HIV-1 group O has its epicenter in Cameroon and neighboring countries and i
s responsible for 3 to 5% of all HIV infections in this region. It is belie
ved that HIV-1 group O was introduced into the human population by a separa
te cross-species transmission, occurring independently of the HIV-1 (group
M and group N) and HIV-2 transmissions. We have studied the coreceptor requ
irements of 12 primary HIV-1 O-type isolates from individuals with differen
t clinical symptoms. Only 2 of these 12 viruses showed a syncytium-inducing
phenotype after infection of primary peripheral blood mononuclear cells (P
BMCs) and were infectious for the T cell line C8166, These isolates used CX
CR4 as a coreceptor for entry, whereas the remaining isolates used only CCR
5 efficiently. One isolate was able to use BOB and CCR8 as coreceptors in a
ddition to CXCR4 All group O isolates tested were efficiently inhibited by
SDF-1 or RANTES, the natural ligands of CXCR4 and CCR5, respectively. These
results indicate that CXCR4 and CCR5 are the principal coreceptors for HIV
-1 O-type viruses, Most of the HIV-1 group O isolates studied were derived
from patients at later stages of the disease. Although HIV-1 group O and gr
oup M infections do not differ in their pathogenesis, the studied isolates
did not evolve to use a broad range of coreceptors as described for HIV-1 g
roup hi and HIV-2.