TABLE 3.
In vitro survival of BCG and DPP in murine peritoneal macrophages from wild-type mice, with and without IFN-γ plus LPSa
Bacterial strain and treatment | Colony countb
|
Pc | |||
---|---|---|---|---|---|
Mean
|
SE
|
||||
24 h | 5 days | 24 h | 5 days | ||
BCG | |||||
None | 1,196 | 407 | 285 | 52.76 | 0.088 |
IFN-γ + LPS | 1,088 | 235 | 289 | 68.5 | 0.0064 |
DPP | |||||
None | 1,670 | 13,189 | 184.29 | 461.5 | 0.0001 |
IFN-γ + LPS | 3,371 | 9,948 | 552 | 382 | 0.006 |
Thioglycolate (3%) was injected into the peritoneal cavities of wild-type C57BL/6 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. 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. Data are averages from three experiments.
Calculated with the Statview program.