Antiviral activity of ouabain against a Brazilian Zika virus strain

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作者
Deyse Cristina Madruga Carvalho
Poliana Gomes da Silva
Willyenne Marília Dantas
Severino Jefferson Ribeiro da Silva
Caroline Targino Alves da Silva
Elton José Ferreira Chaves
Demetrius Antônio Machado de Araújo
Ronaldo Nascimento de Oliveira
Sandra Rodrigues-Mascarenhas
Lindomar José Pena
机构
[1] Federal University of Paraiba (UFPB),Laboratory of Immunobiotechnology, Biotechnology Center
[2] Aggeu Magalhães Institute (IAM),Department of Virology and Experimental Therapy
[3] Oswaldo Cruz Foundation (Fiocruz),Laboratory of Molecular and Cellular Biotechnology, Department of Biotechnology
[4] Federal University of Paraiba (UFPB),Department of Chemistry
[5] Federal Rural University of Pernambuco (UFRPE),undefined
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Scientific Reports | / 12卷
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摘要
Zika virus (ZIKV) is an emerging arbovirus associated with neurological disorders. Currently, no specific vaccines or antivirals are available to treat the ZIKV infection. Ouabain, a cardiotonic steroid known as Na+/K+-ATPase inhibitor, has been previously described as an immunomodulatory substance by our group. Here, we evaluated for the first time the antiviral activity of this promising substance against a Brazilian ZIKV strain. Vero cells were treated with different concentrations of ouabain before and after the infection with ZIKV. The antiviral effect was evaluated by the TCID50 method and RT-qPCR. Ouabain presented a dose-dependent inhibitory effect against ZIKV, mainly when added post infection. The reduction of infectious virus was accompanied by a decrease in ZIKV RNA levels, suggesting that the mechanism of ZIKV inhibition by ouabain occurred at the replication step. In addition, our in silico data demonstrated a conformational stability and favorable binding free energy of ouabain in the biding sites of the NS5-RdRp and NS3-helicase proteins, which could be related to its mechanism of action. Taken together, these data demonstrate the antiviral activity of ouabain against a Brazilian ZIKV strain and evidence the potential of cardiotonic steroids as promising antiviral agents.
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