key: cord-0868622-2aysumyu
authors: Shurrab, Farah M.; Al-Sadeq, Duaa W.; Amanullah, Fathima; Younes, Salma N.; Al-Jighefee, Hadeel; Younes, Nadin; Dargham, Soha R.; Yassine, Hadi M.; Abu Raddad, Laith J.; Nasrallah, Gheyath K.
title: Effect of multiple freeze–thaw cycles on the detection of anti-SARS-CoV-2 IgG antibodies
date: 2021-08-06
journal: J Med Microbiol
DOI: 10.1099/jmm.0.001402
sha: 1d774f273256f106ad58e711f482202393c560d4
doc_id: 868622
cord_uid: 2aysumyu

Several studies have investigated the effect of repeated freeze–thaw (F/T) cycles on RNA detection for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). However, no data are available regarding the effect of repeated F/T cycles on SARS-CoV-2 antibody detection in serum. We investigated the effect of multiple F/T cycles on anti-SARS-CoV-2 IgG detection using an ELISA test targeting the nucleocapsid antibodies. Ten positive and 1 negative SARS-CoV-2 IgG sera from 11 participants, in replicates of 5, were subjected to a total of 16 F/T cycles and stored at 4 °C until tested by ELISA. Statistical analysis was performed to test for F/T cycle effect. None of the 10 positive sera became negative after 16 F/T cycles. There was no significant difference in the OD average reading between the first and last F/T cycles, except for one serum with a minimal decline in the OD. The random effect linear regression of log (OD) on the number of cycles showed no significant trend, with a slope consistent with zero (B=−0.0001; 95 % CI −0.0008; 0.0006; P-value=0.781). These results suggest that multiple F/T cycles had no effect on the ability of the ELISA assay to detect SARS-CoV-2 IgG antibodies.

Serum banks are well established as they are considered to be an essential reference for clinical information and research use. However, there are concerns regarding the effect of repeated freeze-thaw (F/T) cycles on the biological entities of serum proteins, including immunoglobulins (Ig) [1] [2] [3] [4] . It is suspected that repeated F/T cycles may lead to denaturation or degradation of the antibody of interest [5] . This is critical when it comes to sensitive immunoassays such as ELISA or chemiluminescence automated analysers that detect antibodies in serum or plasma. Therefore, it is recommended to store sera in aliquots to reduce sample exposure to multiple F/T cycles [6] . Although several studies have suggested that repeated F/T cycles have a minimal effect on antibody stability against specific pathogens [2, 7, 8] , other researchers are questioning the reliability of the data generated from using such samples [9] .

The emergence of the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in late December 2019 in Wuhan, PR China, has led to a global coronavirus disease 2019 (COVID-19) pandemic [10] . Several studies showed the effect of repeated F/T cycles on SARS-CoV-2 RNA stability in throat and nasopharyngeal swabs specimens [11, 12] . However, to the best of our knowledge, the stability of SARS-CoV-2 antibodies after multiple F/T cycles has not been assessed. In this study, we investigated the effect of multiple F/T cycles on SARS-CoV-2 IgG detection in serum by using ELISA targeting the nucleocapsid (N) antibodies.

The cohort sera used in this study were part of blood specimens that were collected in a previous nationwide survey to assess the prevalence of SARS-CoV-2 detectable antibodies OPEN ACCESS [13] . This study was approved by the Medical Research Centre (MRC) Ethics Committee (MRC-05-136). The specimens were collected between 26 July and 9 September 2020 and frozen and thawed twice during the previous study before being transferred on ice to our facility at Qatar University, where they were stored once more at −80 °C until they were used in this study in December 2020.

Fifty sera were screened using the EDI novel coronavirus COVID-19 IgG ELISA kit (ref. no. KT-1032, USA) targeting the anti-N SARS-CoV2 IgG [14] . Eleven sera were selected from these, of which 10 were IgG-positive and one was IgG-negative. The latter serum was used as a control. For a more representative comparison between measurements, we selected the positive sera that had broadly different optical density (OD) readings (high, medium and low).

From each of the 11 sera, a total of 40 serum aliquots, 5 µl each, were divided into 8 sets of 5 replicates and subjected to 8 different F/T cycles (3, 4, 6, 8, 10, 12, 14 , and 16). The first set was stored at 4 °C during the study as a baseline. The remaining seven sets were subjected to the repeated F/T cycles, with one set of aliquots being stored at 4 °C at a time until all cycles were completed. The serum samples were then tested using the EDI kit and the OD reading at 450 nm was recorded.

The average reading for each serum was estimated and plotted against the number of F/T cycles and versus the cut-off values defining a positive or a negative outcome. The cut-off values were calculated according to the manufacturer's instructions. An independent t-test was conducted to compare the OD measurements of the positive sera and the negative serum. Paired t-test were performed to compare the log (OD) of the first cycle to the log (OD) of the last cycle. To adjust for any clustering effect from measurements of the same serum, a random effect linear regression was conducted on the log (OD) versus the number of F/T cycles. A P-value of <0.05 was considered statistically significant.

A total of 438 measurements from 11 sera were available for analysis. Two OD readings were excluded due to manual error during the ELISA run. The mean OD value for the positive serum measurements [n=398; mean (sd): 0.69 (0.25)] was significantly higher than that of the negative serum measurement [n=40; mean (sd): 0.23 (0.03); P-value<0.001].

The average assay readings for each serum were plotted against the F/T cycles and versus the cut-off values delineated at ≤0.2655 for negatives and ≥0.3245 for positives (Fig. 1) . When antibody OD readings were analysed as categorical outcomes (positive, negative and equivocal) across the cycles, out of 398 positive measurements, 0.8 % (3/398; 95 % CI 0.3-2.2 %) were no longer classified as positive using the positive cut-off. Instead, they were equivocal. Out of 40 negative measurements, 20.0 % (8/40; 95 % CI 10.5-34.8 %) were no longer classified as negative using the negative cut-off (Fig. 2) . Instead, they were equivocal. None of the sera changed from positive to negative or from negative to positive throughout the cycles.

The random effect linear regression of log (OD) on the number of cycles showed no significant trend, with a slope consistent with zero (B=−0.0001; 95 % CI −0.0008; 0.0006; P-value=0.781), indicating that the multiple F/T cycles had no effect on the SARS-CoV-2 IgG antibody titres in the serum.

Frozen serum banks are an important source of scientific and clinical information and are essential for infectious disease and vaccine research. It is commonly believed that antibodies keep their stability if serum is stored below −20C o [9] . Nevertheless, evidence suggests that just one F/T cycle can significantly reduce IgG antibody levels [9] . To date, studies investigating the effects of F/T cycles on the detection of SARS-CoV-2 antibodies have yielded inconsistent results, and the availability of data on the effects of multiple F/T cycles, sample size and storage conditions is limiting.

The present study investigated the effect of 16 repeated F/T cycles on SARS-CoV-2 IgG antibodies in serum. The results showed that in nearly all sera there was no significant difference in sample reactivity between the first and last F/T cycle, while none of the reactive sera became non-reactive after 16 F/T cycles and no false-positive results were obtained (Fig. 2) . The random effect linear regression showed no significant trend in sera OD reading, with a slope that is consistent with zero. However, there was one outlier with one serum showing an increased OD reading after cycle 16 (Fig. 1, sample no. 7) . This outlier may have been caused by a pipetting error between the ELISA plates.

In agreement with our findings, other studies have tested the effect of repeated F/T cycles on measles, mumps, rubella, syphilis, anti-nuclear antibodies (ANA) and antineutrophil cytoplasmic antibodies (ANCA), and found similar results [2, 8, 15] . Although each study applied a different F/T methodology and targeted different antigens, they all concluded that there was no clinically or statistically significant difference in the antibody levels after several F/T cycles. Interestingly, another study has shown that 174 F/T cycles on anti-treponemal sera did not affect the stability, the reactivity of antibodies, or the samples' quality when tested by a chemiluminescence assay [1] . The data generated from our study and the previous studies provide concrete knowledge regarding antibody stability in serum, which allows the maximum potential use of serum, especially for those that have undergone multiple F/T cycles. Additionally, our generated results can be beneficial for the design of serum banks, where it is important to monitor the integrity of sample components.

We conclude that 16 F/T cycles did not interfere with the detection of SARS-CoV-2 IgG antibodies, and had no effect on assay sensitivity. However, in this study, we tested the effect of multiple F/T cycles on anti-SARS-CoV-2 IgG in serum only. It would be ideal to use plasma samples as well and to test the stability of other anti-SARS-CoV-2 antibody classes such as IgM and IgA. Furthermore, our ELISA test targeted antibodies against SARS-CoV-2 nucleocapsid protein alone, but possibly F/T cycles may interfere with other SARS-CoV-2 proteins, such as the spike protein. Lastly, using an automated serological analyser would be beneficial to reduce pipetting errors. 

Effect of multiple freeze-thaw cycles on the stability of positive anti-treponemal serum samples

Effect of multiple freeze and thaw cycles on the sensitivity of IGG and IGM immunoglobulins in the sera of patients with syphilis

Clinical evaluation of the levels of 12 cytokines in serum/plasma under various storage conditions using evidence biochip arrays

The effect of storage time and freeze-thaw cycles on the stability of serum samples

Frozen-state storage stability of a monoclonal antibody: aggregation is impacted by freezing rate and solute distribution

Evaluation of Freeze Thaw Cycles on stored plasma in the Biobank of the Norwegian Mother and Child Cohort study

The impact of repeated freezethaw cycles on antiphospholipid antibody titer

Effect of multiple freeze-thaw cycles on detection of measles, mumps, and rubella virus antibodies

Biologic banking in cohort studies, with special reference to blood

Severe acute respiratory syndrome coronavirus-2 natural animal reservoirs and experimental models: systematic review

Influence of storage conditions on SARS-COV-2 nucleic acid detection in throat swabs

Clinical performance and sample freeze-thaw stability of the cobas®6800 SARS-CoV-2 assay for the detection of SARS-CoV-2 in oro-/nasopharyngeal swabs and lower respiratory specimens

Seroprevalence of SARS-CoV-2 infection in the craft and manual worker population of Qatar

Performance evaluation of five ELISA kits for detecting anti-SARS-COV-2 IgG antibodies

Does multiple freezing and thawing cycles of serum affect the detection of anti-nuclear antibodies and antineutrophil cytoplasmic antibodies by indirect immunofluorescent method?

We would like to thank Dr Nahla Afifi, Director of Qatar Biobank (QBB), Ms Tasneem Al-Hamad, Ms Eiman Al-Khayat and the rest of the QBB team for their unwavering support in retrieving and analysing samples and in compiling and generating databases for COVID-19 infection, as well as Dr Asma Al-Thani, Chairperson of the Qatar Genome Programme Committee and Board Vice Chairperson of QBB, for her leadership of this effort. 

The authors declare that there are no conflicts of interest.

This study was approved by the Medical Research Centre (MRC) Ethics Committee, approval number MRC-05-136.

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