Abstract
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.
Full Text
The Full Text of this article is available as a PDF (634.4 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Abel P. P., Nelson R. S., De B., Hoffmann N., Rogers S. G., Fraley R. T., Beachy R. N. Delay of disease development in transgenic plants that express the tobacco mosaic virus coat protein gene. Science. 1986 May 9;232(4751):738–743. doi: 10.1126/science.3457472. [DOI] [PubMed] [Google Scholar]
- Chambers T. J., Hahn C. S., Galler R., Rice C. M. Flavivirus genome organization, expression, and replication. Annu Rev Microbiol. 1990;44:649–688. doi: 10.1146/annurev.mi.44.100190.003245. [DOI] [PubMed] [Google Scholar]
- Chanas A. C., Gould E. A., Clegg J. C., Varma M. G. Monoclonal antibodies to Sindbis virus glycoprotein E1 can neutralize, enhance infectivity, and independently inhibit haemagglutination or haemolysis. J Gen Virol. 1982 Jan;58(Pt 1):37–46. doi: 10.1099/0022-1317-58-1-37. [DOI] [PubMed] [Google Scholar]
- Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
- Crampton J., Morris A., Lycett G., Warren A., Eggleston P. Transgenic mosquitoes: a future vector control strategy? Parasitol Today. 1990 Feb;6(2):31–36. doi: 10.1016/0169-4758(90)90057-b. [DOI] [PubMed] [Google Scholar]
- Denhardt D. T. Mechanism of action of antisense RNA. Sometime inhibition of transcription, processing, transport, or translation. Ann N Y Acad Sci. 1992 Oct 28;660:70–76. doi: 10.1111/j.1749-6632.1992.tb21059.x. [DOI] [PubMed] [Google Scholar]
- Deubel V., Kinney R. M., Trent D. W. Nucleotide sequence and deduced amino acid sequence of the structural proteins of dengue type 2 virus, Jamaica genotype. Virology. 1986 Dec;155(2):365–377. doi: 10.1016/0042-6822(86)90200-x. [DOI] [PubMed] [Google Scholar]
- Gould E. A., Buckley A., Cammack N., Barrett A. D., Clegg J. C., Ishak R., Varma M. G. Examination of the immunological relationships between flaviviruses using yellow fever virus monoclonal antibodies. J Gen Virol. 1985 Jul;66(Pt 7):1369–1382. doi: 10.1099/0022-1317-66-7-1369. [DOI] [PubMed] [Google Scholar]
- Gubler D. J., Clark G. G. Dengue/dengue hemorrhagic fever: the emergence of a global health problem. Emerg Infect Dis. 1995 Apr-Jun;1(2):55–57. doi: 10.3201/eid0102.952004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hahn C. S., Hahn Y. S., Braciale T. J., Rice C. M. Infectious Sindbis virus transient expression vectors for studying antigen processing and presentation. Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2679–2683. doi: 10.1073/pnas.89.7.2679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hahn Y. S., Galler R., Hunkapiller T., Dalrymple J. M., Strauss J. H., Strauss E. G. Nucleotide sequence of dengue 2 RNA and comparison of the encoded proteins with those of other flaviviruses. Virology. 1988 Jan;162(1):167–180. doi: 10.1016/0042-6822(88)90406-0. [DOI] [PubMed] [Google Scholar]
- Halstead S. B. Pathogenesis of dengue: challenges to molecular biology. Science. 1988 Jan 29;239(4839):476–481. doi: 10.1126/science.3277268. [DOI] [PubMed] [Google Scholar]
- Henchal E. A., Gentry M. K., McCown J. M., Brandt W. E. Dengue virus-specific and flavivirus group determinants identified with monoclonal antibodies by indirect immunofluorescence. Am J Trop Med Hyg. 1982 Jul;31(4):830–836. doi: 10.4269/ajtmh.1982.31.830. [DOI] [PubMed] [Google Scholar]
- Higgs S., Olson K. E., Klimowski L., Powers A. M., Carlson J. O., Possee R. D., Beaty B. J. Mosquito sensitivity to a scorpion neurotoxin expressed using an infectious Sindbis virus vector. Insect Mol Biol. 1995 May;4(2):97–103. doi: 10.1111/j.1365-2583.1995.tb00013.x. [DOI] [PubMed] [Google Scholar]
- Higgs S., Powers A. M., Olson K. E. Alphavirus expression systems: applications to mosquito vector studies. Parasitol Today. 1993 Dec;9(12):444–452. doi: 10.1016/0169-4758(93)90098-z. [DOI] [PubMed] [Google Scholar]
- Kawano H., Rostapshov V., Rosen L., Lai C. J. Genetic determinants of dengue type 4 virus neurovirulence for mice. J Virol. 1993 Nov;67(11):6567–6575. doi: 10.1128/jvi.67.11.6567-6575.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lindbo J. A., Dougherty W. G. Untranslatable transcripts of the tobacco etch virus coat protein gene sequence can interfere with tobacco etch virus replication in transgenic plants and protoplasts. Virology. 1992 Aug;189(2):725–733. doi: 10.1016/0042-6822(92)90595-g. [DOI] [PubMed] [Google Scholar]
- Marchuk D., Drumm M., Saulino A., Collins F. S. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. Nucleic Acids Res. 1991 Mar 11;19(5):1154–1154. doi: 10.1093/nar/19.5.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Monath T. P. Dengue: the risk to developed and developing countries. Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2395–2400. doi: 10.1073/pnas.91.7.2395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murray J. M., Aaskov J. G., Wright P. J. Processing of the dengue virus type 2 proteins prM and C-prM. J Gen Virol. 1993 Feb;74(Pt 2):175–182. doi: 10.1099/0022-1317-74-2-175. [DOI] [PubMed] [Google Scholar]
- Olson K. E., Higgs S., Hahn C. S., Rice C. M., Carlson J. O., Beaty B. J. The expression of chloramphenicol acetyltransferase in Aedes albopictus (C6/36) cells and Aedes triseriatus mosquitoes using a double subgenomic recombinant Sindbis virus. Insect Biochem Mol Biol. 1994 Jan;24(1):39–48. doi: 10.1016/0965-1748(94)90121-x. [DOI] [PubMed] [Google Scholar]
- Osatomi K., Sumiyoshi H. Complete nucleotide sequence of dengue type 3 virus genome RNA. Virology. 1990 Jun;176(2):643–647. doi: 10.1016/0042-6822(90)90037-r. [DOI] [PubMed] [Google Scholar]
- Powers A. M., Olson K. E., Higgs S., Carlson J. O., Beaty B. J. Intracellular immunization of mosquito cells to LaCrosse virus using a recombinant Sindbis virus vector. Virus Res. 1994 Apr;32(1):57–67. doi: 10.1016/0168-1702(94)90061-2. [DOI] [PubMed] [Google Scholar]
- Ramanathan M., MacGregor R. D., Hunt C. A. Predictions of effect for intracellular antisense oligodeoxyribonucleotides from a kinetic model. Antisense Res Dev. 1993 Spring;3(1):3–18. doi: 10.1089/ard.1993.3.3. [DOI] [PubMed] [Google Scholar]
- Raviprakash K., Liu K., Matteucci M., Wagner R., Riffenburgh R., Carl M. Inhibition of dengue virus by novel, modified antisense oligonucleotides. J Virol. 1995 Jan;69(1):69–74. doi: 10.1128/jvi.69.1.69-74.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rice C. M., Levis R., Strauss J. H., Huang H. V. Production of infectious RNA transcripts from Sindbis virus cDNA clones: mapping of lethal mutations, rescue of a temperature-sensitive marker, and in vitro mutagenesis to generate defined mutants. J Virol. 1987 Dec;61(12):3809–3819. doi: 10.1128/jvi.61.12.3809-3819.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Haan P., Gielen J. J., Prins M., Wijkamp I. G., van Schepen A., Peters D., van Grinsven M. Q., Goldbach R. Characterization of RNA-mediated resistance to tomato spotted wilt virus in transgenic tobacco plants. Biotechnology (N Y) 1992 Oct;10(10):1133–1137. doi: 10.1038/nbt1092-1133. [DOI] [PubMed] [Google Scholar]