Hsp90 governs dispersion and drug resistance of fungal biofilms.

Fungal biofilms are a major cause of human mortality and are recalcitrant to most treatments due to intrinsic drug resistance. These complex communities of multiple cell types form on indwelling medical devices and their eradication often requires surgical removal of infected devices. Here we implic...

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Main Authors: Nicole Robbins, Priya Uppuluri, Jeniel Nett, Ranjith Rajendran, Gordon Ramage, Jose L Lopez-Ribot, David Andes, Leah E Cowen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-09-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3169563?pdf=render
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author Nicole Robbins
Priya Uppuluri
Jeniel Nett
Ranjith Rajendran
Gordon Ramage
Jose L Lopez-Ribot
David Andes
Leah E Cowen
author_facet Nicole Robbins
Priya Uppuluri
Jeniel Nett
Ranjith Rajendran
Gordon Ramage
Jose L Lopez-Ribot
David Andes
Leah E Cowen
author_sort Nicole Robbins
collection DOAJ
description Fungal biofilms are a major cause of human mortality and are recalcitrant to most treatments due to intrinsic drug resistance. These complex communities of multiple cell types form on indwelling medical devices and their eradication often requires surgical removal of infected devices. Here we implicate the molecular chaperone Hsp90 as a key regulator of biofilm dispersion and drug resistance. We previously established that in the leading human fungal pathogen, Candida albicans, Hsp90 enables the emergence and maintenance of drug resistance in planktonic conditions by stabilizing the protein phosphatase calcineurin and MAPK Mkc1. Hsp90 also regulates temperature-dependent C. albicans morphogenesis through repression of cAMP-PKA signalling. Here we demonstrate that genetic depletion of Hsp90 reduced C. albicans biofilm growth and maturation in vitro and impaired dispersal of biofilm cells. Further, compromising Hsp90 function in vitro abrogated resistance of C. albicans biofilms to the most widely deployed class of antifungal drugs, the azoles. Depletion of Hsp90 led to reduction of calcineurin and Mkc1 in planktonic but not biofilm conditions, suggesting that Hsp90 regulates drug resistance through different mechanisms in these distinct cellular states. Reduction of Hsp90 levels led to a marked decrease in matrix glucan levels, providing a compelling mechanism through which Hsp90 might regulate biofilm azole resistance. Impairment of Hsp90 function genetically or pharmacologically transformed fluconazole from ineffectual to highly effective in eradicating biofilms in a rat venous catheter infection model. Finally, inhibition of Hsp90 reduced resistance of biofilms of the most lethal mould, Aspergillus fumigatus, to the newest class of antifungals to reach the clinic, the echinocandins. Thus, we establish a novel mechanism regulating biofilm drug resistance and dispersion and that targeting Hsp90 provides a much-needed strategy for improving clinical outcome in the treatment of biofilm infections.
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spelling doaj.art-4e7ac91e2d9c4cd09ad8c363fde8739f2022-12-21T22:47:22ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-09-0179e100225710.1371/journal.ppat.1002257Hsp90 governs dispersion and drug resistance of fungal biofilms.Nicole RobbinsPriya UppuluriJeniel NettRanjith RajendranGordon RamageJose L Lopez-RibotDavid AndesLeah E CowenFungal biofilms are a major cause of human mortality and are recalcitrant to most treatments due to intrinsic drug resistance. These complex communities of multiple cell types form on indwelling medical devices and their eradication often requires surgical removal of infected devices. Here we implicate the molecular chaperone Hsp90 as a key regulator of biofilm dispersion and drug resistance. We previously established that in the leading human fungal pathogen, Candida albicans, Hsp90 enables the emergence and maintenance of drug resistance in planktonic conditions by stabilizing the protein phosphatase calcineurin and MAPK Mkc1. Hsp90 also regulates temperature-dependent C. albicans morphogenesis through repression of cAMP-PKA signalling. Here we demonstrate that genetic depletion of Hsp90 reduced C. albicans biofilm growth and maturation in vitro and impaired dispersal of biofilm cells. Further, compromising Hsp90 function in vitro abrogated resistance of C. albicans biofilms to the most widely deployed class of antifungal drugs, the azoles. Depletion of Hsp90 led to reduction of calcineurin and Mkc1 in planktonic but not biofilm conditions, suggesting that Hsp90 regulates drug resistance through different mechanisms in these distinct cellular states. Reduction of Hsp90 levels led to a marked decrease in matrix glucan levels, providing a compelling mechanism through which Hsp90 might regulate biofilm azole resistance. Impairment of Hsp90 function genetically or pharmacologically transformed fluconazole from ineffectual to highly effective in eradicating biofilms in a rat venous catheter infection model. Finally, inhibition of Hsp90 reduced resistance of biofilms of the most lethal mould, Aspergillus fumigatus, to the newest class of antifungals to reach the clinic, the echinocandins. Thus, we establish a novel mechanism regulating biofilm drug resistance and dispersion and that targeting Hsp90 provides a much-needed strategy for improving clinical outcome in the treatment of biofilm infections.http://europepmc.org/articles/PMC3169563?pdf=render
spellingShingle Nicole Robbins
Priya Uppuluri
Jeniel Nett
Ranjith Rajendran
Gordon Ramage
Jose L Lopez-Ribot
David Andes
Leah E Cowen
Hsp90 governs dispersion and drug resistance of fungal biofilms.
PLoS Pathogens
title Hsp90 governs dispersion and drug resistance of fungal biofilms.
title_full Hsp90 governs dispersion and drug resistance of fungal biofilms.
title_fullStr Hsp90 governs dispersion and drug resistance of fungal biofilms.
title_full_unstemmed Hsp90 governs dispersion and drug resistance of fungal biofilms.
title_short Hsp90 governs dispersion and drug resistance of fungal biofilms.
title_sort hsp90 governs dispersion and drug resistance of fungal biofilms
url http://europepmc.org/articles/PMC3169563?pdf=render
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