Unexpected Link between Metal Ion Deficiency and Autophagy in <i>Aspergillus fumigatus</i>

  • Daryl L. Richie
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529
  • Kevin K. Fuller
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529
  • Jarrod Fortwendel
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529
  • Michael D. Miley
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529
  • Jason W. McCarthy
    Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461
  • Marta Feldmesser
    Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York 10461
  • Judith C. Rhodes
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529
  • David S. Askew
    Department of Pathology & Laboratory Medicine, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267-0529

Bibliographic Information

Published
2007-12
Rights Information
  • https://journals.asm.org/non-commercial-tdm-license
DOI
  • 10.1128/ec.00224-07
Publisher
American Society for Microbiology

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Description

<jats:title>ABSTRACT</jats:title> <jats:p> Autophagy is the major cellular pathway for bulk degradation of cytosolic material and is required to maintain viability under starvation conditions. To determine the contribution of autophagy to starvation stress responses in the filamentous fungus <jats:italic>Aspergillus fumigatus</jats:italic> , we disrupted the <jats:italic>A. fumigatus atg1</jats:italic> gene, encoding a serine/threonine kinase required for autophagy. The ΔAf <jats:italic>atg1</jats:italic> mutant showed abnormal conidiophore development and reduced conidiation, but the defect could be bypassed by increasing the nitrogen content of the medium. When transferred to starvation medium, wild-type hyphae were able to undergo a limited amount of growth, resulting in radial expansion of the colony. In contrast, the ΔAf <jats:italic>atg1</jats:italic> mutant was unable to grow under these conditions. However, supplementation of the medium with metal ions rescued the ability of the ΔAf <jats:italic>atg1</jats:italic> mutant to grow in the absence of a carbon or nitrogen source. Depleting the medium of cations by using EDTA was sufficient to induce autophagy in wild-type <jats:italic>A. fumigatus</jats:italic> , even in the presence of abundant carbon and nitrogen, and the ΔAf <jats:italic>atg1</jats:italic> mutant was severely growth impaired under these conditions. These findings establish a role for autophagy in the recycling of internal nitrogen sources to support conidiophore development and suggest that autophagy also contributes to the recycling of essential metal ions to sustain hyphal growth when exogenous nutrients are scarce. </jats:p>

Journal

  • Eukaryotic Cell

    Eukaryotic Cell 6 (12), 2437-2447, 2007-12

    American Society for Microbiology

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