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    Toll-like receptor 9-dependent immune activation by unmethylated CpG motifs in Aspergillus fumigatus DNA

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    Authors
    Ramirez-Ortiz, Zaida G.
    Specht, Charles A.
    Wang, Jennifer P.
    Lee, Chrono K.
    Bartholomeu, Daniella C.
    Gazzinelli, Ricardo T.
    Levitz, Stuart M.
    UMass Chan Affiliations
    Department of Medicine
    Document Type
    Journal Article
    Publication Date
    2008-03-12
    Keywords
    Animals
    Aspergillus fumigatus
    Cell Line
    Cells, Cultured
    CpG Islands
    Cytokines
    DNA, Fungal
    Dendritic Cells
    Endonucleases
    Humans
    Mice
    Mice, Inbred C57BL
    Oligodeoxyribonucleotides
    Site-Specific DNA Methyltransferase (Cytosine-Specific)
    Toll-Like Receptor 9
    Life Sciences
    Medicine and Health Sciences
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    Abstract
    Phagocytic defenses are critical for effective host defenses against the opportunistic fungal pathogen Aspergillus fumigatus. Previous studies found that following challenge with A. fumigatus, Toll-like receptor 9 (TLR9) knockout mice survived longer than wild-type mice. However, the mechanism responsible was not defined. Here we demonstrate that A. fumigatus contains unmethylated CpG sequences, the natural ligands for TLR9. A. fumigatus DNA and synthetic CpG-rich oligodeoxynucleotides (ODNs) containing sequences found in the A. fumigatus genome potently stimulated the production of proinflammatory cytokines in mouse bone marrow-derived dendritic cells (BMDCs) and human plasmacytoid dendritic cells. The response was decreased when the fungal DNA was treated with a CpG methylase or with CpG-specific endonucleases. A role for TLR9 was demonstrated as cytokine production was abolished in BMDCs from TLR9-deficient mice. Moreover, transfection of HEK293 cells with human TLR9 conferred responsiveness to synthetic CpG-rich ODNs containing sequences found in A. fumigatus DNA. Taken together, these data demonstrate that TLR9 detects A. fumigatus DNA, resulting in the secretion of proinflammatory cytokines, which may contribute to the immune response to the pathogen.
    Source
    Infect Immun. 2008 May;76(5):2123-9. Epub 2008 Mar 10. Link to article on publisher's site
    DOI
    10.1128/IAI.00047-08
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/39210
    PubMed ID
    18332208
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1128/IAI.00047-08
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    UMass Chan Faculty and Researcher Publications

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