Williams Laura, Jurado Silvia, Llorente Francisco, Romualdo Alberto, González Sara, Saconne Ana, Bronchalo Isabel, Martínez-Cortes Mercedes, Pérez-Gómez Beatriz, Ponz Fernando, Jiménez-Clavero Miguel Ángel, Lunello Pablo
Agrenvec S.L., Madrid, Spain.
Centro de Investigación en Sanidad Animal (CISA), Centro Nacional Instituto de Investigación y Tecnología Agraria y Alimentaria (INIA-CSIC), Valdeolmos, Spain.
Front Plant Sci. 2021 Jul 27;12:699665. doi: 10.3389/fpls.2021.699665. eCollection 2021.
The fight against the current coronavirus disease 2019 (COVID-19) pandemic has created a huge demand of biotechnological, pharmaceutical, research and sanitary materials at unprecedented scales. One of the most urgent demands affects the diagnostic tests. The growing need for rapid and accurate laboratory diagnostic tests requires the development of biotechnological processes aimed at producing reagents able to cope with this demand in a scalable, cost-effective manner, with rapid turnaround times. This is particularly applicable to the antigens employed in serological tests. Recombinant protein expression using plants as biofactories is particularly suitable for mass production of protein antigens useful in serological diagnosis, with a neat advantage in economic terms.
We expressed a large portion of the nucleoprotein (N) derived from SARS-CoV-2 in plants. After purification, the recombinant N protein obtained was used to develop an indirect enzyme-linked immunosorbent assay (ELISA) for detection of antibodies to SARS-CoV-2 in human sera. To validate the ELISA, a panel of 416 sera from exposed personnel at essential services in Madrid City Council were tested, and the results compared to those obtained by another ELISA, already validated, used as reference. Furthermore, a subset of samples for which RT-PCR results were available were used to confirm sensitivity and specificity of the test.
The performance of the N protein expressed in plants as antigen in serologic test for SARS-CoV-2 antibody detection was shown to be highly satisfactory, with calculated diagnostic sensitivity of 96.41% (95% CI: 93.05-98.44) and diagnostic specificity of 96.37 (95% CI: 93.05-98.44) as compared to the reference ELISA, with a kappa (K) value of 0.928 (95% CI:0.892-0.964). Furthermore, the ELISA developed with plant-derived N antigen detected SARS-CoV-2 antibodies in 84 out of 93 sera from individuals showing RT-PCR positive results (86/93 for the reference ELISA).
This study demonstrates that the N protein part derived from SARS-CoV-2 expressed in plants performs as a perfectly valid antigen for use in COVID-19 diagnosis. Furthermore, our results support the use of this plant platform for expression of recombinant proteins as reagents for COVID-19 diagnosis. This platform stands out as a convenient and advantageous production system, fit-for-purpose to cope with the current demand of this type of biologicals in a cost-effective manner, making diagnostic kits more affordable.
抗击当前的2019冠状病毒病(COVID-19)大流行产生了对生物技术、制药、研究和卫生材料前所未有的巨大需求。其中最紧迫的需求之一影响到诊断检测。对快速、准确的实验室诊断检测的需求不断增加,这就需要开发生物技术工艺,以可扩展、具有成本效益且周转时间短的方式生产能够满足这一需求的试剂。这尤其适用于血清学检测中使用的抗原。利用植物作为生物工厂进行重组蛋白表达特别适合大规模生产用于血清学诊断的蛋白抗原,在经济方面具有明显优势。
我们在植物中表达了来自严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的大部分核蛋白(N)。纯化后,将获得的重组N蛋白用于开发一种间接酶联免疫吸附测定(ELISA),以检测人血清中针对SARS-CoV-2的抗体。为了验证该ELISA,对来自马德里市议会重要服务部门接触人员的416份血清样本进行了检测,并将结果与另一种已验证的用作参考的ELISA所获得的结果进行比较。此外,使用一部分可获得逆转录聚合酶链反应(RT-PCR)结果的样本,以确认该检测的敏感性和特异性。
在用于SARS-CoV-2抗体检测的血清学检测中,植物中表达的N蛋白作为抗原的性能表现非常令人满意,与参考ELISA相比,计算得出的诊断敏感性为96.41%(95%置信区间:93.05-98.44),诊断特异性为96.37(95%置信区间:93.05-98.44),kappa(K)值为0.928(95%置信区间:0.892-0.964)。此外,用植物源N抗原开发的ELISA在93份RT-PCR结果呈阳性的个体血清中的84份中检测到了SARS-CoV-2抗体(参考ELISA为86/93)。
本研究表明,植物中表达的来自SARS-CoV-2的N蛋白部分作为抗原可完美有效地用于COVID-19诊断。此外,我们的结果支持使用这个植物平台来表达重组蛋白,作为COVID-19诊断的试剂。这个平台是一个方便且有利的生产系统,适合以具有成本效益的方式满足当前对这类生物制品的需求,使诊断试剂盒更具可承受性。