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Dengue virus is the causative agent of dengue fever (DF) and its complications;
dengue haemorrhagic fever (DHF) and dengue shock syndrome (DSS). It has
four serotypes (Dengue 1-4) and is a member of the family flaviridae. It is one of
the important causes of inorbidity and mortality through out the subtropical and
tropical regions, including Sri Lanka.
1. Patients with dengue need to be closely monitored for evidence of
haemorrhage and shock. In order to do this, it is necessary to differentiate patients
with dengue from non dengue patients. This however, is a challenge since dengue
often presents with non specific symptoms such as fever, headache and body
aches. Therefore, it requires an aetiological diagnosis based on laboratory
confirmation of disease. In this regard, an ideal diagnostic tool should be
sensitive, specific, reliable, rapid, cheap, technically less demanding and it should
also be able to detect dengue in the early stages of the disease. Detection of the circulating serotype IS very important In epidemiological surveillance of the
disease.
Laboratory diagnosis of dengue infection is normally based on detection of
dengue virus specific antibodies and isolation of dengue virus from patient's
serum. Serological diagnosis has been proven to be of less value in the early
stages of illness. Current technologies for isolation and identification of the
dengue virus are based on complicated systems such as suckling mouse brain or
mosquito inoculation or cell culture technique. These methods are technically
demanding, expensive and time consuming.
The availability of molecular diagnostics such as the Reverse Transcriptase
Polymerase Chain Reaction (RT-PCR) technique has made it possible to perform
rapid detection of the viral RNA. In this study, I present an alternative design of
the RT-PCR technique that can detect and simultaneously identify the sero type
ofthe dengue virus.
I designed sets of primers and developed an RT-PCR for rapid detection and
simultaneous identification of dengue virus and its serotypes in cell culture
supernatant and in serum samples. It was evaluated for sensitivity, specificity
and compared with other standard laboratory diagnostic methods. The test is
based on 5 sets of primer pairs specific -for dengue viruses within the nonstructural (NS) 5 region of the dengue virus genome. A universal primer set that
would bind to target sequence shared by all the four serotypes of the virus within
the NS5 region, are used. The resulting PCR products are detected by gel
electrophoresis and staining with ethidium bromide. The RT-PCR was
developed with serotype specific primers, which were also designed within the NS5 region of each serotype for the identification of dengue serotypes. The
amplified products of different sizes were obtained with different dengue
serotypes and were detected by gel electrophoresis. The RT-PCR technique is
simple and rapid, capable of not only detecting the dengue virus but also
identifying its serotype in clinical specimens. The RT-PCR protocol developed
by me was shown to more sensitive than virus isolation in cell culture and
equally sensitive in detecting dengue virus and its serotypes in serum specimens.
It was also shown not to cross react with other flaviviruses.
In the preliminary phylogenetic study, I compared the nucleotide sequence
homology of the Sri Lankan dengue virus isolates of the present study with
dengue viruses isolated form other parts of the world. Nucleotide sequence
analysis was performed by an automated nucleic acid sequencer on 14 dengue
virus isolates (13 dengue type 2 and one dengue type 3).
The dengue 2 viruses were most closely related to dengue 2 virus isolated in Sri
Lanka and Seychelle in 1990 and 1976 respectively. The dengue 3 virus was
most closely related to dengue 3 viruses recovered in Sri Lanka in 1991, 1985
and 1981. Our results suggested that these dengue virus serotypes are evolving
locally and any introduced strains are failing to become established.
