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JoVE Journal
Immunology and Infection
Une plaque de microtitrage à 96 puits à base Méthode de formation suivi et les tests de sensibili...
Une plaque de microtitrage à 96 puits à base Méthode de formation suivi et les tests de sensibili...
JoVE Journal
Immunology and Infection
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JoVE Journal Immunology and Infection
A 96 Well Microtiter Plate-based Method for Monitoring Formation and Antifungal Susceptibility Testing of Candida albicans Biofilms

Une plaque de microtitrage à 96 puits à base Méthode de formation suivi et les tests de sensibilité antifongique des Candida albicans Les biofilms

Full Text
46,554 Views
07:19 min
October 21, 2010

DOI: 10.3791/2287-v

Christopher G. Pierce1,2, Priya Uppuluri1,2, Sushma Tummala1,2, Jose L. Lopez-Ribot1,2

1Department of Biology,University of Texas San Antonio - UTSA, 2South Texas Center for Emerging Infectious Diseases,University of Texas San Antonio - UTSA

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This article presents a straightforward and efficient method for forming Candida albicans biofilms using 96 well microtiter plates. The method is particularly useful for assessing antifungal susceptibility in biofilm cells.

Key Study Components

Area of Science

  • Microbiology
  • Mycology
  • Antifungal susceptibility testing

Background

  • Candida albicans is a common fungal pathogen.
  • Biofilms pose significant challenges in treating fungal infections.
  • Understanding antifungal susceptibility in biofilms is crucial for effective treatment.
  • Traditional methods may not accurately reflect biofilm behavior.

Purpose of Study

  • To develop a rapid method for biofilm formation.
  • To evaluate the effectiveness of antifungal agents against biofilms.
  • To establish a reproducible testing protocol using microtiter plates.

Methods Used

  • Formation of Candida albicans biofilms in 96 well microtiter plates.
  • Incubation of biofilms with antifungal agents for 24 to 48 hours.
  • Use of a colorimetric method to assess metabolic activity.
  • Determination of minimum inhibitory concentration (MIC) for antifungals.

Main Results

  • Successful formation of Candida albicans biofilms was achieved.
  • The method demonstrated high reproducibility and ease of use.
  • Antifungal susceptibility testing provided clear results.
  • The approach is cost-effective and allows for multiple samples.

Conclusions

  • This method is a valuable tool for studying Candida albicans biofilms.
  • It facilitates the assessment of antifungal susceptibility.
  • The technique can enhance research in fungal pathogenesis and treatment.

Frequently Asked Questions

What is the significance of studying Candida albicans biofilms?
Studying biofilms is crucial as they are associated with increased resistance to antifungal treatments.
How does the colorimetric method work?
The colorimetric method measures metabolic activity, indicating the viability of cells within the biofilm.
What are the advantages of using microtiter plates?
Microtiter plates allow for high-throughput screening and are cost-effective for large sample sizes.
Can this method be applied to other fungal species?
While this study focuses on Candida albicans, the method may be adaptable to other fungi.
What is the typical incubation time for antifungal testing?
The biofilms are typically incubated with antifungals for 24 to 48 hours.
Is this method suitable for clinical applications?
Yes, it can be used to inform treatment decisions for fungal infections in clinical settings.

Nous décrivons une méthode simple, rapide et robuste pour la formation de

L’objectif global de cette procédure est de former des biofilms de candida albicans et d’examiner leur sensibilité aux agents antifongiques. Ceci est accompli en formant d’abord ces biofilms fongiques sur les puits de 96. Eh bien, des plaques de microtitration puis des antifongiques sont ajoutés aux biofilms préformés et incubés pendant 24 à 48 heures après cette incubation.

Une méthode cholémétrique qui mesure l’activité métabolique des cellules dans les biofilms est utilisée pour mesurer l’activité de ces antifongiques afin d’établir la concentration minimale inhibitrice d’antifongiques contre les biofilms. En fin de compte, des résultats peuvent être obtenus qui montrent la capacité de former des biofilms et des tests de sensibilité antifongique grâce à une méthode simple et facile basée sur une plaque de microtitration de 96 puits couplée à une lecture métrique de couleur. Le principal avantage de cette technique est qu’elle est facile, relativement peu coûteuse, hautement reproductible et qu’elle permet la formation de plusieurs biofilms équivalents.

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