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肥胖带绦虫的瞬时转基因

Transient transgenesis of the tapeworm Taenia crassiceps.

作者信息

Moguel Bárbara, Moreno-Mendoza Norma, Bobes Raúl J, Carrero Julio C, Chimal-Monroy Jesús, Díaz-Hernández Martha E, Herrera-Estrella Luis, Laclette Juan P

机构信息

Institute for Biomedical Research, Universidad Nacional Autónoma de México, Av. Universidad 3000, Coyoacán, C.P. 04510 México DF, México.

National Laboratory of Genomics for Biodiversity-cinvestav, Km 9.6 Libramiento Norte Carretera Irapuato-León, C.P. 36821 Irapuato, Gto México.

出版信息

Springerplus. 2015 Sep 15;4:496. doi: 10.1186/s40064-015-1278-y. eCollection 2015.

Abstract

Human and porcine cysticercosis is caused by the larval stage of the flatworm Taenia solium (Cestoda). Infestation of the human brain, also known as neurocysticercosis, is the most common parasite disease of the central nervous system worldwide. Significant advances in the understanding of the disease have been achieved using the Taenia crassiceps murine model. We describe here a successful transfection protocol of T. crassiceps cysticerci as the first step to approach a number of currently inaccessible biological questions on cysticercosis. T. crassiceps cysticerci (ORF strain) were microinjected with the plasmid pcDNA3.1/NT-GFP-TOPO, encoding the green fluorescent protein (GFP) driven by a cytomegalovirus promoter (CMV). Twelve hours after the microinjection, GFP fluorescence gradually developed in patches associated to bud structures in the bladder wall of cysts. Fluorescence reached a peak at 24-48 h and lasted up to 72 h after the microinjection. Immunohistochemical studies on tissue sections of transfected cysts using an anti-GFP antibody, demonstrated co-localization of the antibody and the GFP fluorescence in the tegumentary cytoplasm and subtegumentary cytons. To validate at the mRNA level the expression of GFP, we carried out RT-PCR using two pairs of nested primers. Results showed expression of GFP-mRNA at 24 h post-transfection. Moreover, western blot assays of crude extracts of transfected cysts, carried out using the anti-GFP specific antibody, showed the expected protein band of 27 kDa, demonstrating that the GFP expression started at 24 after plasmid microinjection and was maintained up to 72 h. These findings will facilitate the development of functional genomics approaches applied to this model of cysticercosis.

摘要

人和猪的囊尾蚴病是由扁形虫猪带绦虫(绦虫纲)的幼虫阶段引起的。人脑感染,也称为神经囊尾蚴病,是全球中枢神经系统最常见的寄生虫病。使用粗颈绦虫小鼠模型在疾病理解方面取得了重大进展。我们在此描述粗颈绦虫囊尾蚴的成功转染方案,作为解决目前许多关于囊尾蚴病无法触及的生物学问题的第一步。将质粒pcDNA3.1/NT-GFP-TOPO显微注射到粗颈绦虫囊尾蚴(ORF株)中,该质粒编码由巨细胞病毒启动子(CMV)驱动的绿色荧光蛋白(GFP)。显微注射12小时后,GFP荧光在与囊肿囊壁芽结构相关的区域逐渐形成斑块。荧光在显微注射后24 - 48小时达到峰值,并持续至72小时。使用抗GFP抗体对转染囊肿的组织切片进行免疫组织化学研究,证明抗体与GFP荧光在皮层细胞质和皮层下细胞体中共定位。为了在mRNA水平验证GFP的表达,我们使用两对巢式引物进行了RT-PCR。结果显示转染后24小时GFP-mRNA表达。此外,使用抗GFP特异性抗体对转染囊肿的粗提物进行蛋白质印迹分析,显示出预期的27 kDa蛋白条带,表明GFP表达在质粒显微注射后24小时开始,并持续至72小时。这些发现将有助于开发应用于这种囊尾蚴病模型的功能基因组学方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ba8/4571025/610053053e10/40064_2015_1278_Fig1_HTML.jpg

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