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. 2005 Oct;79(19):12575–12583. doi: 10.1128/JVI.79.19.12575-12583.2005

TABLE 1.

Infectivity, in vitro replicative capacity, and IC50 values of sera and sCD4 against mutant strains lacking glycosylation sites proximal to CD4 contact residuesa

Viral strain Infectivity (% of WT) Growth in tissue culture IC50 sera (inverse dilution) IC50 sCD4 (ng/μl)
SIV239 NA Yes <20 17.8
g3 170 Yes <20 4.0
g11 8 Yes <20 3.6
g16 35 Yes 15 39.0
g19 65 Yes 20 6.0
g20 33 Yes <20 24.0
g22 69 Yes <20 16.0
g23 82 Yes <20 12.0
g3,11 14 Yes <20 3.5
g19,20 12 Yes <20 22.0
g22,23 59 Yes <20 9.0
g14,22,23 2 Yesb NA NA
g16,22,23 0 No NA NA
g19,20,22,23 33 Yes 30 32
g3,11,19,20 17 Yes >20 9.4
g16,19,20,22,23 0 No NA NA
g14,19,20,22,23 0 No NA NA
g15,19,20,22,23 0 No NA NA
g11,19,20,22,23 2 No NA NA
a

NA, nonapplicable due to low to no infectivity.

b

Replication was noted by day 32, and sequencing of reverse transcription-PCR products derived from cell-free virus revealed nonsynonymous substitutions that were likely compensatory. The mutants in boldface type are those with enhanced neutralization sensitivity to sCD4.