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Investigation of BKPyV life cycle, activation of innate immune responses and membrane remodeling in microvascular endothelial cells

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Author
Bruštíková, KateřinaWoS Profile - HLX-3084-2023Scopus Profile - 57200960906
Rjabčenko, BorisORCiD Profile - 0000-0001-7076-256XWoS Profile - U-8964-2017Scopus Profile - 36142246600
Liebl, DavidORCiD Profile - 0000-0002-1899-7713WoS Profile - AFJ-1224-2022Scopus Profile - 6701661958
Horníková, LenkaORCiD Profile - 0000-0003-1539-8413WoS Profile - L-7348-2017Scopus Profile - 13105604900
Forstová, JitkaORCiD Profile - 0000-0003-0219-506XWoS Profile - L-7328-2017Scopus Profile - 6701385419
Huerfano Meneses, SandraORCiD Profile - 0000-0001-5221-3014WoS Profile - G-8469-2013Scopus Profile - 6506988916

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Publication date
2024
Published in
Czech Chemical Society Symposium Series
Publisher / Publication place
Česká společnost chemická
Volume / Issue
22 (6)
ISBN / ISSN
ISSN: 2336-7202
ISBN / ISSN
eISSN: 2336-7210
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  • Faculty of Science
Abstract
Polyomaviruses (PyVs) are small double-stranded DNA viruses that occur widely in nature. Among the 14 known human PyVs, three are particularly relevant: BK Polyomavirus (BKPyV), JC polyomavirus, and Merkel cell carcinoma Polyomavirus. BKPyV, with a global prevalence of approximately 80% in adults, typically causes asymptomatic primary infection. After initial infection, it disseminates via the bloodstream and establishes persistence in the urinary tract. Reactivation of BKPyV can occur in immunocompromised patients, leading to complications such as nephritis or graft loss1-2. Unfortunately, there are currently no specific antiviral treatments available for BKPyV infection.
Keywords
polyomaviruses (PyVs), HMVECs bd, STING, BKPyV
Permanent link
https://hdl.handle.net/20.500.14178/2657
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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