TABLE 3.
DNA amplification by PCR or PCR-BSA in 139 samplesa
Samplea | Amplifi- cation methodb | Total no. of samples | No. of samples showing:
|
||
---|---|---|---|---|---|
T. gondii DNA absent | T. gondii DNA present | Inhibitor persistencec | |||
RSW | PCR | 16 | 13 | 3 | |
PCR-BSA | 29 | 19 | 10 | ||
UW | PCR | 32 | 26 | 6 | |
PCR-BSA | 18 | 14 | 4 | ||
PDW | PCR | 38 | 38 | ||
PCR-BSA | 6 | 5 | 1 | ||
Total | 139 | 115 | 10 | 14 |
There were 45 RSW samples, 50 UW samples, and 44 PDW samples.
The PCR-BSA method was used when inhibitors hindered standard PCR.
Persistence after BSA treatment; result uninterpretable.