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. 2011 Jun;49(6):2169–2174. doi: 10.1128/JCM.00101-11

Table 1.

Serum PCR positivity when testing simulated serum specimens spiked with various genomic burdens

Fungal burden (no. of ge/0.5 ml serum) MycAssay Aspergillus PCRa
In-house Aspergillus PCRa
Cq difference (no. of cycles)
% positivity Mean no. of Cq cycles (SD) % positivity Mean no. of Cq cycles (SD)
50,000 (nd = 2) 100 24.1 (0.1) 100 24.4 (0.2) 0.3
5,000 (n = 3) 100 27.8 (0.5) 100 28.8 (1.3) 1.0
500 (n = 4) 100 31.4 (0.3) 100 33.1 (0.6) 1.7
100 (n = 3) 100 33.8 (1.6) 100 35.4 (1.5) 1.6
50 (n = 3) 100 35.8 (0.5) 100 38.1 (0.8) 2.3
25 (n = 24)b 91.6 35.8 (1.9) 95.2 37.3 (1.6) 1.5
25 (n = 18)c 100 35.9 (2.1) 100 37.1 (1.7) 1.2
5 (n = 10)b 80.0 36.8 (0.6) 80.0 38.6 (1.4) 1.7
5 (n = 7)c 100 36.7 (0.5) 100 38.3 (1.2) 1.6
a

Results of independent testing center.

b

Data generated when testing fresh DNA and DNA template exposed to long-term storage.

c

Data generated when testing fresh DNA template only.

d

n, number of biological replicates tested at each burden. More replicates were tested at the lower burdens as, on the basis of published Cq values, these represent clinically encountered burdens.