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利用亚病毒颗粒开发一种针对蜱传脑炎病毒的血清诊断多物种酶联免疫吸附测定法。

Development of a serodiagnostic multi-species ELISA against tick-borne encephalitis virus using subviral particles.

作者信息

Inagaki Eri, Sakai Mizuki, Hirano Minato, Muto Memi, Kobayashi Shintaro, Kariwa Hiroaki, Yoshii Kentaro

机构信息

Laboratory of Public Health, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido 060-0818, Japan.

Laboratory of Public Health, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido 060-0818, Japan.

出版信息

Ticks Tick Borne Dis. 2016 Jul;7(5):723-729. doi: 10.1016/j.ttbdis.2016.03.002. Epub 2016 Mar 4.

Abstract

Tick-borne encephalitis virus (TBEV) is a zoonotic agent causing severe encephalitis in humans. A wide range of animal species could be infected with TBEV in endemic areas. A serological survey of wild animals is effective in identifying TBEV-endemic areas. Safe, simple, and reliable TBEV serodiagnostic tools are needed to test animals. In this study, ELISA was developed to detect anti-TBEV specific antibodies in multi-species of animals, using recombinant subviral particles (SPs) with an affinity tag and protein A/G. A Strep-tag was fused at the N terminus of the E protein of the plasmid coding TBEV prME. The E proteins with Strep-tag were secreted as SPs, of which Strep-tag was exposed on the surface. The tagged E proteins were associated with prM. The SPs with Strep-tag were applied as the antigen of ELISA, and TBEV-specific antibodies were detected by the protein A/G. Compared to neutralization test results, the ELISA showed 96.8% sensitivity and 97.7% specificity in rodents and 95.1% sensitivity and 96.0% specificity in humans, without cross-reactivity with antibodies to Japanese encephalitis virus. These results indicate that our ELISA would be useful to detect TBE-specific antibodies in a wide range of animal species.

摘要

蜱传脑炎病毒(TBEV)是一种人畜共患病原体,可导致人类严重脑炎。在流行地区,多种动物物种都可能感染TBEV。对野生动物进行血清学调查有助于确定TBEV流行地区。需要安全、简单且可靠的TBEV血清诊断工具来检测动物。在本研究中,利用带有亲和标签和蛋白A/G的重组亚病毒颗粒(SPs)开发了ELISA,用于检测多种动物体内的抗TBEV特异性抗体。在编码TBEV prME的质粒的E蛋白N端融合了一个链霉亲和素标签。带有链霉亲和素标签的E蛋白以SPs形式分泌,其中链霉亲和素标签暴露在表面。带标签的E蛋白与prM相关联。将带有链霉亲和素标签的SPs用作ELISA的抗原,通过蛋白A/G检测TBEV特异性抗体。与中和试验结果相比,该ELISA在啮齿动物中的灵敏度为96.8%,特异性为97.7%;在人类中的灵敏度为95.1%,特异性为96.0%,且与日本脑炎病毒抗体无交叉反应。这些结果表明,我们开发的ELISA可用于检测多种动物物种中的TBE特异性抗体。

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