Department of Pathogen Biology, School of Public Health, Southern Medical University, Guangzhou, Guangdong, China.
Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA.
J Exp Med. 2020 Mar 2;217(3). doi: 10.1084/jem.20181757.
The ability of Toxoplasma gondii to inject the rhoptry kinase ROP16 into host cells results in the activation of the transcription factors STAT3 and STAT6, but it is unclear how these events impact infection. Here, parasites that inject Cre-recombinase with rhoptry proteins were used to distinguish infected macrophages from those only injected with parasite proteins. Transcriptional profiling revealed that injection of rhoptry proteins alone was sufficient to induce an M2 phenotype that is dependent on STAT3 and STAT6, but only infected cells displayed reduced expression of genes associated with antimicrobial activity and protective immunity. In vivo, the absence of STAT3 or STAT6 improved parasite control, while the loss of ROP16 resulted in a marked reduction in parasite numbers and heightened parasite-specific T cell responses. Thus, ROP16 is a virulence factor that can act in cis and trans to promote M2 programs and which limits the magnitude of parasite-specific T cell responses.
刚地弓形虫将其rhoptry 激酶 ROP16 注入宿主细胞的能力导致转录因子 STAT3 和 STAT6 的激活,但这些事件如何影响感染尚不清楚。在这里,使用注入 rhoptry 蛋白和 Cre 重组酶的寄生虫将感染的巨噬细胞与仅注射寄生虫蛋白的巨噬细胞区分开来。转录谱分析显示,单独注射 rhoptry 蛋白足以诱导依赖于 STAT3 和 STAT6 的 M2 表型,但只有感染细胞显示与抗菌活性和保护性免疫相关的基因表达降低。在体内,STAT3 或 STAT6 的缺失改善了寄生虫的控制,而 ROP16 的缺失导致寄生虫数量明显减少和寄生虫特异性 T 细胞反应增强。因此,ROP16 是一种毒力因子,它可以顺式和反式起作用,促进 M2 程序,并限制寄生虫特异性 T 细胞反应的幅度。