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. 2013 Nov;57(11):5649–5657. doi: 10.1128/AAC.01536-13

Table 1.

Summary of emergent substitutions in selection experiments using CBMCsa

Virusb Subtype Background substitution(s) Drug(s) Selected substitution(s)
8336 B A98S, G190A EFV K101E
NL4-3 WT B None EFV K101E, V108I
10583 C Y181C EFV K101E/K, V106M, Y181C
8116 B A98S, G190A DPV K101E, Y181C
NL4- -Y181C B Y181C DPV K101E, V179I, Y181C
NL4-3-Y181C B Y181C DPV-TDF K101K/E, V108I/V, V179I/V, Y181C, H221Y
10583 C Y181C DPV-TDF K101E/K, V108I/V, V179I/V, Y181C, H221Y
Mole 03c C None ETR-FTC K101E/K, E138E/K
Mole 03d C None ETR-FTC E138K, M184I.
Mole 03 C None ETR-3TC K101E, M184I
a

Selection experiments were performed over 19 weeks. Abbreviations: 3TC, lamivudine; DPV, dapivirine; EFV, efavirenz; ETR, etravirine; FTC, emtricitabine; TDF, tenofovir disoproxil fumarate.

b

Viruses other than NL4-3 clones are clinical isolates from treatment-naive patients undergoing acute HIV-1 infection.

c

Viruses were genotyped at week 13.

d

Viruses were genotyped at week 19.