Ting S H, See E, Tan H C, Lee M A, Ooi E E
Department of Microbiology, National University of Singapore, 5 Science Drive 2, Medical Faculty, 03-14, Singapore 117597, Singapore.
J Virol Methods. 2001 Apr;93(1-2):43-7. doi: 10.1016/s0166-0934(00)00293-7.
Japanese encephalitis virus is a common cause of viral encephalitis in Asia with an estimated 45,000 cases annually. It causes significant morbidity and mortality. It is transmitted primarily by Culex mosquitoes between birds and animals, while man is thought to be an accidental, dead-end host. Since dengue is also prevalent usually in Japanese encephalitis-endemic areas, all Japanese encephalitis positive sera must be confirmed by detecting Japanese encephalitis specific neutralizing antibodies. The plaque reduction neutralization test is the gold standard for detecting and quantifying Japanese encephalitis neutralizing antibodies. This test, however, takes about a week and is carried out in 6 or 24-well plates, which limits its usage for large-scale screening. A simplified assay was developed for the detection and quantification of Japanese encephalitis neutralizing antibodies. The assay, which is carried out in 96-well plates, would be suitable for use in the mass screening of the population's immunity level as well as for use in vaccine efficacy studies.
日本脑炎病毒是亚洲病毒性脑炎的常见病因,估计每年有45000例病例。它会导致严重的发病和死亡。它主要通过库蚊在鸟类和动物之间传播,而人类被认为是偶然的、终末宿主。由于登革热在日本脑炎流行地区通常也很普遍,所有日本脑炎阳性血清必须通过检测日本脑炎特异性中和抗体来确认。蚀斑减少中和试验是检测和定量日本脑炎中和抗体的金标准。然而,该试验需要大约一周时间,并且在6孔或24孔板中进行,这限制了其在大规模筛查中的应用。已开发出一种简化的检测方法用于检测和定量日本脑炎中和抗体。该检测方法在96孔板中进行,适用于人群免疫水平的大规模筛查以及疫苗效力研究。