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      Siderophore Biosynthesis But Not Reductive Iron Assimilation Is Essential for Aspergillus fumigatus Virulence

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          Abstract

          The ability to acquire iron in vivo is essential for most microbial pathogens. Here we show that Aspergillus fumigatus does not have specific mechanisms for the utilization of host iron sources. However, it does have functional siderophore-assisted iron mobilization and reductive iron assimilation systems, both of which are induced upon iron deprivation. Abrogation of reductive iron assimilation, by inactivation of the high affinity iron permease (FtrA), has no effect on virulence in a murine model of invasive aspergillosis. In striking contrast, A. fumigatus l-ornithine- N 5-monooxygenase (SidA), which catalyses the first committed step of hydroxamate-type siderophore biosynthesis, is absolutely essential for virulence. Thus, A. fumigatus SidA is an essential virulence attribute. Combined with the absence of a sidA ortholog—and the fungal siderophore system in general—in mammals, these data demonstrate that the siderophore biosynthetic pathway represents a promising new target for the development of antifungal therapies.

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          Most cited references25

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          Aspergillus fumigatus and aspergillosis.

          J P Latgé (1999)
          Aspergillus fumigatus is one of the most ubiquitous of the airborne saprophytic fungi. Humans and animals constantly inhale numerous conidia of this fungus. The conidia are normally eliminated in the immunocompetent host by innate immune mechanisms, and aspergilloma and allergic bronchopulmonary aspergillosis, uncommon clinical syndromes, are the only infections observed in such hosts. Thus, A. fumigatus was considered for years to be a weak pathogen. With increases in the number of immunosuppressed patients, however, there has been a dramatic increase in severe and usually fatal invasive aspergillosis, now the most common mold infection worldwide. In this review, the focus is on the biology of A. fumigatus and the diseases it causes. Included are discussions of (i) genomic and molecular characterization of the organism, (ii) clinical and laboratory methods available for the diagnosis of aspergillosis in immunocompetent and immunocompromised hosts, (iii) identification of host and fungal factors that play a role in the establishment of the fungus in vivo, and (iv) problems associated with antifungal therapy.
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            The genetics of Aspergillus nidulans.

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              The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake.

              S. cerevisiae accumulate iron by a process requiring a ferrireductase and a ferrous transporter. We have isolated a mutant, fet3, defective for high affinity Fe(II) uptake. The wild-type FET3 gene was isolated by complementation of the mutant defect. Sequence analysis of the gene revealed the presence of an open reading frame coding for a protein with strong similarity to the family of blue multicopper oxidoreductases. Consistent with the role of copper in iron transport, growth of wild-type cells in copper-deficient media resulted in decreased ferrous iron transport. Addition of copper, but not other transition metals (manganese or zinc), to the assay media resulted in the recovery of Fe(II) transporter activity. We suggest that the catalytic activity of the Fet3 protein is required for cellular iron accumulation.
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                Author and article information

                Journal
                J Exp Med
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                1 November 2004
                : 200
                : 9
                : 1213-1219
                Affiliations
                [1 ]Department of Molecular Biology, Medical University Innsbruck, Peter-Mayr-Str. 4b/III, A-6020 Innsbruck, Austria
                [2 ]Department of Infectious Diseases, Imperial College London, London W12 0NN, England, UK
                Author notes

                Address correspondence to Hubertus Haas, Dept. of Molecular Biology, Medical University Innsbruck, Peter-Mayr-Str. 4b/III, A-6020 Innsbruck, Austria. Phone: 43-512-507-3605; Fax: 43-512-507-9880; email: hubertus.haas@ 123456uibk.ac.at

                Article
                20041242
                10.1084/jem.20041242
                2211866
                15504822
                dca1571b-62a6-45bc-987b-705613678858
                Copyright © 2004, The Rockefeller University Press
                History
                : 23 June 2004
                : 9 September 2004
                Categories
                Brief Definitive Report

                Medicine
                iron uptake,virulence factor,fungal pathogenicity,ornithine monooxygenase,aspergillosis
                Medicine
                iron uptake, virulence factor, fungal pathogenicity, ornithine monooxygenase, aspergillosis

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