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环形泰勒虫 SVSP455 与宿主 HSP60 相互作用。

Theileria annulata SVSP455 interacts with host HSP60.

机构信息

State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute-Chinese Academy of Agricultural Science, Xujiaping 1, Lanzhou, Gansu, 730046, People's Republic of China.

Qinghai Academy of Animal Sciences and Veterinary Medicine, Qinghai University, Xining, Qinghai, 810016, People's Republic of China.

出版信息

Parasit Vectors. 2022 Aug 30;15(1):308. doi: 10.1186/s13071-022-05427-z.

Abstract

BACKGROUND

Theileria annulata, a transforming parasite, invades bovine B cells, dendritic cells and macrophages, promoting the uncontrolled proliferation of these cells. This protozoan evolved intricate strategies to subvert host cell signaling pathways related to antiapoptotic signaling to enable survival and proliferation within the host cells. However, the molecular mechanisms of the cell transformation induced by T. annulata remain largely unclear. Although some studies have predicted that the subtelomere-encoded variable secreted protein (SVSP) family plays roles in host-parasite interactions, the evidence for this is limited.

METHODS

In the present study, the SVSP455 (TA05545) gene, a member of the SVSP gene family, was used as the target molecule. The expression pattern of SVSP455 in different life-cycle stages of T. annulata infection was explored using a quantitative real-time PCR assay, and the subcellular distribution of SVSP455 was observed using confocal microscopy. The host cell proteins interacting with SVSP455 were screened using the Y2H system, and their interactions were verified in vivo and in vitro using both bimolecular fluorescence complementation and confocal microscopy, and co-immunoprecipitation assays. The role played by SVSP455 in cell transformation was further explored by using overexpression, RNA interference and drug treatment experiments.

RESULTS

The highest level of the SVSP455 transcript was detected in the schizont stage of T. annulata, and the protein was located both on the surface of schizonts and in the host cell cytoplasm. In addition, the interaction between SVSP455 and heat shock protein 60 was shown in vitro, and their link may regulate host cell apoptosis in T. annulata-infected cells.

CONCLUSION

Our findings are the first to reveal that T. annulata-secreted SVSP455 molecule directly interacts with both exogenous and endogenous bovine HSP60 protein, and that the interaction of SVSP455-HSP60 may manipulate the host cell apoptosis signaling pathway. These results provide insights into cancer-like phenotypes underlying Theilera transformation and therapeutics for protection against other pathogens.

摘要

背景

环形泰勒虫是一种转化寄生虫,可入侵牛的 B 细胞、树突状细胞和巨噬细胞,促进这些细胞的不受控制增殖。这种原生动物进化出了复杂的策略,颠覆了与抗凋亡信号相关的宿主细胞信号通路,使其能够在宿主细胞内存活和增殖。然而,环形泰勒虫引起的细胞转化的分子机制在很大程度上仍不清楚。虽然一些研究预测,端粒外编码的可变分泌蛋白(SVSP)家族在宿主-寄生虫相互作用中发挥作用,但证据有限。

方法

本研究以 SVSP 基因家族的成员 SVSP455(TA05545)基因为靶分子。采用实时荧光定量 PCR 检测方法研究 SVSP455 在环形泰勒虫感染不同生活史阶段的表达模式,并用共聚焦显微镜观察 SVSP455 的亚细胞分布。利用 Y2H 系统筛选与 SVSP455 相互作用的宿主细胞蛋白,并通过体内和体外的双分子荧光互补和共聚焦显微镜及免疫共沉淀实验验证其相互作用。利用过表达、RNA 干扰和药物处理实验进一步探讨 SVSP455 在细胞转化中的作用。

结果

SVSP455 转录本在环形泰勒虫裂殖体阶段表达水平最高,蛋白定位于裂殖体表面和宿主细胞质中。此外,体外实验证实 SVSP455 与热休克蛋白 60 相互作用,它们的相互作用可能调节环形泰勒虫感染细胞中的宿主细胞凋亡。

结论

本研究首次揭示环形泰勒虫分泌的 SVSP455 分子直接与外源性和内源性牛 HSP60 蛋白相互作用,SVSP455-HSP60 相互作用可能调控宿主细胞凋亡信号通路。这些结果为环形泰勒虫转化的癌症样表型及其对其他病原体的保护治疗提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a4/9426020/57e8f231ca6b/13071_2022_5427_Fig1_HTML.jpg

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