Rapid identification of virus-carrying mosquitoes using reverse transcription-loop-mediated isothermal amplification

被引:8
|
作者
Perera, Namal [1 ,2 ]
Aonuma, Hiroka [1 ,3 ]
Yoshimura, Aya [1 ]
Teramoto, Tokiyasu [1 ]
Iseki, Hiroshi [1 ]
Nelson, Bryce [1 ]
Igarashi, Ikuo [1 ]
Yagi, Takeshi [3 ]
Fukumoto, Shinya [1 ]
Kanuka, Hirotaka [1 ]
机构
[1] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, Obihiro, Hokkaido 0808555, Japan
[2] Med Res Inst, Colombo 08, Sri Lanka
[3] Osaka Univ, Grad Sch Frontier Biosci, Labs Integrated Biol, KOKORO Biol Grp, Suita, Osaka 5650871, Japan
关键词
LAMP; Diagnosis; Virus; Mosquito; FHV; FLOCK HOUSE VIRUS;
D O I
10.1016/j.jviromet.2008.10.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mosquitoes are critical vectors in many arboviral transmission cycles. Considering the increasing incidence of arboviral infections throughout the world, monitoring of vector populations for the presence of an arbovirus could be considered an important initial step of risk assessment to humans and animals. In response to this need, increased efforts to develop rapid and reliable diagnostic techniques have been undertaken; a single-step reverse transcription-loop-mediated isothermal amplification (RT-LAMP) assay was developed to detect virus in vector mosquitoes (Aedes aegypti) using the Flock House Virus (FHV) as a model. The robustness of the RT-LAMP reaction was revealed by its ability to detect FHV from an "all-in-one" template using whole mosquito bodies within 30 min. Furthermore, RT-LAMP identified successfully a mosquito carrying just a single FHV particle, a level easily overlooked in conventional analysis such as plaque forming assays. These observations suggest that RT-LAMP is more reliable and useful for routine diagnosis of vector mosquitoes in regions where the prevalence of vector-borne diseases such as West Nile fever or dengue fever are common. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 36
页数:5
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