To investigate the presence of Lagos bat virus (LBV)-specifi c antibodies in megachiroptera from West Africa, we conducted fl uorescent antibody virus neutralization tests. Neutralizing antibodies were detected in Eidolon helvum (37%), Epomophorus gambianus (3%), and Epomops buettikoferi (33%, 2/6) from Ghana. These fi ndings confi rm the presence of LBV in West Africa.
Bats host a range of lyssaviruses, depending on their species and locality. The genus Lyssavirus is differentiated into 7 genetically divergent genotypes: classical rabies virus (genotype 1), Lagos bat virus (LBV; genotype 2), Mokola virus (MOKV; genotype 3), Duvenhage virus (genotype 4), European bat lyssavirus (genotypes 5 and 6), and Australian bat lyssavirus (genotype 7) (1). All but MOKV have been isolated from bats.LBV and MOKV are each distributed in Africa and are members of phylogroup 2 within the genus Lyssavirus (1). Because LBV isolates (2) from African bats are increasing, our goal was to determine the prevalence of virus neutralizing antibodies against LBV in bat populations in West Africa.
The StudyBats were sampled in January and May 2007 at 6 sites in Ghana: the center of Accra (urban habitat); the wooded outskirts of Accra (savannah habitat); and forested habitats at Pra, Kibi, Adoagyiri, and Oyibi (a plantation with woodland/forest border). Bats were captured by using 6-18-m mist nets; roosting Eidolon helvum were captured by using nets on poles. A sample size of 59 would provide 95% confi dence of fi nding at least 1 LBV-seropositive bat in a large population (>5,000), given a seroprevalence of 5% and assuming random sampling (3). Species were identifi ed by using a dichotomous key (4). Captured bats were manually restrained and anesthetized by intravenous injection; ≈0.2-1.0 mL of blood was collected from the propatagial vein before the bat was released. Blood was centrifuged in the fi eld at ambient temperature at 3,000 rpm for 15 min. Serum was heat treated at 56°C for 30 min and frozen at -70°C.Two species, Epomophorus gambianus and E. helvum, were caught in suffi cient numbers (117 and 66, respectively) for reasonable inferences to be made about LBV seroprevalence rates (Table). A standard approach was used to calculate 95% confi dence intervals (CIs) for seroprevalence (3). Because of the relatively short distances between study sites and the likelihood of bats mixing between these sites, bats of each species were considered to belong to single populations. All but 3 E. helvum were derived from a colony in Accra, whereas E. gambianus were derived from all habitat types.Bat serum samples were tested for virus neutralizing antibody against classical rabies virus (challenge virus standard) by using a standard fl uorescent antibody virus neutralization (FAVN) test (5). Antibodies to LBV were measured by using a modifi ed FAVN test (6). Because positive bat antiserum from naturally infected bats was not available, for positive controls we used human rabies immunoglobulin, LBV-positive rabbit serum, and serum from mice vaccina...