Development of a quantum dots based immunochromatographic strip for rapid and on-site detection of African swine fever virus

非洲猪瘟病毒 检出限 量子点 病毒学 硝化棉 病毒 多克隆抗体 单克隆抗体 抗体 抗原 分子生物学 生物 化学 色谱法 纳米技术 材料科学 免疫学 生物化学
作者
Yuxiang Wu,C Wang,Jinzhi Yu,Frolova Ma,Jie Liu,Jing Tan,Guanggang Qu
出处
期刊:Microbial Pathogenesis [Elsevier]
卷期号:: 106669-106669
标识
DOI:10.1016/j.micpath.2024.106669
摘要

African swine fever (ASF) is a lethal disease caused by ASF virus (ASFV), severely impacting the global swine industry. Though nuclear acid-based detection methods are reliable, they are laboratory-dependent. In this study, we developed a device-independent, user friendly and cost-effective quantum dots based immunochromatographic strip (QDs-ICS) with high specificity and sensitivity for the rapid and on-site detection of ASFV antigen. For the preparation of the QDs-ICS, we generated a monoclonal antibody (mAb) mAb-8G8 and polyclonal antibody (pAb) against ASFV-p72 protein. The pAb was labelled with QDs to be used as the detection probe and the mAb-8G8 was coated on the nitrocellulose membrane as the test line. Our results proved that the strip displayed no cross-reactivity with other swine viruses and detection limit of the QDs-ICS was down to 1 ng/mL for the ASFV-p72 protein with great reproducibility. The strip also exhibited high stability with a storage period up to 12 months under room temperature. Twenty blind samples and one hundred clinical samples were examined by the QDs-ICS, conventional PCR and real-time PCR method, respectively. Results showed that the agreement rate between the QDs-ICS and PCR method was 100%, and the agreement rate between the strip and real-time PCR was 94%. The novel QDs-ICS developed here would be an effective tool for on-site detection of ASFV.
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