Chang Yu-Chih, Shimoda Hiroshi, Wen Hsiao-Wei, Maeda Ken, Tseng Ching-Yu, Tsai Ching-Hsiu, Hsu Wei-Li
Doctoral Program in Microbial Genomics, National Chung Hsing University and Academia Sinica, 145 Xingda Rd., South Dist., Taichung City, 402, Taiwan.
Graduate Institute of Microbiology and Public Health, College of Veterinary Medicine, National Chung Hsing University, Taichung, Taiwan.
Virol J. 2025 Jun 30;22(1):210. doi: 10.1186/s12985-025-02840-5.
Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV) is a zoonotic pathogen that affects various animal species, often asymptomatically, while causing fatal disease in humans. Current serological tests are limited, which led to the development of novel diagnostic assays targeting the viral nucleoprotein (NP), a conserved and immunodominant protein across SFTSV strains. This study validated the new diagnostics using field monkey sera, employing Enzyme-Linked Immunosorbent Assay (ELISA) with infected cell lysate (ICL-ELISA) as the antigen. Immunoblotting with recombinant NP (rNP) demonstrated 94.6% specificity and 96.3% sensitivity for anti-NP antibody detection. As NP exists in both monomeric and RNA-binding oligomeric forms, rNP was expressed in both configurations and used for ELISA and rapid lateral flow assays (LFA). The oligomeric rNP exhibited superior antigenicity, achieving 97.3% specificity and 92.6% sensitivity, outperforming ICL-ELISA. Additionally, oligomer-enriched rNP was applied to develop an LFA test strip, where rNP conjugated with magnetic nanoparticles enhanced immunocomplex enrichment and clarity. The NP Ab-LFA test achieved 84.2% specificity and 100% sensitivity, successfully detecting anti-NP antibodies in rabbit, mouse, and monkey sera. These innovative diagnostic tools offer reliable methods for detecting SFTSV antibodies, facilitating disease control and mitigating the risk of human outbreaks.
严重发热伴血小板减少综合征病毒(SFTSV)是一种人畜共患病原体,可感染多种动物物种,通常无症状,但会导致人类致命疾病。目前的血清学检测方法有限,这促使人们开发针对病毒核蛋白(NP)的新型诊断检测方法,NP是一种在SFTSV毒株中保守且具有免疫优势的蛋白。本研究使用野外猴子血清验证了这种新的诊断方法,采用以感染细胞裂解物(ICL-ELISA)为抗原的酶联免疫吸附测定(ELISA)。用重组NP(rNP)进行免疫印迹显示,检测抗NP抗体的特异性为94.6%,灵敏度为96.3%。由于NP以单体和RNA结合寡聚体两种形式存在,rNP以两种构型表达,并用于ELISA和快速侧向流动分析(LFA)。寡聚体rNP表现出优异的抗原性,特异性达到97.3%,灵敏度达到92.6%,优于ICL-ELISA。此外,富含寡聚体的rNP被用于开发LFA试纸条,其中与磁性纳米颗粒偶联的rNP增强了免疫复合物的富集和清晰度。NP Ab-LFA检测的特异性为84.2%,灵敏度为100%,成功检测出兔、小鼠和猴子血清中的抗NP抗体。这些创新的诊断工具为检测SFTSV抗体提供了可靠的方法,有助于疾病控制并降低人类爆发疫情的风险。