Bernhard Nocht Institute for Tropical Medicine, Dept. Infectious Disease Epidemiology, Hamburg, Germany.
Immunobiology Infection Unit, Institut Pasteur, INSERM U1221, Paris, France.
PLoS Negl Trop Dis. 2020 Oct 2;14(10):e0008709. doi: 10.1371/journal.pntd.0008709. eCollection 2020 Oct.
Mycobacterium ulcerans is a human pathogen that causes a necrotizing skin disease known as Buruli ulcer. Necrosis of infected skin is driven by bacterial production of mycolactone, a diffusible exotoxin targeting the host translocon (Sec61). By blocking Sec61, mycolactone prevents the transport of nascent secretory proteins into the endoplasmic reticulum of host cells. This triggers pro-apoptotic stress responses partially depending on activation of the ATF4 transcription factor. To gain further insight into the molecular pathways mediating the cytotoxic effects of mycolactone we conducted the first haploid genetic screen with the M. ulcerans toxin in KBM-7 cells. This approach allowed us to identify the histone methyltransferase SETD1B as a novel mediator of mycolactone-induced cell death. CRISPR/Cas9-based inactivation of SETD1B rendered cells resistant to lethal doses of the toxin, highlighting the critical importance of this gene's expression. To understand how SETD1B contributes to mycolactone cytotoxicity, we compared the transcriptomes of wild-type (WT) and SETD1B knockout KBM-7 cells upon exposure to the toxin. While ATF4 effectors were upregulated by mycolactone in both WT and SETD1B knockout cells, mycolactone selectively induced the expression of pro-apoptotic genes in WT cells. Among those genes we identified CHAC1, which codes for a major glutathione (GSH)-degrading enzyme, and whose strong upregulation in mycolactone-treated WT cells correlated with a marked reduction in GSH protein level. Moreover, GSH supplementation conferred cells with substantial protection against the toxic effects of mycolactone. Our data thus identify SETD1B/CHAC1/GSH as a novel, epigenetic mechanism connecting Sec61 blockade with apoptotic cell death. They suggest that GSH-based treatments might have the capacity to limit skin necrosis in Buruli ulcer.
溃疡分枝杆菌是一种人类病原体,可引起一种称为布鲁里溃疡的坏死性皮肤疾病。感染皮肤的坏死是由细菌产生的(mycolactone)引起的,mycolactone 是一种扩散的外毒素,靶向宿主易位体(Sec61)。通过阻断 Sec61,mycolactone 阻止新生分泌蛋白向宿主细胞的内质网转运。这会触发部分依赖于 ATF4 转录因子激活的促凋亡应激反应。为了更深入地了解介导(mycolactone)细胞毒性作用的分子途径,我们首次在 KBM-7 细胞中进行了与 M.溃疡毒素的单倍体遗传筛选。这种方法使我们能够识别组蛋白甲基转移酶 SETD1B 作为(mycolactone)诱导细胞死亡的新型介质。基于 CRISPR/Cas9 的 SETD1B 失活使细胞对毒素的致死剂量具有抗性,突出了该基因表达的关键重要性。为了了解 SETD1B 如何促进(mycolactone)细胞毒性,我们比较了暴露于毒素后的野生型(WT)和 SETD1B 敲除 KBM-7 细胞的转录组。虽然 ATF4 效应物在 WT 和 SETD1B 敲除细胞中均被(mycolactone)上调,但(mycolactone)选择性地诱导 WT 细胞中促凋亡基因的表达。在这些基因中,我们鉴定出 CHAC1,它编码一种主要的谷胱甘肽(GSH)-降解酶,其在(mycolactone)处理的 WT 细胞中的强烈上调与 GSH 蛋白水平的显著降低相关。此外,GSH 补充赋予细胞对(mycolactone)毒性作用的显著保护。因此,我们的数据确定 SETD1B/CHAC1/GSH 作为连接 Sec61 阻断与细胞凋亡死亡的新型表观遗传机制。它们表明基于 GSH 的治疗方法可能有能力限制布鲁里溃疡中的皮肤坏死。