Gaines P J, Olson K E, Higgs S, Powers A M, Beaty B J, Blair C D
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Colorado State University, Fort Collins, Colorado 80523, USA.
J Virol. 1996 Apr;70(4):2132-7. doi: 10.1128/JVI.70.4.2132-2137.1996.
The full-length premembrane (prM) coding region of the dengue virus type 2 (DEN-2; Jamaica) genome was expressed in C6/36 (Aedes albopictus) cells in either the sense or the antisense orientation from a double subgenomic Sindbis (dsSIN) virus. Northern (RNA) blot analysis confirmed the expression of sense or antisense DEN-2 prM RNA in infected C6/36 cells. PrM protein was demonstrated in cells infected with dsSIN virus expressing DEN-2 sense RNAs by an immunofluorescence assay. C6/36 cells were infected with each dsSIN virus at a multiplicity of infection (MOI) of 50 and challenged 48 h later with DEN-2 virus at an MOI of 0.1. Whereas C6/36 cells infected with a control of dsSIN virus supported high levels of DEN-2 replication, C6/36 cells infected with the dsSIN virus expressing prM antisense RNA were completely resistant to DEN-2 challenge. Cells expressing prM protein or untranslatable prM sense RNA also were resistant to DEN-2 challenge. Cells expressing prM protein demonstrated some breakthrough of DEN-2 virus when challenged at an MOI of 10. However, expressed untranslatable sense prM RNA conferred complete protection to challenge at the high MOI.
登革2型病毒(DEN-2;牙买加株)基因组的全长膜前体(prM)编码区,以正义或反义方向,从双亚基因组辛德毕斯病毒(dsSIN)在白纹伊蚊C6/36细胞中表达。Northern(RNA)印迹分析证实了在受感染的C6/36细胞中正义或反义DEN-2 prM RNA的表达。通过免疫荧光测定法在感染了表达DEN-2正义RNA的dsSIN病毒的细胞中证实了PrM蛋白的存在。以50的感染复数(MOI)用每种dsSIN病毒感染C6/36细胞,并在48小时后以0.1的MOI用DEN-2病毒攻击。虽然用dsSIN病毒对照感染的C6/36细胞支持高水平的DEN-2复制,但用表达prM反义RNA的dsSIN病毒感染的C6/36细胞对DEN-2攻击完全有抗性。表达prM蛋白或不可翻译的prM正义RNA的细胞对DEN-2攻击也有抗性。当以1•0的MOI进行攻击时,表达prM蛋白的细胞表现出一些DEN-2病毒突破。然而,表达的不可翻译的正义prM RNA在高MOI攻击时提供了完全保护。