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    A Chronic Murine Disease Model of Coccidioidomycosis Using Coccidioides posadasii, Strain 1038

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    Shubitz accepted Cp1038.pdf
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    Final Accepted Manuscript
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    Author
    Shubitz, Lisa F
    Powell, Daniel A
    Butkiewicz, Christine D
    Lewis, M Lourdes
    Trinh, Hien T
    Frelinger, Jeffrey A
    Orbach, Marc J
    Galgiani, John N
    Affiliation
    Valley Fever Center for Excellence, University of Arizona
    Department of Immunobiology, University of Arizona
    United States, School of Plant Sciences, University of Arizona
    Department of Medicine, University of Arizona
    Issue Date
    2020-07-13
    Keywords
    Coccidioides
    B6D2
    chronic
    cytokines
    interferon γ
    mice
    Survival
    TNF-α
    
    Metadata
    Show full item record
    Publisher
    Oxford University Press
    Citation
    Shubitz, L. F., Powell, D. A., Butkiewicz, C. D., Lewis, M. L., Trinh, H. T., Frelinger, J. A., ... & Galgiani, J. N. (2021). A chronic murine disease model of coccidioidomycosis using Coccidioides posadasii, strain 1038. The Journal of Infectious Diseases, 223(1), 166-173.
    Journal
    The Journal of Infectious Diseases
    Rights
    © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Murine infections with most Coccidioides spp. strains are lethal by 3 weeks, limiting the study of immune responses. Coccidioides posadasii, strain 1038 (Cp1038), while slowly lethal, resulted in protracted survival of C57BL/6 (B6) mice. In resistant (B6D2)F1/J mice, lung fungal burdens stabilized by week 4 without progression through week 16, better modeling human coccidioidal infections after their immunologic control. Immunodeficient tumor necrosis factor (Tnf) α knockout (KO) and interferon (Ifn) γ receptor 1 (Ifn-γr1) KO mice survived a median of 22.5 and 34 days, compared with 70 days in B6 mice (P = .001 and P < .01, respectively), though 14-day lung fungal burden studies showed little difference between Ifn-γr1 KO and B6 mice. B6 mice showed peak concentrations of key inflammatory lung cytokines, including interleukin 6, 23, and 17A, Tnf-α, and Ifn-γ, only after 4 weeks of infection. The slower progression in B6 and the acquired fungal burden stability in B6D2 mice after Cp1038 infection greatly increases the array of possible immunologic studies. © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
    Note
    12 month embargo; published online 13 July 2020
    ISSN
    1537-6613
    PubMed ID
    32658292
    DOI
    10.1093/infdis/jiaa419
    Version
    Final accepted manuscript
    ae974a485f413a2113503eed53cd6c53
    10.1093/infdis/jiaa419
    Scopus Count
    Collections
    UA Faculty Publications

    entitlement

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