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
Author
Shubitz, Lisa FPowell, 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 ArizonaDepartment 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
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Oxford University PressCitation
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.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 2020ISSN
1537-6613PubMed ID
32658292Version
Final accepted manuscriptae974a485f413a2113503eed53cd6c53
10.1093/infdis/jiaa419
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