Schleberger, Christian Hiller, Sebastian Bumann, Dirk Proc Natl Acad Sci U S A Biological Sciences Gram-negative bacterial pathogens have an outer membrane that restricts entry of molecules into the cell. Water-filled protein channels in the outer membrane, so-called porins, facilitate nutrient uptake and are thought to enable antibiotic entry. Here, we determined the role of porins in a major pathogen, Pseudomonas aeruginosa, by constructing a strain lacking all 40 identifiable porins and 15 strains carrying only a single unique type of porin and characterizing these strains with NMR metabolomics and antimicrobial susceptibility assays. In contrast to common assumptions, all porins were dispensable for Pseudomonas growth in rich medium and consumption of diverse hydrophilic nutrients. However, preferred nutrients with two or more carboxylate groups such as succinate and citrate permeated poorly in the absence of porins. Porins provided efficient translocation pathways for these nutrients with broad and overlapping substrate selectivity while efficiently excluding all tested antibiotics except carbapenems, which partially entered through OprD. Porin-independent permeation of antibiotics through the outer-membrane lipid bilayer was hampered by carboxylate groups, consistent with our nutrient data. Together, these results challenge common assumptions about the role of porins by demonstrating porin-independent permeation of the outer-membrane lipid bilayer as a major pathway for nutrient and drug entry into the bacterial cell. National Academy of Sciences 2021-08-03 2021-07-29 /pmc/articles/PMC8346889/ /pubmed/34326266 http://dx.doi.org/10.1073/pnas.2107644118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ude, Johanna
Tripathi, Vishwachi
Buyck, Julien M.
Söderholm, Sandra
Cunrath, Olivier
Fanous, Joseph
Claudi, Beatrice
Egli, Adrian
Schleberger, Christian
Hiller, Sebastian
Bumann, Dirk
Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title_full Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title_fullStr Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title_full_unstemmed Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title_short Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa
title_sort outer membrane permeability: antimicrobials and diverse nutrients bypass porins in pseudomonas aeruginosa
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346889/
https://www.ncbi.nlm.nih.gov/pubmed/34326266
http://dx.doi.org/10.1073/pnas.2107644118
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