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荚膜样层中 EsxA 的保留与细胞毒性有关,并可被肺表面活性剂所拮抗。

Retention of EsxA in the Capsule-Like Layer of Is Associated with Cytotoxicity and Is Counteracted by Lung Surfactant.

机构信息

Division of Microbiology and Molecular Medicine, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden.

Division of Nanoscopy, The Maastricht Multimodal Molecular Imaging Institute, Maastricht University, Maastricht, The Netherlands.

出版信息

Infect Immun. 2019 Feb 21;87(3). doi: 10.1128/IAI.00803-18. Print 2019 Mar.

Abstract

, the pathogen that causes tuberculosis, primarily infects macrophages but withstands the host cell's bactericidal effects. EsxA, also called virulence factor 6-kDa early secretory antigenic target (ESAT-6), is involved in phagosomal rupture and cell death. We provide confocal and electron microscopy data showing that bacteria grown without detergent retain EsxA on their surface. Lung surfactant has detergent-like properties and effectively strips off this surface-associated EsxA, which advocates a novel mechanism of lung surfactant-mediated defense against pathogens. Upon challenge of human macrophages with these bacilli, the amount of surface-associated EsxA rapidly declines in a phagocytosis-independent manner. Furthermore, bacteria cultivated under exclusion of detergent exert potent cytotoxic activity associated with bacterial growth. Together, this study suggests that the surface retention of EsxA contributes to the cytotoxicity of and highlights how cultivation conditions affect the experimental outcome.

摘要

结核分枝杆菌是导致肺结核的病原体,主要感染巨噬细胞,但能抵抗宿主细胞的杀菌作用。EsxA,也称为毒力因子 6kDa 早期分泌抗原靶标(ESAT-6),参与吞噬体破裂和细胞死亡。我们提供共聚焦和电子显微镜数据,表明在没有去污剂的情况下生长的细菌在其表面保留 EsxA。肺表面活性剂具有去污剂样特性,可有效去除表面相关的 EsxA,这为肺表面活性剂介导的防御病原体的新机制提供了依据。在人巨噬细胞受到这些结核分枝杆菌的挑战时,表面相关的 EsxA 数量迅速以吞噬作用无关的方式下降。此外,在排除去污剂的情况下培养的细菌会产生与细菌生长相关的强烈细胞毒性活性。总之,这项研究表明 EsxA 的表面保留有助于结核分枝杆菌的细胞毒性,并强调了培养条件如何影响实验结果。

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