TABLE 4.
Effectiveness of DNase in elimination of nonviable Vibrio cells prior to DNA extraction
| Strain | Treatment | No. of CFU g−1
|
DNA concn (ng μl−1)a | ΔRQ valueb | |
|---|---|---|---|---|---|
| Initial | Final | ||||
| V. cholerae O1 (ATCC 14035) | None | 7.2 × 107 | 6.5 × 107 | 108 | 35.2 |
| 111 | 35.4 | ||||
| 105 | 35.8 | ||||
| DNase | 7.2 × 107 | 6.2 × 106 | 90 | 37.5 | |
| 92 | 37.8 | ||||
| 89 | 37.0 | ||||
| V. cholerae O139 (ATCC 51394) | None | 6.4 × 107 | 5.8 × 107 | 100 | 35.2 |
| 104 | 35.5 | ||||
| 96 | 35.4 | ||||
| DNase | 6.4 × 107 | 5.3 × 106 | 89 | 37.0 | |
| 91 | 37.2 | ||||
| 87 | 37.4 | ||||
DNA was amplified with the hlyA TaqMan primers in the presence of the hlyA fluorogenic probe. The values shown are from three separate experiments. The DNA samples were analyzed in triplicate for each PCR.
Positive values were assigned when the ΔRQ was greater than the ΔRQ threshold value, based on the average value of the no-template controls (n = 4). ΔRQ values are the arithmetic mean of the triplicate DNA samples in each PCR analysis.