Inagaki Eri, Sakai Mizuki, Hirano Minato, Muto Memi, Kobayashi Shintaro, Kariwa Hiroaki, Yoshii Kentaro
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.
Ticks Tick Borne Dis. 2016 Jul;7(5):723-729. doi: 10.1016/j.ttbdis.2016.03.002. Epub 2016 Mar 4.
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.
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。