Abstract

The Dengue (DENV) and zika (ZIKV) virus infections are currently a public health concern. At present, there is no treatment or a safe and effective vaccine for these viruses. Hence, the development of new strategies as host-directed therapy is required. In this sense, Metformin (MET), an FDA-approved drug used for the treatment of type 2 diabetes, has shown an anti-DENV effect in vitro by activating AMPK and reducing HMGCR activity. In this study, MET treatment was evaluated during in vitro and in vivo ZIKV infection and compared to MET treatment during DENV infection. Our results demonstrated that MET has a broad in vitro antiviral spectrum. MET inhibited ZIKV infection in different cell lines, but it was most effective in inhibiting DENV and yellow fever virus (YFV) infection in Huh-7 cells. However, the drug failed to protect against ZIKV infection when AG129 immunodeficient mice were used as in vivo model. Interestingly, MET increased DENV-infected male mice's survival time, reducing the severe signs of the disease. Together, these findings indicate that, although MET was an effective antiviral agent to inhibit in vitro and in vivo DENV infection, it could only inhibit in vitro ZIKV infection.

Highlights

  • The Dengue (DENV) and zika (ZIKV) virus infections are currently a public health concern

  • The selectivity index (SI) of MET based on the C­ C50/IC50 ratio was calculated in both cells

  • The MET cytotoxicity was similar in both cell lines; Huh-7 cells showed a ­CC50 of 32.9 mM and 33.43 mM in U-87 cells (Fig. 1A,B)

Read more

Summary

Introduction

The Dengue (DENV) and zika (ZIKV) virus infections are currently a public health concern. The development of new strategies as host-directed therapy is required In this sense, Metformin (MET), an FDA-approved drug used for the treatment of type 2 diabetes, has shown an anti-DENV effect in vitro by activating AMPK and reducing HMGCR activity. The genus flavivirus comprises more than 50 different viral species, and some of them are emerging in new geographic areas, such as dengue (DENV) and Zika virus (ZIKV). Both viruses can induce different clinical conditions ranging from fever to severe disease complications and even d­ eath[1,2]. Flavivirus infections are inhibited by drugs that reduce the synthesis and/or import of c­ holesterol[13,14]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call