Table 4.
M. avium strain | No. of c.f.u. (ml macrophage lysate)−1* | ||
---|---|---|---|
1 h | 24 h | ||
−N-MA | +N-MA | ||
WT (MAC 104) | 6.4±0.3×105 | 8.3±0.3×105 | 8.7±0.5×105 |
STM1 | 2.0±0.4×105 | 8.1±0.3×104 | 8.5±0.6×104 |
STM2 | 4.4±0.2×105 | 7.6±0.3×104 | 8.1±0.2×104 |
STM3 | 5.2±0.5×105 | 4.1±0.3×105 | 3.8±0.4×105 |
STM4 | 2.6±0.2×105 | 1.0±0.3×105 | 9.8±0.2×105 |
STM5 | 3.4±0.2×105 | 9.8±0.3×104 | 1.0±0.4×105 |
STM6 | 3.9±0.5×105 | 2.8±0.4×105 | 2.7±0.6×105 |
STM8 | 3.8±0.2×105 | 8.3±0.3×104 | 7.6±0.5×104 |
STM10 | 4.6±0.3×105 | 4.1±0.5×104 | 1.6±0.3×105† |
STM11 | 2.5±0.5×105 | 7.8±0.4×104 | 1.2±0.6×105† |
*RAW 246.7 macrophage monolayers were infected for 1 h with M. avium, washed, and all of the wells were treated with IFN-γ and with 100 μM N-methylarginine. The monolayers were lysed after 24 h and the intracellular bacteria quantified. The experiments were repeated three times.
†P<0.05 compared with the number of bacteria at 24 h without N-methylarginine.