TABLE 4.
Bacterial strain and treatment | Colony countb
|
Pc | |||
---|---|---|---|---|---|
Mean
|
SE
|
||||
24 h | 5 days | 24 h | 5 days | ||
BCG | |||||
None | 1,238 | 2,847 | 304.9 | 688.2 | 0.1800 |
IFN-γ + LPS | 987 | 287 | 286.4 | 58.4 | 0.0459 |
DPP | |||||
None | 2,154 | 6,573 | 338.59 | 823 | 0.0003 |
IFN-γ + LPS | 1,093 | 2,557 | 327.15 | 684.8 | 0.033 |
Thioglycolate (3%) was injected into the peritoneal cavities of iNOS−/− mice. Four days after injection, animals were anesthetized with Isoflurane. Peritoneal cavities were washed with ice-cold RPMI to recover peritoneal macrophages. Peritoneal macrophages were infected with BCG or DPP at an MOI of 10:1. At 2 h after infection, unphagocytosed organisms were removed. BCG- or DPP-infected macrophages were maintained in RPMI containing 10% fetal bovine serum or in RPMI containing 10% fetal bovine serum, IFN-γ (100 U/ml), and LPS (1 μg/ml).
Intracellular colony counts were determined by plating lysed cultures on Middlebrook 7H11. Results are averages from three experiments done in triplicate.
Calculated with the Statview program.