The effect of heat inactivation of ferrets serum samples on the detection of SARS-CoV-2-specific IgG antibodies in elisa

A. Goshina, V. Matyushenko, S. Donina, I. Sychev, I. Isakova-Sivak, A. Katelnikova, L. Rudenko
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Abstract

BACKGROUND: Determination of serum antibody levels to the novel coronavirus SARS-CoV-2 is a necessary tool for assessing humoral immunity in COVID-19 patients or individuals vaccinated with specific vaccines, as well as for studying the immune responses to the viral antigens in animal models. Serum specimens of infected humans and animals are considered potentially infectious material, and therefore heat inactivation of samples at 56 C for 1 hour is recommended to reduce the risk of infection of personnel during serological studies. However, this procedure may affect the detection of virus-specific IgG and IgM antibodies, making interpretation of the results difficult. AIM: The goal is to evaluate the effect of heat inactivation of ferret serum samples on the binding of IgG antibodies to the SARS-CoV-2 antigens. MATERIALS AND METHODS: Serum samples of SARS-CoV-2 naive and immune ferrets were analyzed in three variants: (1) native sera, (2) serum samples than were heated at 56C for 1 hour, and (3) serum samples that were treated with receptor-degrading enzyme (RDE). The samples were studied in enzyme-linked immunosorbent assay (ELISA) using recombinant RBD protein (receptor-binding domain of SARS-CoV-2 S-protein) as a substrate, followed by determination of specific antibody levels before and after treatments. RESULTS: It has been shown that heat inactivation of the ferrets naive serum samples can lead to false-positive results, while RDE treatment can neutralize the effect of non-specific binding of IgG antibodies to the RBD domain of the SARS-CoV-2 S protein. CONCLUSIONS: Structural rearrangement of SARS-CoV-2-specific IgG antibodies and the formation of immunoglobulin complexes during heat inactivation of serum samples can affect the avidity of the antigen-antibody complex and lead to false-positive results when performing enzyme immunoassay. One of the possible methods to reduce the risk of artifacts is the treatment of blood sera with RDE, which eliminates the effect of heat inactivation.
热灭活雪貂血清对elisa法检测sars - cov -2特异性IgG抗体的影响
背景:检测新型冠状病毒SARS-CoV-2的血清抗体水平是评估COVID-19患者或接种特异性疫苗个体体液免疫的必要工具,也是研究动物模型对病毒抗原免疫反应的必要工具。受感染的人和动物的血清标本被认为是潜在的传染性物质,因此建议在56℃下对样品进行1小时的热灭活,以减少血清学研究期间人员感染的风险。然而,这种方法可能会影响病毒特异性IgG和IgM抗体的检测,使结果难以解释。目的:评价热灭活雪貂血清样品对SARS-CoV-2抗原IgG抗体结合的影响。材料与方法:对SARS-CoV-2原生和免疫雪貂血清样本进行三种变异分析:(1)天然血清,(2)56℃加热1小时的血清样本,(3)受体降解酶(RDE)处理的血清样本。以重组RBD蛋白(SARS-CoV-2 s蛋白受体结合域)为底物,采用酶联免疫吸附试验(ELISA)对样品进行研究,然后测定治疗前后的特异性抗体水平。结果:研究表明,对雪貂血清样品进行热灭活可导致假阳性结果,而RDE处理可中和非特异性结合IgG抗体对sars - cov - 2s蛋白RBD结构域的影响。结论:血清样品热失活过程中sars - cov -2特异性IgG抗体的结构重排和免疫球蛋白复合物的形成会影响抗原-抗体复合物的活性,导致酶免疫测定结果出现假阳性。降低伪影风险的可能方法之一是用RDE处理血清,它消除了热失活的影响。
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