Sensing of oxygen in microtiter plates: a novel tool for screening drugs against pathogenic yeasts

Anal Bioanal Chem. 2008 Jul;391(5):1731-7. doi: 10.1007/s00216-008-1947-6. Epub 2008 Feb 24.

Abstract

Most antibiotics were discovered via their inhibition of growth of target organisms. However, yeasts in particular have the capability to adapt metabolic pathways to the availability of nutrients e.g. yeasts can easily switch between respiratory and fermentative pathways in response to oxygen concentration, or can even use both simultaneously. Thus, we cultivated S. cerevisiae BY4741 and C. albicans 1386 in microtiter plates with integrated oxygen sensors to characterize the availability of oxygen for the organisms and to detect influences of fungicides on the oxygen consumption rates. The relevance of the respiratory pathway was indicated by the almost total consumption of oxygen during the first 1-3 h of the cultivation in the microtiter plates, when an increase in turbidity could hardly be seen. Moreover, the sensitivity of S. cerevisiae to inhibitors of the respiratory chain, such as myxothiazol, could be detected via a reduced oxygen consumption rate, whereas no inhibition of growth was observed. Thus, not only was the sensitivity of the test organism for the test compound detectable, but the affected pathway was also highlighted. Other compounds, such as pyrrolnitrin and ambruticin VS-3, inhibited growth of C. albicans 1386 and of S. cerevisiae (only pyrrolnitrin), which was additionally observed as reduced oxygen consumption rates. Thus, the determination of oxygen in microtiter plates via fluorescent dyes is a versatile supplement to standard growth inhibition tests.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / pharmacology*
  • Biosensing Techniques / methods*
  • Candida albicans / growth & development
  • Drug Evaluation, Preclinical
  • Fluorescent Dyes / chemistry*
  • Methacrylates
  • Oxygen / analysis*
  • Oxygen / metabolism
  • Oxygen Consumption / drug effects*
  • Oxygen Consumption / physiology
  • Pyrrolnitrin
  • Saccharomyces cerevisiae
  • Sensitivity and Specificity
  • Spectrometry, Fluorescence / instrumentation
  • Spectrometry, Fluorescence / methods*
  • Thiazoles
  • Yeasts / drug effects*
  • Yeasts / growth & development
  • Yeasts / metabolism

Substances

  • Antifungal Agents
  • Fluorescent Dyes
  • Methacrylates
  • Thiazoles
  • myxothiazol
  • Pyrrolnitrin
  • Oxygen