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Broad-spectrum antivirals of protoporphyrins inhibit the entry of highly pathogenic emerging viruses

Authors :
Yuan Sun
Shengsheng Lu
Weijuan Shang
Sheng Fan
Xiaming Jiang
Yan Wu
Daiwei Chen
Xiaoyan Pan
Jian He
Xi Xie
Source :
Bioorganic Chemistry
Publication Year :
2020
Publisher :
Cold Spring Harbor Laboratory, 2020.

Abstract

Graphical abstract<br />Highlights • PPIX possesses broad antiviral activities in vitro against a panel of enveloped viruses. • PPIX interacts with the lipids of enveloped virions, thereby inhibiting the entry of enveloped viruses into host cells. • PPIX shows the antiviral effect in vivo by testing mice infected with the influenza A/Puerto Rico/8/34 (H1N1) virus.<br />Severe emerging and re-emerging viral infections such as Lassa fever, Avian influenza (AI), and COVID-19 caused by SARS-CoV-2 urgently call for new strategies for the development of broad-spectrum antivirals targeting conserved components in the virus life cycle. Viral lipids are essential components, and viral-cell membrane fusion is the required entry step for most unrelated enveloped viruses. In this paper, we identified a porphyrin derivative of protoporphyrin IX (PPIX) that showed broad antiviral activities in vitro against a panel of enveloped pathogenic viruses including Lassa virus (LASV), Machupo virus (MACV), and SARS-CoV-2 as well as various subtypes of influenza A viral strains with IC50 values ranging from 0.91 ± 0.25 μM to 1.88 ± 0.34 μM. A mechanistic study using influenza A/Puerto Rico/8/34 (H1N1) as a testing strain showed that PPIX inhibits the infection in the early stage of virus entry through biophysically interacting with the hydrophobic lipids of enveloped virions, thereby inhibiting the entry of enveloped viruses into host cells. In addition, the preliminary antiviral activities of PPIX were further assessed by testing mice infected with the influenza A/Puerto Rico/8/34 (H1N1) virus. The results showed that compared with the control group without drug treatment, the survival rate and mean survival time of the mice treated with PPIX were apparently prolonged. These data encourage us to conduct further investigations using PPIX as a lead compound for the rational design of lipid-targeting antivirals for the treatment of infection with enveloped viruses.

Details

Language :
English
Database :
OpenAIRE
Journal :
Bioorganic Chemistry
Accession number :
edsair.doi.dedup.....59079f125503f8d62f4351c015999eaf
Full Text :
https://doi.org/10.1101/2020.05.09.085811