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. 2014 May 23;9(5):e98077. doi: 10.1371/journal.pone.0098077

Table 2. Detection of integrated HIV-1 genome in epithelial cells by qPCR.

Cell line R5-YU2 (MOI  = 7.5) X4-LAI (MOI  = 10) X4-LAI (MOI  = 140)
FaDu ND Not included ND
TR146 ND ND ND
A431 ND ND ND
C8166a n/a + (Ct  =  33) + (Ct  = 33)
NP2-R5b + (Ct  = 29) n/a n/a
a

C8166 cells express CXCR4 and were used for X4 viral infections only.

b

NP2-R5 cells express CCR5 and were used for R5 viral infections only.

+, Integrated HIV-1 product detected (cycle threshold detection in brackets).

ND, Integrated HIV-1 product not detected.

Real-time PCR assay to detect integrated HIV-DNA using HIV-1 LTR and human Alu-specific primers and a U5 specific probe [92]. TR146, FaDu, A431 and PM-1 (control) cells were exposed to YU2 (R5) or LAI (X4) virus for 48 h at 37°C. DNA was extracted, digested with DpnI to degrade any plasmid DNA contaminant and analysed by real-time PCR.