Detection and Differentiation of Genotype I and III Japanese Encephalitis Virus in Mosquitoes by Multiplex Reverse Transcriptase-Polymerase Chain Reaction

被引:9
|
作者
Chen, Y. Y. [1 ]
Lin, J. W. [1 ]
Fan, Y. C. [1 ]
Chiou, S. S. [1 ]
机构
[1] Natl Chung Hsing Univ, Grad Inst Microbiol & Publ Hlth, Coll Vet Med, Taichung 40227, Taiwan
关键词
Japanese encephalitis virus; mosquitoes; genotypes differentiation; multiplex RT-PCR; DENGUE VIRUS; PCR; PROTEINS; SAMPLES; TAIWAN; ASSAY; ASIA;
D O I
10.1111/j.1865-1682.2012.01369.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Japanese encephalitis (JE) is a disease that threatens both human and animal populations in Asian countries, and the causative agent of JE, Japanese encephalitis virus (JEV), has recently changed from genotype III (GIII) to genotype I (GI). However, a test for the rapid differentiation of GI and GIII JEV is still unavailable, especially one that can be used for mosquito-based surveillance. We have designed GI- and GIII-specific primer sets for the rapid detection and differentiation of GI and GIII JEV by multiplex reverse transcriptase-polymerase chain reaction (multiplex RT-PCR). The GI-specific and GIII-specific primer sets were able to specifically amplify the target gene from GI and GIII JEV, respectively. The limitations of detection were 0.00225 and 0.225 pfu for the GI-specific and GIII-specific primers, respectively. Using a mixture of GI-specific and GIII-specific primers, the multiplex RT-PCR was able to specifically detect and differentiate GI and GIII JEV. The multiplex RT-PCR was able to successfully differentiate GI and GIII virus in JEV-infected mosquitoes. Thus, a sensitive and specific multiplex RT-PCR system for the rapid detection and differentiation of GI and GIII JEV has been developed, and this test is likely to be valuable when carrying out mosquito-based JEV surveillance.
引用
收藏
页码:37 / 43
页数:7
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