牛巴贝斯虫球形体蛋白 3 在受感染红细胞脊形成过程中的关键作用。

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2024-11-11 eCollection Date: 2024-11-01 DOI:10.1371/journal.ppat.1012294
Atefeh Fathi, Hassan Hakimi, Miako Sakaguchi, Junya Yamagishi, Shin-Ichiro Kawazu, Masahito Asada
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引用次数: 0

摘要

牛巴贝斯虫(Babesia bovis)是一种红细胞内原生动物寄生虫,给世界各地的养牛业造成了严重的经济损失。感染这种寄生虫后,受感染的红细胞(iRBC)会在大脑微血管中积聚,导致严重的临床并发症,即脑巴贝西亚原虫病。寄生虫在 iRBC 生长过程中会向 iRBC 输出各种蛋白质,从而在 iRBC 表面形成被称为 "脊 "的突起,作为细胞粘附到内皮细胞的部位。球形体蛋白质(SBPs;从球形体分泌的蛋白质,球形体是螺浆虫特有的细胞器)被导出到 iRBC 中,迄今已报道了四种蛋白质(SBP1-4)。在本研究中,我们利用诱导基因敲除(KD)系统阐明了 SBP3 的功能。通过免疫荧光检测评估了 SBP3 的定位,结果发现 SBP3 和 SBP4 在 iRBCs 内只有部分共定位。相反,却观察到了与 VESA-1 的共定位,VESA-1 是负责细胞粘附的主要寄生虫配体。免疫电镜证实了 SBP3 在脊上的定位。利用 glmS 系统对 SBP3 进行了 KD,并通过 Western 印迹、免疫荧光检测和 RNA-seq 分析证实了有效的 KD。SBP3 KD 寄生虫表现出严重的生长缺陷,这表明它对寄生虫在 iRBCs 中的存活非常重要。在 SBP3 KD 寄生虫中几乎检测不到 iRBC 表面的 VESA-1,而 iRBC 中仍然检测到 SBP4。此外,在 SBP3 KD 寄生虫中观察到 iRBC 上的脊消失,iRBC 对牛脑内皮细胞的细胞粘附减少。免疫沉淀后的质谱分析检测到宿主 Band 3 多蛋白复合物,表明 SBP3 与 iRBC 细胞骨架蛋白有关联。综上所述,本研究揭示了 SBP3 在脊形成中的重要作用及其在脑巴贝西亚原虫病发病机制中的重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Critical role of Babesia bovis spherical body protein 3 in ridge formation on infected red blood cells.

Babesia bovis, an apicomplexan intraerythrocytic protozoan parasite, causes serious economic loss to cattle industries around the world. Infection with this parasite leads to accumulation of infected red blood cells (iRBCs) in the brain microvasculature that results in severe clinical complications known as cerebral babesiosis. Throughout its growth within iRBCs, the parasite exports various proteins to the iRBCs that lead to the formation of protrusions known as "ridges" on the surface of iRBCs, which serve as sites for cytoadhesion to endothelial cells. Spherical body proteins (SBPs; proteins secreted from spherical bodies, which are organelles specific to Piroplasmida) are exported into iRBCs, and four proteins (SBP1-4) have been reported to date. In this study, we elucidated the function of SBP3 using an inducible gene knockdown (KD) system. Localization of SBP3 was assessed by immunofluorescence assay, and only partial colocalization was detected between SBP3 and SBP4 inside the iRBCs. In contrast, colocalization was observed with VESA-1, which is a major parasite ligand responsible for the cytoadhesion. Immunoelectron microscopy confirmed localization of SBP3 at the ridges. SBP3 KD was performed using the glmS system, and effective KD was confirmed by Western blotting, immunofluorescence assay, and RNA-seq analysis. The SBP3 KD parasites showed severe growth defect suggesting its importance for parasite survival in the iRBCs. VESA-1 on the surface of iRBCs was scarcely detected in SBP3 KD parasites, whereas SBP4 was still detected in the iRBCs. Moreover, abolition of ridges on the iRBCs and reduction of iRBCs cytoadhesion to the bovine brain endothelial cells were observed in SBP3 KD parasites. Immunoprecipitation followed by mass spectrometry analysis detected the host Band 3 multiprotein complex, suggesting an association of SBP3 with iRBC cytoskeleton proteins. Taken together, this study revealed the vital role of SBP3 in ridge formation and its significance in the pathogenesis of cerebral babesiosis.

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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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