| Literature DB >> 28457610 |
Malika Aid1, Peter Abbink1, Rafael A Larocca1, Michael Boyd1, Ramya Nityanandam1, Ovini Nanayakkara1, Amanda J Martinot1, Edward T Moseley1, Eryn Blass1, Erica N Borducchi1, Abishek Chandrashekar1, Amanda L Brinkman1, Katherine Molloy1, David Jetton1, Lawrence J Tartaglia1, Jinyan Liu1, Katharine Best2, Alan S Perelson2, Rafael A De La Barrera3, Mark G Lewis4, Dan H Barouch5.
Abstract
Zika virus (ZIKV) is associated with severe neuropathology in neonates as well as Guillain-Barré syndrome and other neurologic disorders in adults. Prolonged viral shedding has been reported in semen, suggesting the presence of anatomic viral reservoirs. Here we show that ZIKV can persist in cerebrospinal fluid (CSF) and lymph nodes (LN) of infected rhesus monkeys for weeks after virus has been cleared from peripheral blood, urine, and mucosal secretions. ZIKV-specific neutralizing antibodies correlated with rapid clearance of virus in peripheral blood but remained undetectable in CSF for the duration of the study. Viral persistence in both CSF and LN correlated with upregulation of mechanistic target of rapamycin (mTOR), proinflammatory, and anti-apoptotic signaling pathways, as well as downregulation of extracellular matrix signaling pathways. These data raise the possibility that persistent or occult neurologic and lymphoid disease may occur following clearance of peripheral virus in ZIKV-infected individuals.Entities:
Keywords: CSF; Zika; infection; lymph node; mTOR; persistence; rhesus; sanctuaries; transcriptomics; viral dynamics
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Year: 2017 PMID: 28457610 PMCID: PMC5426912 DOI: 10.1016/j.cell.2017.04.008
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582