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. 2016 Sep 6;13(1):64. doi: 10.1186/s12977-016-0298-1

Table 1.

Clinical history of variants encoding L domain-2 mutations

Participanta Viral RNA loadb CD4 + countc ARTd L-Domain 2e CVL PL
PRI NRTI NNRTI Resistance mutationsa
CVL PLf PR RT
4 4.74 5.87 113 RTV, IDV d4T, ABC NVP No Yes FYPLDSL 1/12
LYPLDSL 8/8 8/12
29 5.32 6.17 107 ddI, 3TC No No LCPLDSL 1/20
LYPLDSL 8/8 8/8
30 4.4 5.2 76 ABC, AZT, 3TC NVP No Yes LYPTDSL 16/16
LYPLTASL 8/10
31 3.56 4.71 161 4dT, 3TC No Yes QYPLASL 1/9
LYPLDSL 8/10 12/12
36 5.7 4.08 167 SQV 4dT, 3TC No No MYPLTAL 11/11 16/16
37 5.68 5.3 171 4dT No No LYPLTFL 2/21
39 3.72 4.57 158 SQV No  No MYPLTSL 16/16

aAs designated in Kemal et al. [26]

bLog copies/ml in plasma at time of sampling

cCells/ml at time of sampling

dART reported by participant at time of sampling: abacavir (ABC); zidovudine (AZT)’ stavudine (d4T); indinavir (IDV); nevirapine (NVP); ritonavir (RTV); didanosine (ddI); lamivudine (3TC); saquinavir (SQV)

eBold font, mutation relative to NL4-3 concensus sequence in Gag p6: LYPL(A or T)SL

fOrigin of variants, Cervical lavage (CVL); plasma (PL); numbers indicate the frequency among single genome variants