TABLE 6.
Detection of V. parahaemolyticus in seeded oysters with overnight enrichmenta
| Amt of V. parahaemolyticus seeded (CFU) | Final V. parahamolyticus concn (109 CFU/ml)b |
Ct value
|
|||
|---|---|---|---|---|---|
| tlh | ORF8 | tdh | trh | ||
| 105 | 3.88 | 18.94 ± 1.38 | 17.87 ± 2.03 | 16.75 ± 1.41 | 18.18 ± 1.57 |
| 104 | 4.20 | 19.33 ± 0.85 | 19.55 ± 0.59 | 17.24 ± 0.84 | 18.57 ± 1.22 |
| 103 | 2.80 | 19.36 ± 0.75 | 24.37 ± 2.26 | 17.55 ± 0.92 | 18.16 ± 1.03 |
| 102 | 4.65 | 20.08 ± 0.49 | 19.02 ± 0.97 | 17.40 ± 0.70 | 19.54 ± 0.93 |
| 101 | 4.00 | 19.55 ± 0.67 | 18.38 ± 0.86 | 17.18 ± 0.88 | 19.56 ± 1.31 |
| 100 | 3.30 | 20.84 ± 0.93 | 19.71 ± 0.50 | 18.61 ± 0.95 | 19.21 ± 1.44 |
| 0 | NDc | NDc | ND | ND | ND |
| Positive controld | 18.98 ± 0.42 | 18.16 ± 0.40 | 17.23 ± 0.40 | 19.29 ± 0.41 | |
| Negative controle | ND | ND | ND | ND | |
The data are means ± standard deviations for four independent experiments.
The viable plate count is an average for three dilutions.
ND, not detected.
The positive amplification control included 100 ng purified V. parahaemolyticus genomic DNA.
The negative amplification control included 3 μl sterile water.