Chemistry and Structural Biology Department, Institut Pasteur, UMR CNRS 3528, CEDEX 15, 75724 Paris, France.
Université Paris Diderot Paris VII, 75013 Paris, France.
Toxins (Basel). 2019 Feb 13;11(2):111. doi: 10.3390/toxins11020111.
The adenylate cyclase (CyaA) toxin produced in is the causative agent of whooping cough. CyaA exhibits the remarkable capacity to translocate its N-terminal adenyl cyclase domain (ACD) directly across the plasma membrane into the cytosol of eukaryotic cells. Once translocated, calmodulin binds and activates ACD, leading to a burst of cAMP that intoxicates the target cell. Previously, Gonzalez-Bullon et al. reported that CyaA exhibits a phospholipase A activity that could destabilize the membrane to facilitate ACD membrane translocation. However, Bumba and collaborators lately reported that they could not replicate these results. To clarify this controversy, we assayed the putative PLA activity of two CyaA samples purified in two different laboratories by using two distinct fluorescent probes reporting either PLA2 or both PLA1 and PLA2 activities, as well as in various experimental conditions (i.e., neutral or negatively charged membranes in different buffers.) However, we could not detect any PLA activity in these CyaA batches. Thus, our data independently confirm that CyaA does not possess any PLA activity.
在 中产生的腺苷酸环化酶(CyaA)毒素是百日咳的病原体。CyaA 具有将其 N 端腺苷酸环化酶结构域(ACD)直接穿过质膜转运到真核细胞质中的显著能力。一旦转运,钙调蛋白结合并激活 ACD,导致 cAMP 的爆发,使靶细胞中毒。先前,Gonzalez-Bullon 等人报告说,CyaA 表现出一种可能破坏膜的磷脂酶 A 活性,以促进 ACD 膜转运。然而,Bumba 和合作者最近报告说,他们无法复制这些结果。为了解决这一争议,我们使用两种不同的荧光探针检测了在两个不同实验室中纯化的两种 CyaA 样本的假定 PLA 活性,这两种探针分别报告 PLA2 或 PLA1 和 PLA2 的活性,以及在各种实验条件下(即在不同缓冲液中的中性或带负电荷的膜)。然而,我们在这些 CyaA 批次中未检测到任何 PLA 活性。因此,我们的数据独立证实 CyaA 不具有任何 PLA 活性。