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Narasin, a novel antiviral compound that blocks dengue virus protein expression.
Antivir Ther. 2011; 16(8):1203-18.AT

Abstract

BACKGROUND

Dengue virus (DENV) is a mosquito-borne virus that causes a spectrum of human diseases ranging from mild dengue fever to dengue haemorrhagic fever and dengue shock syndrome in severe cases. Currently, there is no effective antiviral therapy or vaccine against DENV infection.

METHODS

In order to identify potential antiviral agents against DENV, we performed high-throughput cell-based screening on a highly purified natural products library. Among the screening hits, selected compounds which displayed 50-75% inhibition against DENV2 were validated using secondary assays. Time-of-addition studies, dose-dependent assays, real time quantitative reverse transcriptase (RT)-PCR, Western blot and ultrastructural imaging were conducted in an attempt to elucidate the potential antiviral mechanisms of narasin.

RESULTS

In this study, an ionophore, narasin was selected for detailed analysis due to its strong inhibitory profile against DENV infection with minimal cytotoxicity (50% cytotoxic concentration >1,000 μM). A dose-dependent study revealed narasin to have an 50% inhibitory concentration of less than 1 μM against all four serotypes of DENV. Time-of-addition studies of narasin-treated, DENV2-infected Huh-7 cells suggested narasin to be involved in inhibiting the post-entry stages of viral replication during DENV infection. Proteomic and ultrastructural analyses revealed the antiviral mechanism of narasin as likely to be associated with the disruption of viral protein synthesis. In addition, quantitative RT-PCR studies showed no differences in viral RNA levels between narasin-treated and control DENV2-infected cells.

CONCLUSIONS

Narasin was identified and characterized as a novel agent that inhibits DENV replication in vitro through non-cytotoxic mechanisms, thus indicating its potential to be further developed as a therapeutic anti-DENV agent.

Authors+Show Affiliations

Department of Microbiology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

22155902

Citation

Low, June Su Yin, et al. "Narasin, a Novel Antiviral Compound That Blocks Dengue Virus Protein Expression." Antiviral Therapy, vol. 16, no. 8, 2011, pp. 1203-18.
Low JS, Wu KX, Chen KC, et al. Narasin, a novel antiviral compound that blocks dengue virus protein expression. Antivir Ther. 2011;16(8):1203-18.
Low, J. S., Wu, K. X., Chen, K. C., Ng, M. M., & Chu, J. J. (2011). Narasin, a novel antiviral compound that blocks dengue virus protein expression. Antiviral Therapy, 16(8), 1203-18. https://doi.org/10.3851/IMP1884
Low JS, et al. Narasin, a Novel Antiviral Compound That Blocks Dengue Virus Protein Expression. Antivir Ther. 2011;16(8):1203-18. PubMed PMID: 22155902.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Narasin, a novel antiviral compound that blocks dengue virus protein expression. AU - Low,June Su Yin, AU - Wu,Kan Xing, AU - Chen,Karen Caiyun, AU - Ng,Mary Mah-Lee, AU - Chu,Justin Jang Hann, PY - 2011/12/14/entrez PY - 2011/12/14/pubmed PY - 2012/4/3/medline SP - 1203 EP - 18 JF - Antiviral therapy JO - Antivir Ther VL - 16 IS - 8 N2 - BACKGROUND: Dengue virus (DENV) is a mosquito-borne virus that causes a spectrum of human diseases ranging from mild dengue fever to dengue haemorrhagic fever and dengue shock syndrome in severe cases. Currently, there is no effective antiviral therapy or vaccine against DENV infection. METHODS: In order to identify potential antiviral agents against DENV, we performed high-throughput cell-based screening on a highly purified natural products library. Among the screening hits, selected compounds which displayed 50-75% inhibition against DENV2 were validated using secondary assays. Time-of-addition studies, dose-dependent assays, real time quantitative reverse transcriptase (RT)-PCR, Western blot and ultrastructural imaging were conducted in an attempt to elucidate the potential antiviral mechanisms of narasin. RESULTS: In this study, an ionophore, narasin was selected for detailed analysis due to its strong inhibitory profile against DENV infection with minimal cytotoxicity (50% cytotoxic concentration >1,000 μM). A dose-dependent study revealed narasin to have an 50% inhibitory concentration of less than 1 μM against all four serotypes of DENV. Time-of-addition studies of narasin-treated, DENV2-infected Huh-7 cells suggested narasin to be involved in inhibiting the post-entry stages of viral replication during DENV infection. Proteomic and ultrastructural analyses revealed the antiviral mechanism of narasin as likely to be associated with the disruption of viral protein synthesis. In addition, quantitative RT-PCR studies showed no differences in viral RNA levels between narasin-treated and control DENV2-infected cells. CONCLUSIONS: Narasin was identified and characterized as a novel agent that inhibits DENV replication in vitro through non-cytotoxic mechanisms, thus indicating its potential to be further developed as a therapeutic anti-DENV agent. SN - 2040-2058 UR - https://www.unboundmedicine.com/medline/citation/22155902/Narasin_a_novel_antiviral_compound_that_blocks_dengue_virus_protein_expression_ L2 - https://www.lens.org/lens/search/patent/list?q=citation_id:22155902 DB - PRIME DP - Unbound Medicine ER -