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Published on: June 26, 2020
Virocidal activity of Egyptian scorpion venoms against hepatitis C virus
Alaa M H El-Bitar1,2, Moustafa M H Sarhan3, Chie Aoki4
1Department of Zoology, Faculty of Science, Al-Azhar University, Assiut, Egypt. sci.elbitar@gmail.com.
Background:
Hepatitis C virus (HCV) is a major global health problem, causing chronic hepatitis, liver cirrhosis and hepatocellular carcinoma. Development of well-tolerated regimens with high cure rates and fewer side effects is still much needed. Recently, natural antimicrobial peptides (AMPs) are attracting more attention as biological compounds and can be a good template to develop therapeutic agents, including antiviral agents against a variety of viruses. Various AMPs have been characterized from the venom of different venomous animals including scorpions.
Methods:
The possible antiviral activities of crude venoms obtained from five Egyptian scorpion species (Leiurus quinquestriatus, Androctonus amoreuxi, A. australis, A. bicolor and Scorpio maurus palmatus) were evaluated by a cell culture method using Huh7.5 cells and the J6/JFH1-P47 strain of HCV. Time-of-addition experiments and inactivation of enzymatic activities of the venoms were carried out to determine the characteristics of the anti-HCV activities.
Results:
S. maurus palmatus and A. australis venoms showed anti-HCV activities, with 50% inhibitory concentrations (IC₅₀) being 6.3 ± 1.6 and 88.3 ± 5.8 μg/ml, respectively. S. maurus palmatus venom (30 μg/ml) impaired HCV infectivity in culture medium, but not inside the cells, through virocidal effect. The anti-HCV activity of this venom was not inhibited by a metalloprotease inhibitor or heating at 60°C. The antiviral activity was directed preferentially against HCV.
Conclusions:
S. maurus palmatus venom is considered as a good natural source for characterization and development of novel anti-HCV agents targeting the entry step. To our knowledge, this is the first report describing antiviral activities of Egyptian scorpion venoms against HCV, and may open a new approach towards discovering antiviral compounds derived from scorpion venoms.
Insights
Egyptian scorpion venoms show potential as a new source for Hepatitis C virus (HCV) treatments. Scorpio maurus palmatus venom effectively inhibited HCV infectivity, offering a novel antiviral strategy.
Area of Science:
- Biochemistry
- Virology
- Pharmacology
Background:
- Hepatitis C virus (HCV) infection is a significant global health concern, leading to severe liver diseases.
- Existing treatments for HCV require improvement in terms of tolerability and efficacy.
- Natural antimicrobial peptides (AMPs), particularly from scorpion venom, are emerging as promising templates for antiviral drug development.
Purpose of the Study:
- To investigate the antiviral activities of crude venoms from five Egyptian scorpion species against Hepatitis C virus (HCV).
- To characterize the mechanism of action and specificity of any observed anti-HCV effects.
Main Methods:
- Crude venoms from five Egyptian scorpion species were tested for anti-HCV activity using Huh7.5 cells and the J6/JFH1-P47 HCV strain.
- Time-of-addition experiments and enzymatic activity inactivation were performed to elucidate the anti-HCV mechanism.
Main Results:
- Scorpio maurus palmatus and Androctonus australis venoms exhibited significant anti-HCV activity, with IC50 values of 6.3 ± 1.6 μg/ml and 88.3 ± 5.8 μg/ml, respectively.
- S. maurus palmatus venom demonstrated a virocidal effect, impairing HCV infectivity in the culture medium but not intracellularly.
- The anti-HCV activity of S. maurus palmatus venom was heat-stable and unaffected by metalloprotease inhibitors, indicating a specific antiviral action.
Conclusions:
- Scorpio maurus palmatus venom is a promising natural source for developing novel anti-HCV agents that target the viral entry stage.
- This study represents the first report of antiviral activity of Egyptian scorpion venoms against HCV.
- Scorpion venom-derived compounds may offer a new therapeutic avenue for Hepatitis C treatment.
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