The bacterial secondary metabolite 2,4-diacetylphloroglucinol impairs mitochondrial function and affects calcium homeostasis in Neurospora crassa

Danielle M. Troppens, Meiling Chu, Lucy J. Holcombe, Olive Gleeson, Fergal O'Gara, Nick D. Read, John P. Morrissey

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The bacterial secondary metabolite 2,4-diacetylphloroglucinol (DAPG) is of interest as an active ingredient of biological control strains of Pseudomonas fluorescens and as a potential lead pharmaceutical molecule because of its capacity to inhibit growth of diverse microbial and non-microbial cells. The mechanism by which this occurs is unknown and in this study the filamentous fungus Neurospora crassa was used as a model to investigate the effects of DAPG on a eukaryotic cell. Colony growth, conidial germination and cell fusion assays confirmed the inhibitory nature of DAPG towards N. crassa. A number of different fluorescent dyes and fluorescent protein reporters were used to assess the effects of DAPG treatment on mitochondrial and other cellular functions. DAPG treatment led to changes in mitochondrial morphology, and rapid loss of mitochondrial membrane potential. These effects are likely to be responsible for the toxicity of DAPG. It was also found that DAPG treatment caused extracellular calcium to be taken up by conidial germlings leading to a transient increase in cytosolic free Ca2+ with a distinct concentration dependent Ca2+ signature. © 2013 Elsevier Inc.
    Original languageEnglish
    Pages (from-to)135-146
    Number of pages11
    JournalFungal Genetics and Biology
    Volume56
    DOIs
    Publication statusPublished - Jul 2013

    Keywords

    • Antimicrobial
    • Calcium
    • DAPG
    • Mitochondria
    • Neurospora crassa

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