Hildreth S W, Beaty B J
Am J Trop Med Hyg. 1984 Sep;33(5):965-72. doi: 10.4269/ajtmh.1984.33.965.
Enzyme immunoassays (EIAs) producing either chromogenic or fluorogenic end products were developed and evaluated for detection of eastern equine encephalomyelitis (EEE) and Highlands J (HJ) viruses in pools of Aedes triseriatus mosquitoes. Overnight incubation of the mosquito samples in the EIA significantly enhanced the sensitivity of the test. Both the EEE and HJ EIAs were sensitive, readily detecting one infected mosquito in a pool with 99 noninfected, and specific, distinguishing homologous from the alternate alphavirus and other arboviruses. By 3 days post-infection after intrathoracic inoculation, EEE virus was isolated from 100% (30/30) of the mosquitoes examined. Concurrently, EEE virus antigen was detectable by EIA in 100% (30/30) of examined mosquitoes and by indirect fluorescent antibody (IFA) technique in 77% (23/30) of the examined mosquito head squash preparations.
开发并评估了产生显色或荧光终产物的酶免疫测定法(EIA),用于检测三带喙库蚊群体中的东部马脑炎(EEE)病毒和高地J(HJ)病毒。将蚊虫样本在EIA中过夜孵育可显著提高检测的灵敏度。EEE和HJ的EIA均具有敏感性,能够轻易地在含有99只未感染蚊虫的样本中检测出1只感染蚊虫,且具有特异性,可区分同源的甲病毒与其他虫媒病毒及替代甲病毒。经胸腔接种后3天,从100%(30/30)的检测蚊虫中分离出EEE病毒。同时,通过EIA在100%(30/30)的检测蚊虫中可检测到EEE病毒抗原,而通过间接荧光抗体(IFA)技术在77%(23/30)的检测蚊虫头部压片标本中可检测到该抗原。