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β-贾第虫蛋白作为囊肿多宿主检测的免疫磁珠富集靶点

β-Giardin as an Immunomagnetic Enrichment Target for Multi-Host Detection of Cysts.

作者信息

Wang Hongyu, Yang Heng, Li Chaofan, Chen Mengge, Wang Xiaocen, Zhang Xu, Gong Pengtao, Zhang Nan, Zhang Xichen, Li Jianhua, Li Xin

机构信息

State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, China.

出版信息

Pathogens. 2025 Sep 11;14(9):918. doi: 10.3390/pathogens14090918.

Abstract

Giardiasis is a globally prevalent waterborne zoonosis. Rapid enrichment and detection technologies for this disease are essential. Cyst outer wall proteins are ideal targets for the enrichment and detection of cysts in the environment, but there are few available targets with suboptimal effectiveness. In this study, () cysts were purified, and outer wall proteins were biotinylated, followed by streptavidin magnetic bead purification and mass spectrometry. Sixty-three novel cyst wall proteins were identified, and their functions were annotated through Gene Ontology (GO) and KEGG analyses. The β-giardin and α-1 giardin were among the newly identified and predicted to be located on the outer wall of cysts. For the characterization of these two targets, we applied sequence analysis, prokaryotic expression, preparation of polyclonal antibodies, and determination of subcellular localization. Finally, based on β-giardin immunomagnetic beads were prepared using the polyclonal antibodies and tested for their enrichment efficiency. Immunomagnetic beads targeting β-giardin achieved 65% cyst enrichment efficiency in fecal samples, comparable to conventional methods. Clinical evaluation across 163 multi-host fecal samples (ferrets, Siberian tigers, red-crowned cranes) demonstrated concordance with nested PCR, successfully enriching cysts from PCR-positive specimens. The immunomagnetic beads method targeting β-giardin demonstrated effective cyst enrichment in multi-host fecal samples. These results provide a proteomic framework for the cyst wall proteins of , expanding the detection targets for cysts. It also establishes a theoretical foundation for subsequent research on the composition and function of cysts.

摘要

贾第虫病是一种全球流行的水源性人畜共患病。针对该疾病的快速富集和检测技术至关重要。包囊外壁蛋白是环境中包囊富集和检测的理想靶点,但可用靶点较少且效果欠佳。在本研究中,纯化了()个包囊,并对其外壁蛋白进行生物素化,随后通过链霉亲和素磁珠纯化和质谱分析。鉴定出63种新的包囊壁蛋白,并通过基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析对其功能进行注释。β-贾第素和α-1贾第素是新鉴定出的,预计位于包囊外壁。为了表征这两个靶点,我们进行了序列分析、原核表达、多克隆抗体制备以及亚细胞定位测定。最后,基于β-贾第素,使用多克隆抗体制备免疫磁珠并测试其富集效率。靶向β-贾第素的免疫磁珠在粪便样本中实现了65%的包囊富集效率,与传统方法相当。对163份多宿主粪便样本(雪貂、东北虎、丹顶鹤)进行的临床评估表明,与巢式PCR结果一致,成功从PCR阳性标本中富集了包囊。靶向β-贾第素的免疫磁珠法在多宿主粪便样本中显示出有效的包囊富集效果。这些结果为贾第虫的包囊壁蛋白提供了一个蛋白质组学框架,扩大了贾第虫包囊的检测靶点。这也为后续关于贾第虫包囊组成和功能的研究奠定了理论基础。

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