Eby Joshua C, Gray Mary C, Hewlett Erik L
Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA
Division of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Infect Immun. 2014 Dec;82(12):5256-69. doi: 10.1128/IAI.02487-14. Epub 2014 Oct 6.
The adenylate cyclase toxin (ACT) of Bordetella pertussis intoxicates target cells by generating supraphysiologic levels of intracellular cyclic AMP (cAMP). Since ACT kills macrophages rapidly and potently, we asked whether ACT would also kill neutrophils. In fact, ACT prolongs the neutrophil life span by inhibiting constitutive apoptosis and preventing apoptosis induced by exposure to live B. pertussis. Imaging of B. pertussis-exposed neutrophils revealed that B. pertussis lacking ACT induces formation of neutrophil extracellular traps (NETs), whereas wild-type B. pertussis does not, suggesting that ACT suppresses NET formation. Indeed, ACT inhibits formation of NETs by generating cAMP and consequently inhibiting the oxidative burst. Convalescent-phase serum from humans following clinical pertussis blocks the ACT-mediated suppression of NET formation. These studies provide novel insight into the phagocyte impotence caused by ACT, which not only impairs neutrophil function but also inhibits death of neutrophils by apoptosis and NETosis.
百日咳博德特氏菌的腺苷酸环化酶毒素(ACT)通过产生超生理水平的细胞内环状AMP(cAMP)使靶细胞中毒。由于ACT能迅速且有效地杀死巨噬细胞,我们不禁要问ACT是否也会杀死中性粒细胞。事实上,ACT通过抑制组成性凋亡并防止暴露于活的百日咳博德特氏菌所诱导的凋亡来延长中性粒细胞的寿命。对暴露于百日咳博德特氏菌的中性粒细胞进行成像显示,缺乏ACT的百日咳博德特氏菌会诱导中性粒细胞胞外陷阱(NETs)的形成,而野生型百日咳博德特氏菌则不会,这表明ACT会抑制NET的形成。确实,ACT通过产生cAMP并因此抑制氧化爆发来抑制NET的形成。临床百日咳患者康复期的血清可阻断ACT介导的对NET形成的抑制作用。这些研究为ACT导致的吞噬细胞功能障碍提供了新的见解,ACT不仅损害中性粒细胞功能,还通过凋亡和NETosis抑制中性粒细胞的死亡。