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用双抗体夹心信号放大酶联免疫吸附测定法检测感染羊的循环抗原谷胱甘肽S-转移酶

The Detection of Circulating Antigen Glutathione S-Transferase in Sheep Infected with with Double-Antibody Sandwich Signal Amplification Enzyme-Linked Immunosorbent Assay.

作者信息

Duan Jiahui, Zhang Nan, Liu Shaoxiong, Li Jianhua, Gong Pengtao, Wang Xiaocen, Li Xin, Zhang Xu, Tang Bo, Zhang Xichen

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

Animals (Basel). 2024 Feb 3;14(3):506. doi: 10.3390/ani14030506.

Abstract

Fasciolosis is a global zoonotic parasitic disease caused by infection that is particularly harmful to cattle and sheep. A biotin-streptavidin signal amplification ELISA (streptavidin-ELISA/SA-ELISA) based on circulating antigens can allow for the early detection of -infected animals and is suitable for batch detection. It is considered to be a better means of detecting infection than traditional detection methods. In this study, using the serum of sheep artificially infected with , the cDNA expression library of was screened, 17 immunodominant antigen genes of were obtained, and glutathione s-transferase (GST) was selected as the candidate detection antigen. Firstly, the GST cDNA sequence was amplified from , followed by the preparation of recombinant protein GST (rFhGST). Then, monoclonal and polyclonal antibodies against rFhGST were prepared using the GST protein. Afterward, the immunolocalization of the target protein in the worm was observed via confocal microscopy, and it was found that the GST protein was localized in the uterus, intestinal tract, and body surface of . Finally, a double-antibody sandwich SA-ELISA based on the detection of circulating antigens was established. There was no cross-reaction with positive sera infected with (), (), (), or (). Forty serum and fecal samples from the same batch of sheep in Nong'an County, Changchun City, Jilin Province, China were analyzed using the established detection method and fecal detection method. The positive rate of the SA-ELISA was 17.5%, and the positive rate of the fecal detection method was 15%. The detection results of this method were 100% consistent with commercial ELISA kits. A total of 152 sheep serum samples were tested in Nong'an County, Changchun City, Jilin Province, and the positive rate was 5.92%. This study laid the foundation for the development of serological detection preparations for infection based on the detection of circulating antigens.

摘要

肝片吸虫病是一种由感染引起的全球性人畜共患寄生虫病,对牛和羊危害尤为严重。基于循环抗原的生物素 - 链霉亲和素信号放大酶联免疫吸附测定法(链霉亲和素酶联免疫吸附测定法/SA-ELISA)能够实现对感染动物的早期检测,且适用于批量检测。与传统检测方法相比,它被认为是检测感染的更好手段。在本研究中,利用人工感染肝片吸虫的绵羊血清,筛选肝片吸虫的cDNA表达文库,获得了17个肝片吸虫的免疫显性抗原基因,并选择谷胱甘肽S-转移酶(GST)作为候选检测抗原。首先,从肝片吸虫中扩增GST cDNA序列,随后制备重组蛋白GST(rFhGST)。然后,使用GST蛋白制备抗rFhGST的单克隆抗体和多克隆抗体。之后,通过共聚焦显微镜观察目标蛋白在虫体中的免疫定位,发现GST蛋白定位于肝片吸虫的子宫、肠道和体表。最后,建立了基于循环抗原检测的双抗体夹心SA-ELISA。该方法与感染姜片吸虫(Fasciolopsis buski)、日本血吸虫(Schistosoma japonicum)、华支睾吸虫(Clonorchis sinensis)或卫氏并殖吸虫(Paragonimus westermani)的阳性血清均无交叉反应。采用建立的检测方法和粪便检测方法对中国吉林省长春市农安县同一批绵羊的40份血清和粪便样本进行分析。SA-ELISA的阳性率为17.5%,粪便检测方法的阳性率为15%。该方法的检测结果与商业酶联免疫吸附测定试剂盒的结果100%一致。在吉林省长春市农安县共检测了152份绵羊血清样本,阳性率为5.92%。本研究为基于循环抗原检测的肝片吸虫感染血清学检测制剂的开发奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/323b/10854876/cf19f4a4dcc7/animals-14-00506-g001.jpg

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