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. 2020 Nov 17;6(4):292. doi: 10.3390/jof6040292

Table 3.

Detection of P. jirovecii in clinical samples using the reference method (PCR) and S2 material. Each sample was analyzed by triplicate.

Sample a Biological Fluid Reference Method (PCR) b S2 c
Ct Result Result
1 Sputum 28 Infected +
2 Sputum 27.5 Infected +
3 BAL 36.6 Infected +
4 Sputum 28.5 Infected +
5 BAL 38.8 Infected +
6 BAL 19 Infected +
7 Sputum 26.8 Infected +
8 Sputum 30.28 Infected +
9 Sputum 35.3 Infected +
10 Sputum 34.9 Infected +
11 BAL > 40 Non-Infected -
12 Sputum > 40 Non-Infected -
13 NPA - Non- Infected -
14 NPA - Non- Infected -
15 NPA - Non- Infected -
16 NPA 33.6 Infected +
17 NPA 37.2 Infected +
18 NPA 34.9 Infected +
19 NPA 28.8 Infected +
20 NPA - Non- Infected -
21 NPA 33.4 Infected +
22 NPA - Non- Infected -
23 NPA - Non- Infected -
24 NPA - Non- Infected -
25 NPA - Non- Infected +
26 NPA - Non- Infected +
27 NPA - Non- Infected -
28 NPA 34.9 Infected -
29 NPA 39.4 Infected -
30 NPA 34.4 Infected +
31 NPA 34.6 Infected +
32 NPA 33.4 Infected +
33 NPA 35.5 Infected -

a Samples 1 to 12 were from patients of Hospital Universitari i Politècnic La Fe and samples 13 to 33 were from newborn infant patients of Hospital Universitario Virgen del Rocío. b Samples were considered positives (+) when two different aliquots of each patient were positive by specific PCR for P. jirovecii. c Samples were considered positives (+) when the fluorescence signal at 585 nm (λexc = 555 nm) was higher than the average fluorescence of the negative controls plus three times the standard deviation.