Institute for Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Edinburgh, EH93FL, UK.
Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, LA1 4AT, UK.
Nat Commun. 2022 Jun 9;13(1):3322. doi: 10.1038/s41467-022-31057-1.
Trypanosomes causing African sleeping sickness use quorum-sensing (QS) to generate transmission-competent stumpy forms in mammalian hosts. This density-dependent process is signalled by oligopeptides that stimulate the signal transduction pathway leading to stumpy formation. Here, using mass spectrometry analysis, we identify peptidases released by trypanosomes and, for 12 peptidases, confirm their extracellular delivery. Thereafter, we determine the contribution of each peptidase to QS signal production using systematic inducible overexpression in vivo, and confirm this activity operates through the physiological QS signalling pathway. Gene knockout of the QS-active peptidases identifies two enzymes, oligopeptidase B and metallocarboxypeptidase 1, that significantly reduce QS when ablated individually. Further, combinatorial gene knockout of both peptidases confirms their dominance in the generation of the QS signal, with peptidase release of oligopeptidase B mediated via an unconventional protein secretion pathway. This work identifies how the QS signal driving trypanosome virulence and transmission is generated in mammalian hosts.
导致非洲昏睡病的锥体虫通过群体感应(QS)在哺乳动物宿主体内产生有传播能力的短尾形式。这种密度依赖性过程由刺激导致短尾形成的信号转导途径的寡肽信号。在这里,我们使用质谱分析鉴定了锥体虫释放的肽酶,并对 12 种肽酶进行了确认,证实它们在细胞外传递。此后,我们通过体内系统诱导过表达确定了每种肽酶对 QS 信号产生的贡献,并证实该活性通过生理 QS 信号通路起作用。QS 活性肽酶的基因敲除鉴定出两种酶,即寡肽酶 B 和金属羧肽酶 1,当它们单独缺失时,QS 活性显著降低。此外,这两种肽酶的组合基因敲除证实了它们在 QS 信号生成中的主导地位,寡肽酶 B 的肽酶释放通过一种非传统的蛋白质分泌途径介导。这项工作确定了在哺乳动物宿主中驱动锥体虫毒力和传播的 QS 信号是如何产生的。