Jp. Riley et al., RELATIVE REACTIVITY OF THE V3 LOOP PND OF HIV-1 SUBTYPE-A, SUBTYPE-B,SUBTYPE-C, SUBTYPE-D, AND SUBTYPE-F WITH SERA FROM SELECTED UGANDAN LOCALITIES, Archives of virology, 140(8), 1995, pp. 1393-1404
Synthetic peptides comprising the predicted principal neutralizing det
erminant (PND) in new African and North American HIV-1 clones were tes
ted in ELISA for reactivity with ninety six serum samples from asympto
matic donors in six selected localities in Uganda. Irrespective of the
geographical origin of the samples, the majority of the test sera cro
ss-reacted at high intensities with the peptides derived from the nove
l North American clone, BRT3.6 (Group B), the Ugandan clone, CUG045, (
Group C), and the Romanian clone) FRMA (Group Fl. The frequency of rea
ctivity of the peptides from BRT3.6, CUG045, and FRMA were within the
ranges of 57-100%, 50-100%, and 57-100%, respectively, for the sera co
llected from these disparate localities. In contrast to these findings
, the V3 peptides derived from the other Ugandan isolates showed a mor
e restricted pattern of reactivity with the same serum samples: AUG06c
(1-63%), DUG23c (2%), and DUG044 (38-87%). The results from ELISA inh
ibition assay indicated that the V3 peptide from BRT 3.6, CUG045, and
FRMA express closely related antigenic specificities quite distinct fr
om those in AUG06c and DUG044. The residues comprising the PND in BRT3
.6, CUG045, and FRMA appear to be well conserved in the HIV-1 subtypes
prevalent in the selected Ugandan locales.