[刚地弓形虫入侵宿主细胞时状体蛋白16的分泌和分布]。

Shi-chen Jiang, Hai-xia Wei, Cheng He, Sheng-qun Deng, Jing Xia, Hong-juan Peng
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引用次数: 0

摘要

目的:探讨不同弓形虫侵染宿主细胞时,弓形虫虫体蛋白16 (ROP16)的分泌及定位。方法:在弓形虫RH菌株cDNA上,通过PCR扩增Tgrop16基因,亚克隆到质粒pET-32a(+)中,在异丙基β- d -1-硫代半乳糖苷诱导下,在大肠杆菌BL21(DE3)中表达。用表达的重组蛋白TgROP16免疫新西兰兔,产生抗TgROP16的多克隆抗体。分别用Western blotting和间接ELISA检测多克隆抗体的特异性和敏感性。采用real-time PCR和Western blotting分别检测弓形虫RH株和Pru株中Tgrop16的转录和蛋白水平。采用间接免疫荧光法(IFA)检测弓形虫RH株和Pru株侵袭人包皮成纤维细胞(HFFs)时TgROP16的分泌和分布。结果:Western blotting在M(r) ~10万处显示特异性条带,表明兔源性抗TgROP16多克隆抗体能够识别TgROP16。间接ELISA检测抗体滴度为1:25 600。Tgrop16在Pru株中的相对表达量[(7.786±0.206)]是RH株[(1.000±0.110)]的7倍(结论:抗Tgrop16多克隆抗体具有较高的特异性和敏感性。RH菌株的TgROP16蛋白水平高于Pru菌株。在这两种菌株中,TgROP16在入侵前定位于未招募的速殖体的顶端复合体上,在入侵过程中从招募的速殖体中分泌出来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Secretion and Distribution of Rhoptry Protein 16 during Toxoplasma gondii Invasion into Host Cells].

Objective: To examine the secretion and localization of Toxoplasma gondii Rhoptry protein 16 (ROP16) during invasion of different strains of T. gondii into host cells.

Methods: The Tgrop16 gene was amplified by PCR on the cDNA of T. gondii RH strain, subcloned into the plasmid pET-32a(+), and expressed in Escherichia coli BL21(DE3) under the induction of isopropyl β-D-1-thiogalactopyranoside. New Zealand rabbit was immuned with the expressed recombinant protein TgROP16 to produce polyclonal anti-TgROP16 antibody. The specificity and sensitivity of the polyclonal antibody were examined by Western blotting and indirect ELISA, respectively. The transcriptional and protein levels of Tgrop16 in T. gondii RH strain and Pru strain were determined by real-time PCR and Western blotting, respectively. The secretion and distribution of TgROP16 in human foreskin fibroblasts (HFFs) during the invasion by T. gondii RH strain and Pru strain were examined by indirect immunofluorescence assay (IFA).

Results: Western blotting showed a specific band at M(r) of ~100 000, indicating that the specific rabbit-derived anti-TgROP16 polyclonal antibody was capable of recognizing TgROP16. Indirect ELISA revealed a titer of 1:25 600 for the antibody. The relative expression level of Tgrop16 in Pru strain[(7.786±0.206)] was 7 times than that in RH strain[(1.000±0.110)](P<0.05) as detected by real-time PCR, and TgROP16 protein level was higher in RH strain than in Pru strain. IFA showed that TgROP16 was localized on the apical complex of the unrecruited tachyzoite of T. gondii before invasion and was secreted out of the recruited tachyzoite after invasion.

Conclusion: The anti-TgROP16 polyclonal antibody has high specificity and sensitivity. The TgROP16 protein level is higher in the RH strain than in the Pru strain. For both strains, TgROP16 is localized on the apical complex of the unrecruited tachyzoite before invasion and secreted out of the recruited tachyzoite during invasion.

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