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Diagnostics of severe acute respiratory syndrome-associated coronavirus (SARS-CoV) nucleocapsid antigen using chicken immunoglobulin Y.

机译:使用鸡免疫球蛋白Y诊断严重急性呼吸系统综合症相关冠状病毒(SARS-CoV)核衣壳抗原。

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The goal of this study was to develop a quantitative detection system for severe acute respiratory syndrome-associated coronavirus (SARS-CoV), targeting the nucleocapsid protein (NP), to determine the presence and degree of infection in suspected individuals. Because the NP is the viral protein shed during infection and its template mRNA is the most abundant subgenomic RNA, it is a suitable candidate for developing antibodies for diagnostic applications. In this study, we have prepared full-length SARS-CoV NP expressed in Escherichia coli and purified. Full-length NP was used for the preparation of mouse monoclonal antibody and chicken polyclonal IgY antibodies for the development of heterosandwich ELISA for early diagnostics of SARS-suspected individuals. The sensitivity of the developed heterosandwich ELISA can detect the viral antigen at 18.5 pg/mL of recombinant NP. This study describes ultrasensitive ELISA using 19B6 monoclonal antibody as the capture antibody and IgY as the detecting antibody against the most abundant SARS-CoV NP antigens. One of the most important findings was the use of inexpensive polyclonal IgY antibody to increase the sensitivity of the detection system for SARS-CoV at the picogram level. Furthermore, the immunoassay of SARS-CoV NP antigen developed could be an effective and sensitive method of diagnosing SARS-suspected individuals during a future SARS-CoV outbreak.
机译:这项研究的目标是开发针对核衣壳蛋白(NP)的严重急性呼吸综合征相关冠状病毒(SARS-CoV)定量检测系统,以确定可疑个体的存在和感染程度。由于NP是感染过程中脱落的病毒蛋白,其模板mRNA是最丰富的亚基因组RNA,因此它是开发用于诊断应用的抗体的合适候选者。在这项研究中,我们制备了在大肠杆菌中表达并纯化的全长SARS-CoV NP。全长NP用于制备小鼠单克隆抗体和鸡多克隆IgY抗体,用于开发异夹心ELISA,以早期诊断SARS疑似个体。所开发的异源夹心ELISA的灵敏度可以检测18.5 pg / mL重组NP的病毒抗原。这项研究描述了超敏感的ELISA,使用19B6单克隆抗体作为捕获抗体,而IgY作为针对最丰富的SARS-CoV NP抗原的检测抗体。最重要的发现之一是使用廉价的多克隆IgY抗体来提高皮克级SARS-CoV检测系统的灵敏度。此外,开发的SARS-CoV NP抗原免疫测定方法可能是诊断未来SARS-CoV爆发期间可疑的SARS个体的有效且灵敏的方法。

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