Department of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Department of Microbiology, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
mBio. 2020 Mar 24;11(2):e03146-19. doi: 10.1128/mBio.03146-19.
Dermonecrotic toxin (DNT) is one of the representative toxins produced by , but its role in pertussis, infection, remains unknown. In this study, we identified the T-type voltage-gated Ca channel Ca3.1 as the DNT receptor by CRISPR-Cas9-based genome-wide screening. As Ca3.1 is highly expressed in the nervous system, the neurotoxicity of DNT was examined. DNT affected cultured neural cells and caused flaccid paralysis in mice after intracerebral injection. No neurological symptoms were observed by intracerebral injection with the other major virulence factors of the organisms, pertussis toxin and adenylate cyclase toxin. These results indicate that DNT has aspects of the neurotropic virulence factor of The possibility of the involvement of DNT in encephalopathy, which is a complication of pertussis, is also discussed., which causes pertussis, a contagious respiratory disease, produces three major protein toxins, pertussis toxin, adenylate cyclase toxin, and dermonecrotic toxin (DNT), for which molecular actions have been elucidated. The former two toxins are known to be involved in the emergence of some clinical symptoms and/or contribute to the establishment of bacterial infection. In contrast, the role of DNT in pertussis remains unclear. Our study shows that DNT affects neural cells through specific binding to the T-type voltage-gated Ca channel that is highly expressed in the central nervous system and leads to neurological disorders in mice after intracerebral injection. These data raise the possibility of DNT as an etiological agent for pertussis encephalopathy, a severe complication of infection.
无细胞坏死毒素(DNT)是 产生的代表性毒素之一,但它在百日咳、感染中的作用尚不清楚。在这项研究中,我们通过基于 CRISPR-Cas9 的全基因组筛选鉴定出 T 型电压门控钙通道 Ca3.1 为 DNT 受体。由于 Ca3.1 在神经系统中高度表达,因此研究了 DNT 的神经毒性。DNT 影响培养的神经细胞,并在脑内注射后导致小鼠弛缓性瘫痪。脑内注射该生物体的其他主要毒力因子,如百日咳毒素和腺苷酸环化酶毒素,则没有观察到神经症状。这些结果表明 DNT 具有 的神经毒性毒力因子的某些方面。还讨论了 DNT 是否参与百日咳的脑病并发症,这是百日咳的一种并发症。引起百日咳的传染性呼吸道疾病产生三种主要的蛋白毒素,即百日咳毒素、腺苷酸环化酶毒素和无细胞坏死毒素(DNT),其分子作用已被阐明。前两种毒素已知与一些临床症状的出现有关,或有助于细菌感染的建立。相比之下,DNT 在百日咳中的作用尚不清楚。我们的研究表明,DNT 通过与在中枢神经系统中高度表达的 T 型电压门控钙通道特异性结合来影响神经细胞,并在脑内注射后导致小鼠出现神经紊乱。这些数据提出了 DNT 作为百日咳脑病的病因的可能性,这是 感染的一种严重并发症。