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. 2012 Jun 21;8(6):e1002774. doi: 10.1371/journal.ppat.1002774

Table 1. Ultrasensitive viral load measurements.

Macaque Time (in days) Viral RNA (copies/mL) Spike copies original count (RNA copies/mL)
P157 204 and 239 (see Fig. 2) <3 * 7008
P185 204 and 239 (see Fig. 2) <3 * 10822
P188 204 and 239 (see Fig. 2) <3 * 8194
P177 312 and 347 (see Fig. 8) <3 * 7692
§591 and 599 (see Fig. 8) <3 ** 6062
§654 and 658 (see Fig. 8) <3 ** 9060
P252 §215 and 365 (see Fig. 8) <3 ** 6201
4416 238 and 272 (see Fig. 4) <3 * 8276
BD12 98 and 105 (see Fig. 4) <3 ** 9319
BD53 98 and 105 (see Fig. 4) <3 ** 8494
BD64 400 and 407 (see Fig. 4) <3 * 18997
BD69 381 and 388 (see Fig. 4) 27 * 8900
429 and 437 (see Fig. 4) <4 (less plasma) ** 5569
451 and 458 (see Fig. 4) <3 *** 20

Shown are the real time PCR viral RNA measurements of pooled plasma samples (two pooled samples per measurement; total plasma volume 6 mL; detection limit = 3 RNA copies/mL). The time points selected for the analyses are shown as days from the zero point adopted in figures 2, 4 and 8. In these time points, the macaques were under H-iART (unmarked), or off-treatment after therapy suspension (marked with “§”). As a control of the assay variability and to exclude PCR inhibition, spiked RNA measurements for each plasma sample are shown. The RNA copy numbers (in copies/mL) used for the spiked measurements were: * 8686; ** 8605; *** 34. The low copy number spike was chosen to double-check the absence of low-level viremia in macaque BD69 that was the only one showing detectable viral RNA during the first PCR run.