O'Neill S L, Kittayapong P, Braig H R, Andreadis T G, Gonzalez J P, Tesh R B
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven , CT 06520-8034, USA.
J Gen Virol. 1995 Aug;76 ( Pt 8):2067-74. doi: 10.1099/0022-1317-76-8-2067.
A diagnostic PCR assay was designed based on conserved regions of previously sequenced densovirus genomic DNA isolated from mosquitoes. Application of this assay to different insect cell lines resulted in a number of cases of consistent positive amplification of the predicted size fragment. Positive PCR results were subsequently confirmed to correlate with densovirus infection by both electron microscopy and indirect fluorescent antibody test. In each case the nucleotide sequence of the amplified PCR fragments showed high identity to previously reported densoviruses isolated from mosquitoes. Phylogenetic analysis based on these sequences showed that two of these isolates were examples of new densoviruses. These viruses could infect and replicate in mosquitoes when administered orally or parenterally and these infections were largely avirulent. In one virus/mosquito combination vertical transmission to progeny was observed. The frequency with which these viruses were detected would suggest that they may be quite common in insect cell lines.
基于从蚊子中分离出的先前测序的浓核病毒基因组DNA的保守区域设计了一种诊断性PCR检测方法。将该检测方法应用于不同的昆虫细胞系,结果在许多情况下都一致扩增出了预测大小的片段。随后通过电子显微镜和间接荧光抗体试验证实,PCR阳性结果与浓核病毒感染相关。在每种情况下,扩增的PCR片段的核苷酸序列与先前报道的从蚊子中分离出的浓核病毒具有高度同源性。基于这些序列的系统发育分析表明,其中两个分离株是新浓核病毒的实例。这些病毒经口服或注射给药时可在蚊子体内感染和复制,且这些感染大多无致病性。在一种病毒/蚊子组合中,观察到了向子代的垂直传播。这些病毒的检测频率表明它们在昆虫细胞系中可能相当常见。