Polymerase chain reaction (PCR) combined with non-radioactive DNA hybr
idization was applied for the detection and characterization of a 150
bp tandem repeat of Onchocerca volvulus. DNA of worms from western Uga
nda was amplified and then probed with a digoxygenin-labelled oligonuc
leotide, specific for the forest form of O. volvulus and compared to s
amples from various African countries. Hybridization was only observed
with PCR products from the forest in Liberia, south-eastern Ghana, Be
nin and southern Cameroon, but not with worms from Uganda or the savan
nah in Burkina Faso and northern Ghana. A nested PCR using primers der
ived form the forest form-specific DNA sequence confirmed these result
s. Morphometric studies revealed length differences between the microf
ilariae of Ugandan O. volvulus to those of West Africa, especially to
those of the savannah in Burkina Faso. It is concluded that the forest
/savannah classification of O. volvulus from West Africa is not suitab
le for Simulium neavei-transmitted O. volvulus from Uganda.