- Antiviral activity of Poncirus trifoliata seed extract against oseltamivirresistant influenza virus
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Yoonki Heo , Yeondong Cho , Kwon sung Ju , Hansam Cho , Ki Hoon Park , Hanul Choi , Jong Kwang Yoon , Chiung Moon , Young Bong Kim
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J. Microbiol. 2018;56(8):586-592. Published online July 25, 2018
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DOI: https://doi.org/10.1007/s12275-018-8222-0
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The emergence of oseltamivir-resistant variants of influenza
virus has highlighted the necessity for the development of
more effective novel antiviral drugs. To date, numerous researchers
have focused on developing antiviral drugs using
natural resources, such as traditional herbal medicines. Poncirus
trifoliata is widely used in oriental medicine as a remedy
for gastritis, dysentery, inflammation and digestive ulcers. In
this study, we investigated the potential antiviral effect of the
Poncirus trifoliata orange seed extract against influenza virus.
An ethanol extract of Poncirus trifoliata seeds (PTex) inhibited
the activity of influenza viruses, in particular, oseltamivir-
resistant strains, in Madin-Darby canine kidney cells. In
contrast to oseltamivir, PTex exerted a significant inhibitory
effect on the cellular penetration pathway of the virus rather
than HA receptor binding. The potent antiviral effect and novel
working mechanism of PTex support its further development
as an effective natural antiviral drug with a wide spectrum
of activity against influenza and oseltamivir-resistant
viruses.
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- Comparison of JEV Neutralization Assay Using Pseudotyped JEV with the Conventional Plaque-Reduction Neutralization Test
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Hee-Jung Lee , Kyung-Il Min , Ki Hoon Park , Hyo Jung Choi , Min-Kyoung Kim , Chi-Young Ahn , Young-Jin Hong , Young Bong Kim
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J. Microbiol. 2014;52(5):435-440. Published online March 7, 2014
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DOI: https://doi.org/10.1007/s12275-014-3529-y
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1,008
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We previously reported the development of a neutralization assay system for evaluating Japanese Encephalitis Virus (JEV) neutralizing antibody (NAb) using pseudotyped-JEV (JEV- PV). JEV-PV-based neutralization assay offers several advan-tages compared with the current standard plaque-reduc-tion neutralization test (PRNT), including simplicity, safety, and speed. To evaluate the suitability of the JEV-PV assay as new replacement neutralization assay, we compared its repeatability, reproducibility, specificity, and correlated its results with those obtained using the PRNT. These analyses showed a close correlation between the results obtained with the JEV-PV assay and the PRNT, using the 50% plaque re-duction method as a standard for measuring NAb titers to JEV. The validation results met all analytical acceptance criteria. These results suggest that the JEV-PV assay could serve as a safe and simple method for measuring NAb titer against JEV and could be used as an alternative approach for assaying the potency of JEV neutralization.
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