Development and field evaluation of a nested RT-PCR kit for detecting Japanese encephalitis virus in mosquitoes

被引:18
作者
Jeong, Young Eui [1 ]
Jeon, Min Ju [1 ]
Cho, Jung Eun [1 ]
Han, Myung Guk [1 ]
Choi, Hwan Ju [2 ]
Shin, Mi Yeong [3 ]
Park, Hag Jae [3 ]
Kim, Woosik [4 ]
Moon, Bong Chun [5 ]
Park, Ji-Sung [6 ]
Park, Bona [6 ]
Ju, Young Ran [1 ]
机构
[1] Korea Ctr Dis Control & Prevent, WHO Japanese Encephalitis Reg Reference Lab Weste, Div Arboviruses, Natl Inst Hlth, Seoul 122701, South Korea
[2] Gyeong Nam Res Inst Hlth & Environm, Changwon Si 641702, Gyeongsangnam, South Korea
[3] Jeon Nam Res Inst Hlth & Environm, Kwangju 502200, South Korea
[4] Chung Nam Res Inst Hlth & Environm, Taejon 300801, South Korea
[5] Inst Environm Resource Res Jeju Special Self Gove, Jeju City 690817, Jeju Do, South Korea
[6] JungAng Induspia BD, Dept Mfg & Dev, Intron Biotechnol Inc, Gyeonggi Do 462120, South Korea
关键词
Japanese encephalitis virus; Nested RT-PCR; Mosquito; Surveillance; South Korea; WEST-NILE-VIRUS; RNA;
D O I
10.1016/j.jviromet.2010.11.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel nested reverse transcription-polymerase chain reaction (RT-PCR)-based kit is described for detecting Japanese encephalitis virus (JEV), especially for genotype 1 and 3 strains. The assay consists of a first round RT-PCR and a subsequent nested PCR amplification. It has unique features such as the use of a premix system in which all reagents are lyophilized in reaction tubes and the inclusion of control RNA in each reaction to monitor false negative results. In addition, an automatic tissue homogenizer and a RNA extraction system are used concurrently for assay standardization and increasing throughput. The assay using the kit proved specific for JEV with no amplification of other JEV-related flaviviruses. The detection limits were approximately 0.1 PFU/ml and 1 PFU/ml for JEV genotypes 1 and 3, respectively. The assay protocol has been validated in large-scale field trials in South Korea during the 2008-2009 surveillance seasons. Nineteen of 1136 pools of mosquitoes (54,583 mosquitoes total) were identified as JEV positive. This nested RT-PCR kit combined with control RNA and an automatic RNA extraction system should be suitable for routine JEV surveillance programs. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:248 / 252
页数:5
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