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. 2010 Jan;59(Pt 1):8–16. doi: 10.1099/jmm.0.012864-0

Table 4.

Susceptibility of M. avium clones to the effect of nitric oxide

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.