The entire envelope gene of a British HIV-1 isolate, GB8, was cloned,
sequenced and aligned with those of the reference strains MN,SF2 and I
IIB/LAI. Three of the viruses (MN, IIIB/LAI, GB8) and their recombinan
t gp120s were then characterised using an extensive panel of human HIV
-1 positive sera and mapped neutralizing monoclonal antibodies (MAbs).
Overall, the GB8 env-gene translation product shares 84% homology wit
h those of the reference strains. Across the V3 region homology was gr
eater between GB8 and SF2/MN (74.3-66.7%) than IIIB/LAI (63.9-66.7%).
Accordingly, GB8 was sensitive to V3-specfic MAbs which neutralise MN/
SF2 and resistant to those which neutralise IIIB/LAI. In the CD4 bindi
ng region the central MWQEVGKAMYAPPI was conserved in all viruses but
homology in the N-terminus was greater between GB8 and SF2 and IIIB/LA
I than MN. GB8 and IIIB/LAI were sensitive to all MAbs raised against
the CD4 binding site whereas MN was resistant to 3 of 4 tested. Human
sera obtained from a London-based cohort did not differentiate between
GB8 and MN in neutralisation assays, whereas IIIB/LAI titres were sig
nificant lower at all stages of disease. These results show that GB8 c
arries a consensus-like V3 loop and is as reresentative as MN of HIV-1
viruses circulating in the UK. To our knowledge, GB8 is the only Brit
ish HIV-1 isolate which has been characterised to date.