IL-1 β secretion induced by Aggregatibacter ( Actinobacillus) actinomycetemcomitans is mainly caused by the leukotoxin

Abstract

Aggregatibacter ( Actinobacillus) actinomycetemcomitans forms a leukotoxin that selectively lyses primate neutrophils, monocytes and triggers apoptosis in promyeloic cells and degranulation of human neutrophils. Recently, we showed that the leukotoxin causes activation of caspase-1 and abundant secretion of bio-active IL-1 β from human macrophages. In this study, we show that high levels of IL- β correlated with a high proportion of A. actinomycetemcomitans in clinical samples from a patient with aggressive periodontitis. To determine the relative contribution of leukotoxin to the overall bacteria-induced IL-1 β secretion, macrophages were isolated from peripheral blood and exposed to different concentrations of live A. actinomycetemcomitans strains with either no, low or high production of leukotoxin. Cell lysis and levels of IL-1 β, IL-6, TNF- α and caspase-1 were measured by ELISA and flow cytometry. Leukotoxin was the predominant cause of IL-1 β secretion from macrophages, even in the A. actinomycetemcomitans strain with low leukotoxin production. Macrophages exposed to non-leukotoxic bacteria accumulated cytosolic pro-IL-1 β, which was secreted by a secondary exposure to leukotoxic bacteria. In conclusion, the present study shows for the first time that A. actinomycetemcomitans-induced IL-1 β secretion from human macrophages in vitro is mainly caused by leukotoxin.