| dc.contributor.author |
Hapugoda, M.D. |
en_US |
| dc.contributor.author |
Gunasekera, M.B. |
en_US |
| dc.contributor.author |
de Silva, N.R. |
en_US |
| dc.contributor.author |
Gunasena, S. |
en_US |
| dc.contributor.author |
Prithimala, L.D. |
en_US |
| dc.contributor.author |
Dayanath, M.Y.D. |
en_US |
| dc.contributor.author |
Abeyewickreme, W. |
en_US |
| dc.date.accessioned |
2015-08-29T23:40:11Z |
en_US |
| dc.date.available |
2015-08-29T23:40:11Z |
en_US |
| dc.date.issued |
2003 |
en_US |
| dc.identifier.citation |
The Bulletin of the Sri Lanka College of Microbiologists. 2003:1(1):30-31 |
en_US |
| dc.identifier.uri |
http://repository.kln.ac.lk/handle/123456789/9362 |
en_US |
| dc.description |
Oral Presentation Abstract (OP19), Proceedings of the Annual Academic Sessions of
Sri Lanka College of Microbiologists 19-21 June 2003, MRI, Colombo Sri Lanka |
en_US |
| dc.description.abstract |
Dengue is an important public health problem. In this study an RT-PCR-LH assay was developed for the detection of dengue virus in Ae.albopictus, a vector of dengue. Laboratory bred Ae.albopictus (adults inoculated with dengue prototypes were tested by RT-PCR-LH assay. RT-PCR products of NS3 gene of 4 dengue prototypes were hybridized in liquid phase with 32P) labelled cocktail of dengue serotype-specific ologonucliotides. Semi-Nested-PCR agarose gel electrophoresis (Semi-Nested-PCR-AGE) assay with dengue type specific oligonucliotides was carried out for typing of RT-PCR products. Wild-caught Ae.albopictus (larvae (n=89 pools) and adults (n=69 pools) collected from dengue case reported stations during the period of 1999-2002 were also tested by RT-PCR-LH and typed by Nested-PCR-AGE assay). A DNA band (470bp) specific for dengue virus was observed in all pools of Ae.albopictus (inoculated with dengue prototypes in RT-PCR-LH assay. When RT-PCR products of dengue prototypes inoculated mosquitoes were typed by Semi-Nested-PCR-AGE assay, bands of 169,362, 265, 426 bp sizes corresponding to DEN1, DEN2, DEN3 and DEN4 respectively were observed. The DNA band specific for dengue virus (470bp) was also observed in 6 pools of wild-caught adults in RT-PCR-LH assay. They were found to be infected with DEN3 (265bp DEN3 specific DNA band was detected) by Semi-Nested-PCR-AGE assay. None of the wild-caught larvae showed dengue specific DNA band (470bp) in RT-PCR-LH assay). RT-PCR-LH with Semi-Nested-PCR-AGE assays are useful for the detection and typing of dengue virus in Ae.albopictus. Ae.albopictus (in Sri Lanka is competent in transmitting DEN3 and possibly other serotypes. Detection of dengue virus for the first time in Ae.albopictus in Sri Lanka confirms earlier observations that it may play an important role in transmitting dengue). Acknowledgements: Financial assistance by the International Atomic Energy Agency (Technical Co¬operation grant no SLR/ 06 / 024) and University of Kelaniya (Research grant no RP/03/04/06/01/00) is gratefully acknowledged. |
en_US |
| dc.language.iso |
en_US |
en_US |
| dc.publisher |
Sri Lanka College of Microbiologists |
en_US |
| dc.subject |
Dengue |
en_US |
| dc.subject |
Dengue Virus |
en_US |
| dc.subject |
Dengue-diagnosis |
en_US |
| dc.subject |
Reverse Transcriptase Polymerase Chain Reaction |
en_US |
| dc.subject |
Reverse Transcriptase Polymerase Chain Reaction-methods |
en_US |
| dc.title |
Detection of dengue virus in Aedes albopictus mosquitoes by Reverse Transcription Polymerase-Chain Reaction-Liquid Hybridization (RT-PCR-LH) based assay. |
en_US |
| dc.type |
Conference Abstract |
en_US |
| dc.identifier.department |
Molecular Medicine Unit |
en_US |
| dc.identifier.department |
Parasitology |
en_US |