Table 2.
Strains | Bacterial concentration before challenge (108 CFU/mL)*, † | Survival percentage (%) after challenge* | ||||||
---|---|---|---|---|---|---|---|---|
Name | Genotype | H2O2 | Polymyxin B | SDS | Phenol | CuSO4 | ZnSO4 | |
306/pUFR053 | WT | 9.33 ± 0.58a | 5.76 ± 1.19a | 14.81 ± 1.28a | 0.57 ± 0.03a | 93.51 ± 5.78a | 1.02 ± 0.42a | 1.42 ± 0.32a |
406G8/pUFR053 | nlxA− | 10.33 ± 0.85a | 0.85 ± 0.04b | 3.84 ± 1.61b | 0.07 ± 0.03b | 41.76 ± 12.61b | 0.18 ± 0.10b | 0.37 ± 0.08b |
406G8/p53‐nlxA | nlxA+ | 10.67 ± 1.53a | 10.48 ± 4.62a | 14.21 ± 2.42a | 0.42 ± 0.13a | 95.83 ± 7.22a | 1.00 ± 0.57a | 1.47 ± 0.19a |
All the experiments were repeated three times independently with four replications each time. Similar results were observed and only one representative result is presented.
For significant difference analysis, the survival percentages of four replications of each strain were calculated independently and then subjected to Student's t‐test. Data with different letters (a, b) denote significant difference (P < 0.01) between strains in the same treatment. Means and standard errors from one representative result are shown.
All strains were cultured for 20 h in nutrient broth (NB). Initial cell concentrations [colony‐forming units (CFU)/mL] were measured by diluting the bacterial cultures appropriately and plating on nutrient agar (NA) plates before challenge with different stresses. For each strain tested, similar cell concentrations were observed in different stress assays. Only one set of the representative data is shown.