el Hussein A, Calisher C H, Holbrook F R, Schoepp R J, Beaty B J
Department of Microbiology, Colorado State University, Fort Collins.
J Clin Microbiol. 1989 Jun;27(6):1320-3. doi: 10.1128/jcm.27.6.1320-1323.1989.
A solid-phase enzyme immunoassay (EIA) was developed to detect bluetongue (BT) virus antigens in infected cell cultures and in suspensions of infected Culicoides variipennis midges. The technique was equally sensitive for detecting the five U.S. BT virus serotypes (2, 10, 11, 13, and 17) in cell cultures. EIA reliably detected about 3.8 log10 median tissue culture infective doses per ml of BT virus in infected cell culture lysates. The EIA readily detected virus antigens in pools of midges infected with BT serotypes 2, 10, 11, 13, and 17 and contained 2.3 to 4.8 log10 median tissue culture infective doses per ml of BT virus. The technique was sensitive enough to detect a single infected midge in a pool with 99 noninfected midges. The EIA may be a sensitive and rapid alternative to virus isolation for surveillance of BT viruses in vector populations.
开发了一种固相酶免疫测定法(EIA),用于检测感染细胞培养物和感染的库蠓(Culicoides variipennis)蠓悬液中的蓝舌病(BT)病毒抗原。该技术在检测细胞培养物中的五种美国BT病毒血清型(2、10、11、13和17)时同样灵敏。EIA能可靠地检测出感染细胞培养物裂解物中每毫升约3.8 log10半数组织培养感染剂量的BT病毒。EIA能轻松检测出感染了BT血清型2、10、11、13和17的蠓群中的病毒抗原,每毫升含2.3至4.8 log10半数组织培养感染剂量的BT病毒。该技术灵敏度足以在含有99只未感染蠓的蠓群中检测出一只感染的蠓。对于媒介种群中BT病毒的监测,EIA可能是一种替代病毒分离的灵敏且快速的方法。