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犬新孢子虫GRA6/GRA7在MDBK细胞中的鉴定与特性分析

Identification and characterization of GRA6/GRA7 of Neospora caninum in MDBK cells.

作者信息

Dong Jingquan, Li Jianhua, Wang Jinpeng, Li Fei, Yang Ju, Gong Pengtao, Li He, Zhang Xichen

机构信息

College of Veterinary Medicine, Jilin University, Changchun 130062, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2017 Apr 1;49(4):361-366. doi: 10.1093/abbs/gmx010.

Abstract

Neospora caninum, an apicomplexan parasite, is recognized as a major bovine abortifacient. Dense granule antigens (GRAs) play important roles in the formation and modification of parasitophorous vacuoles (PVs) in Toxoplasma gondii. However, a few studies investigating GRAs have been reported in N. caninum. The aim of the present study was to characterize the dense GRA6/GRA7 of N. caninum in PVs using MDBK cells as a host cell model. Neospora caninum was inoculated into MDBK cells, and changes were observed using a transmission electron microscope (TEM). Neospora caninum GRA6/GRA7 were identified and characterized using bioinformatics, cell fractionation, and immunofluorescence. The TEM results revealed that integrated PVs were present in MDBK cells after N. caninum infection. Bioinformatics analysis showed that NcGRA6/NcGRA7 shared 28.76% and 29.66% homology with T. gondii GRA6/GRA7 (TgGRA6/TgGRA7) but had similar signal peptides, transmembrane domains, and motifs. Cell fractionation and subcellular localization analyses both showed that NcGRA6 was distributed in the lumen and intravacuolar network in soluble and transmembrane forms. The transmembrane form of NcGRA7 was observed in the PV membrane. These data lay a foundation for further study on bovine neosporosis and NcGRA6/NcGRA7 function during PV formation.

摘要

犬新孢子虫是一种顶复门寄生虫,被认为是牛流产的主要病因。致密颗粒抗原(GRAs)在刚地弓形虫的寄生泡(PVs)形成和修饰过程中发挥重要作用。然而,关于犬新孢子虫GRAs的研究报道较少。本研究的目的是以MDBK细胞为宿主细胞模型,对犬新孢子虫在PVs中的致密GRA6/GRA7进行表征。将犬新孢子虫接种到MDBK细胞中,并用透射电子显微镜(TEM)观察其变化。利用生物信息学、细胞分级分离和免疫荧光技术对犬新孢子虫GRA6/GRA7进行鉴定和表征。TEM结果显示,犬新孢子虫感染后MDBK细胞中存在完整的PVs。生物信息学分析表明,犬新孢子虫NcGRA6/NcGRA7与刚地弓形虫GRA6/GRA7(TgGRA6/TgGRA7)的同源性分别为28.76%和29.66%,但具有相似的信号肽、跨膜结构域和基序。细胞分级分离和亚细胞定位分析均表明,NcGRA6以可溶性和跨膜形式分布于寄生泡腔和泡内网络中。在PV膜中观察到NcGRA7的跨膜形式。这些数据为进一步研究牛新孢子虫病以及NcGRA6/NcGRA7在PV形成过程中的功能奠定了基础。

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