| Literature DB >> 29288700 |
Zhong Li1, Srilatha Sakamuru2, Ruili Huang2, Matthew Brecher1, Cheri A Koetzner1, Jing Zhang1, Haiying Chen3, Cheng-Feng Qin4, Qing-Yu Zhang5, Jia Zhou3, Laura D Kramer5, Menghang Xia2, Hongmin Li6.
Abstract
Many flaviviruses, such as Zika virus (ZIKV), Dengue virus (DENV1-4) and yellow fever virus (YFV), are significant human pathogens. Infection with ZIKV, an emerging mosquito-borne flavivirus, is associated with increased risk of microcephaly in newborns and Guillain-Barré syndrome and other complications in adults. Currently, specific therapy does not exist for any flavivirus infections. In this study, we found that erythrosin B, an FDA-approved food additive, is a potent inhibitor for flaviviruses, including ZIKV and DENV2. Erythrosin B was found to inhibit the DENV2 and ZIKV NS2B-NS3 proteases with IC50 in low micromolar range, via a non-competitive mechanism. Erythrosin B can significantly reduce titers of representative flaviviruses, DENV2, ZIKV, YFV, JEV, and WNV, with micromolar potency and with excellent cytotoxicity profile. Erythrosin B can also inhibit ZIKV replication in ZIKV-relevant human placental and neural progenitor cells. As a pregnancy category B food additive, erythrosin B may represent a promising and easily developed therapy for management of infections by ZIKV and other flaviviruses.Entities:
Keywords: Antiviral; Dengue virus; Erythrosin B; Flavivirus; Protease inhibitor; Zika virus
Mesh:
Substances:
Year: 2017 PMID: 29288700 PMCID: PMC5892443 DOI: 10.1016/j.antiviral.2017.12.018
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970