Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis

Abstract Biofilms are assemblages of sessile microorganisms that form an extracellular matrix around themselves and mediate attachment to surfaces. The major component of the extracellular matrix of Uropathogenic E. coli and other Enterobacteriaceae are curli fibers, making biofilms robust and resis...

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Main Authors: Bhawna Rathi, Surbhi Gupta, Parveen Kumar, Veerbhan Kesarwani, Rakesh Singh Dhanda, Sandeep Kumar Kushwaha, Manisha Yadav
Format: Article
Language:English
Published: Nature Portfolio 2022-11-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-23647-2
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author Bhawna Rathi
Surbhi Gupta
Parveen Kumar
Veerbhan Kesarwani
Rakesh Singh Dhanda
Sandeep Kumar Kushwaha
Manisha Yadav
author_facet Bhawna Rathi
Surbhi Gupta
Parveen Kumar
Veerbhan Kesarwani
Rakesh Singh Dhanda
Sandeep Kumar Kushwaha
Manisha Yadav
author_sort Bhawna Rathi
collection DOAJ
description Abstract Biofilms are assemblages of sessile microorganisms that form an extracellular matrix around themselves and mediate attachment to surfaces. The major component of the extracellular matrix of Uropathogenic E. coli and other Enterobacteriaceae are curli fibers, making biofilms robust and resistant to antimicrobials. It is therefore imperative to screen antibiofilm compounds that can impair biofilm formation. In the present study, we investigated the curli-dependent antibiofilm activity of caffeine against UPEC strain CFT073 and commensal strain E. coli K-12MG1655.Caffeine significantly reduced the biofilm formation of both UPEC and E. coli K-12 by 86.58% and 91.80% respectively at 48 mM caffeine as determined by Crystal Violet assay. These results were further confirmed by fluorescence microscopy and Scanning Electron Microscope (SEM). Caffeine significantly reduced the cytotoxicity and survivability of UPEC. Molecular docking analysis revealed a strong interaction between caffeine and curli regulator protein (Csg D) of E. coli. The qRT-PCR data also showed significant downregulation in the expression of CsgBA and the CsgDEFG operon at both 24 mM and 48 mM caffeine. The findings revealed that caffeine could inhibit E. coli biofilm formation by regulating curli assembly and thus may be used as an alternative therapeutic strategy for the treatment of chronic E. coli biofilm-related infections.
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spelling doaj.art-95d6001328f84548816a8cd27b33e0d32022-12-22T03:36:53ZengNature PortfolioScientific Reports2045-23222022-11-0112111310.1038/s41598-022-23647-2Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesisBhawna Rathi0Surbhi Gupta1Parveen Kumar2Veerbhan Kesarwani3Rakesh Singh Dhanda4Sandeep Kumar Kushwaha5Manisha Yadav6Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi (North Campus)Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi (North Campus)Department of Urology, University of Alabama at BirminghamHap BiosolutionsPvt. Ltd.Celluleris AB, VentureLabDBT-National Institute of Animal Biotechnology (NIAB)Dr. B. R. Ambedkar Center for Biomedical Research, University of Delhi (North Campus)Abstract Biofilms are assemblages of sessile microorganisms that form an extracellular matrix around themselves and mediate attachment to surfaces. The major component of the extracellular matrix of Uropathogenic E. coli and other Enterobacteriaceae are curli fibers, making biofilms robust and resistant to antimicrobials. It is therefore imperative to screen antibiofilm compounds that can impair biofilm formation. In the present study, we investigated the curli-dependent antibiofilm activity of caffeine against UPEC strain CFT073 and commensal strain E. coli K-12MG1655.Caffeine significantly reduced the biofilm formation of both UPEC and E. coli K-12 by 86.58% and 91.80% respectively at 48 mM caffeine as determined by Crystal Violet assay. These results were further confirmed by fluorescence microscopy and Scanning Electron Microscope (SEM). Caffeine significantly reduced the cytotoxicity and survivability of UPEC. Molecular docking analysis revealed a strong interaction between caffeine and curli regulator protein (Csg D) of E. coli. The qRT-PCR data also showed significant downregulation in the expression of CsgBA and the CsgDEFG operon at both 24 mM and 48 mM caffeine. The findings revealed that caffeine could inhibit E. coli biofilm formation by regulating curli assembly and thus may be used as an alternative therapeutic strategy for the treatment of chronic E. coli biofilm-related infections.https://doi.org/10.1038/s41598-022-23647-2
spellingShingle Bhawna Rathi
Surbhi Gupta
Parveen Kumar
Veerbhan Kesarwani
Rakesh Singh Dhanda
Sandeep Kumar Kushwaha
Manisha Yadav
Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
Scientific Reports
title Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
title_full Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
title_fullStr Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
title_full_unstemmed Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
title_short Anti-biofilm activity of caffeine against uropathogenic E. coli is mediated by curli biogenesis
title_sort anti biofilm activity of caffeine against uropathogenic e coli is mediated by curli biogenesis
url https://doi.org/10.1038/s41598-022-23647-2
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