Internalization and phagosome escape required for Francisella to induce human monocyte IL-1β processing and release

Macrophage responses to Francisella infection have been characterized previously by subdued proinflammatory responses; however, these studies have generally focused on macrophage cell lines or monocyte-derived macrophages. Therefore, we studied the ability of fresh human blood monocytes to engulf and respond to Franciselia by using the live vaccine strain variant and Francisella novicida. Because Francisella organisms have been reported to escape from the phagolysosome into the cytosol, we hypothesized that this escape may trigger the activation of caspase-1. Franciselia tularensis variants were readily taken up by fresh human CD14+ monocytes, inducing the release of IL-1 beta, as well as IL-8, in a time-and dose-dependent fashion. importantly, whereas live and dead Escherichia coli, F. novicida, and live vaccine strain, as well as the LPS of E. coli, were able to induce abundant IL-1 beta mRNA synthesis and intracellular pro-IL-1 beta production, only live Francisella induced enhanced IL-1 beta processing and release (51 +/- 10 vs. 7.1 +/- 2.1 ng/ml, for F. novicida vs. E. coli LPS; P = 0.0032). Cytochalasin D blocked the Franciselia internalization and the Francisella-induced monocyte IL-1 beta processing and release but not that induced by the exogenous stimulus E coli LIPS. Also, killing bacteria did not block uptake but significantly diminished the IL-1 beta processing and release that was induced by Franciselial. Blocking bacterial escape from the phagosome into the cytosol also decreased IL-1 beta but not IL-8 release. These findings demonstrate that Francisella organisms efficiently induce IL-1 beta processing and release in fresh monocytes by means of a sensing system that requires the uptake of live bacteria capable of phagosome escape.