Abstract:
Arboviruses (arthropod-borne viruses) are viruses that are maintained in nature through
transmission between susceptible vertebrate hosts by haematophagous arthropods. These viruses
multiply and produce viraemia in the vertebrates, replicate In the tissue of arthropods, and are then
passed on to new vertebrates by the bites of these arthropods (Simpson, 1984).
There are 504 arboviruses registered in the International Catalogue of Arboviruses (Labuda, 1991)
of which approximately 100 are capable of infecting man. The majority of arboviruses have been
serologically classified in the families; Togaviridae, Flaviviridae, Reoviridae, Bunyaviridae, and
Rhabdoviridae.
Mosquitoes are the most important arbovirus vectors, followed by ticks. Phlebotomines,
Culicoides species and Cimex species are also involved in the transmission of some arboviruses
(Simpson, 1984).
Studies have shown that Sindbis (SIN), West Nile (WN), Rift Valley fever (RVF) and Wesselsbron
(WSL) viruses are the most prevalent arboviruses in the Orange Free State (Mcintosh, 1980) and
with generalised clinical symptoms such as fever, headache, general malaise, muscle or jOint pains
and a macular or maculopapular rash (Lennette & Schmidt, 1979) a conclusive diagnosis for
arbovirus infections can only be made by the laboratory.
Standard tests for identifying viruses or detecting viral antibodies are often time consuming,
expensive and necessitate sophistication. No commercial diagnostic kits are available for detecting
antibodies to certain arbovlruses, therefore, it was necessary to develop a simple, cost-effective
test for screening and determining specific antibodies of the immunoglobulin G (lgG) and
Immunoglobulin M (lgM) class against RVF, SIN, WN and WSL viruses.
In the conventional enzyme-linked immunosorbent assays (ELISA) for detecting viral antigens and
antibodies, polystyrene or other materials (which have a rather low binding capacity for proteins)
are generally used as the solid phase. On the other hand, the superior binding capacity of
nitrocellulose (NC) for the adsorption of proteins from a polyacrylamide gel following
electrophoresis by the Western blot technique, has been demonstrated and implicated the
advantageous use of NC instead of polystyrene as the solid phase (Towbin et al. 1979). The aim of this study was to develop a dot-ELISA by using a NC membrane as solid phase on
which to spot antigens for later visualisation of antigen-antibody complexes of RVF, SIN, WN and
WSL with enzyme-conjugated anti-human immunoglobulins of the IgG, as well as the IgM class,
using a substrate which gives an insoluble colour reaction.
