Journal Browser Advanced Search Help
Journal Browser Advanced search HELP
-
J Bacteriol Virol. 2016 Dec;46(4):231-238. English. Original Article. https://doi.org/10.4167/jbv.2016.46.4.231
Yang DK , Kim HH , Jo HY , Choi SS , Cho IS .
Viral Disease Division, Animal and Plant Quarantine Agency, Gyeongsangbuk-do, Korea. yangdk@korea.kr
Abstract

Japanese encephalitis (JE) is a zoonosis that affects the nervous system of humans and other animals. The genotype of JE virus (JEV) has shifted recently from genotype 3 (G3) to genotype 1 (G1) in Asia, including Korea. Thus, a rapid differential assay is required to make an accurate diagnosis of JEV genotype. In this study, we designed common and differential primer sets for JEV G1 and G3 to detect the JEV envelope (E) gene. The specific primer sets for JEV G1 and G3 specifically amplified the target gene. The detection limits of the three primer sets were 10(1.0), 10(2.0), and 10(2.0) TCID₅₀/reaction, respectively. No cross-reactivity was detected with non-JEV reference viruses. The multiplex reverse transcription-polymerase chain reaction (RT-PCR) assay specifically differentiated JEV G1 from G3. Thus, a one-step multiplex RT-PCR assay was established to rapidly and differentially detect JEV. This assay will be useful for confirming JEV infections in animals and checking the JEV genotype in veterinary biological products.

Copyright © 2019. Korean Association of Medical Journal Editors.