| Literature DB >> 30053656 |
Ronik Khachatoorian1, Whitaker Cohn2, Anthony Buzzanco3, Rana Riahi4, Vaithilingaraja Arumugaswami5, Asim Dasgupta6, Julian P Whitelegge7, Samuel W French8.
Abstract
Zika virus (ZIKV) has been identified as a cause of neurologic diseases in infants and Guillain-Barré Syndrome, and currently, no therapeutics or vaccines are approved. In this study, we sought to identify potential host proteins interacting with ZIKV particles to gain better insights into viral infectivity. Viral particles were purified through density-gradient centrifugation and subsequently, size-exclusion chromatography (SEC). Mass spectrometric analyses revealed viral envelope protein and HSP70 to comigrate in only one SEC fraction. Neither of these proteins were found in any other SEC fractions. We then performed neutralization assays and found that incubating viral particles with antibody against HSP70 indeed significantly reduced viral infectivity, while HSC70 antibody did not. Preincubating cells with recombinant HSP70 also decreased viral infectivity. Knockdown and inhibition of HSP70 also significantly diminished viral production. These results implicate HSP70 in the pathogenesis of ZIKV and identify HSP70 as a potential host therapeutic target against ZIKV infection.Entities:
Keywords: Heat shock proteins HSP70 HSC70 Zika virus
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Year: 2018 PMID: 30053656 DOI: 10.1016/j.virol.2018.07.009
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616