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. 2010 Apr 28;48(7):2582–2585. doi: 10.1128/JCM.00082-10

TABLE 1.

Summary of techniques employed to quantify plasma SIV RNA

Assay Quantification systema Target region RNA extraction (plasma vol [μl]) Calibration/standards Upper and lower assay detection limits (RNA copies/ml) Real-time PCR platform Reference(s)
1 Real-time qRT-PCR p27-gag QIAamp, Qiagen (140) External SIV251 RNA plasma series 1 × 109 - 1.69 × 102 Mx3000P (Stratagene) 1
2 Conventional qRT-PCRc p27-gag Trizol, propan-2-ol (200) Coamplified synthetic RNA transcript 1 × 107 - 1.6 × 102 n/ab 27
3 Real-time qRT-PCR p27-gag QIAamp, Qiagen (200) SIV251 RNA transcript 1.6 × 106 - 1.69 × 102 ABI Prism (Applied Biosystems) 5, 18
4 qRT assay n/a Viral binding gel (1,000) BrdU/poly(A) system/HIV standard curve 1.2 ×106 - 2.3 × 102 n/a 3
5 Real-time qRT-PCRv p15-gag Nuclisens, bioMérieux (200) SIV251 and internal HIV-1 control 1 × 106 - 2.39 × 102 ABI Prism (Applied Biosystems) 20, 24, 25
6 Real-time qRT-PCR p27-gag Trizol (200) Coamplified synthetic RNA transcript 1 × 1010 - 2.3 × 102 iQ5 multicolor system (Bio-Rad) 10
a

qRT-PCR, quantitative reverse transcriptase PCR; qRT-PCRc, conventional qRT-PCR system based on endpoint estimation of preamplified product; qRT-PCRv, quantitative RT-PCR validated by a virion estimation technique. qRT assay (assay 4), ExaVir Load v. 2 (Cavidi AB, Uppsala, Sweden). Assay 6 is a previously established real-time PCR method (10), with a modification of the SIV probe sequence to the Black Hole Quencher 2 dye in place of TAMRA.

b

n/a, not applicable.