Zhang Y M, Hayes E P, McCarty T C, Dubois D R, Summers P L, Eckels K H, Chanock R M, Lai C J
Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Virol. 1988 Aug;62(8):3027-31. doi: 10.1128/JVI.62.8.3027-3031.1988.
We have constructed a recombinant baculovirus containing a 4.0-kilobase dengue virus cDNA sequence that codes for the three virus structural proteins, capsid (C) protein, premembrane (PreM) protein, and envelope glycoprotein (E), and nonstructural proteins NS1 and NS2a. Infection of cultured Spodoptera frugiperda cells with this recombinant virus resulted in the production of E and NS1 proteins that were similar in size to the corresponding viral proteins expressed in dengue virus-infected simian cells. Other dengue virus-encoded proteins such as PreM and C were also synthesized. Rabbits immunized with the dengue virus protein products of the recombinant virus developed antibodies to PreM, E, and NS1, although the titers were low, especially to PreM and E. Nevertheless, the dengue virus antigens produced by the recombinant virus induced resistance in mice to fatal dengue encephalitis.
我们构建了一种重组杆状病毒,其包含一个4.0千碱基的登革病毒cDNA序列,该序列编码三种病毒结构蛋白,即衣壳(C)蛋白、前膜(PreM)蛋白和包膜糖蛋白(E),以及非结构蛋白NS1和NS2a。用这种重组病毒感染培养的草地贪夜蛾细胞,导致产生的E蛋白和NS1蛋白大小与在登革病毒感染的猴细胞中表达的相应病毒蛋白相似。还合成了其他登革病毒编码的蛋白,如PreM和C。用重组病毒的登革病毒蛋白产物免疫的兔子产生了针对PreM、E和NS1的抗体,尽管效价较低,尤其是针对PreM和E的效价。然而,重组病毒产生的登革病毒抗原在小鼠中诱导了对致命性登革脑炎的抗性。