key: cord-0800928-0s2hsnjv
authors: Sekirov, Inna; Petric, Martin; Carruthers, Erin; Lawrence, David; Pidduck, Tamara; Kustra, Jesse; Laley, Jonathan; Lee, Min-Kuang; Chahil, Navdeep; Mak, Annie; Levett, Paul N.; Mendoza, Emelissa; Wood, Heidi; Drebot, Mike; Krajden, Mel; Morshed, Muhammad
title: Performance comparison of micro-neutralization assays based on surrogate SARS-CoV-2 and WT SARS-CoV-2 in assessing virus-neutralizing capacity of anti-SARS-CoV-2 antibodies
date: 2021-08-26
journal: Access Microbiol
DOI: 10.1099/acmi.0.000257
sha: 8bfb50cd1c3e8ea7ce493fa42d352decb0b1b27e
doc_id: 800928
cord_uid: 0s2hsnjv

We compared neutralization assays using either the wild-type severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus or surrogate neutralization markers, using characterized sera. We found the results of the neutralization assays 75 % concordant overall and 80 % concordant for samples with high antibody levels. This demonstrates that commercial surrogate SARS-CoV-2 assays offer the potential to assess anti-SARS-CoV-2 antibodies’ neutralizing capacity outside CL-3 laboratory containment.

Nucleic acid testing is the standard for diagnosing acute severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection [1] . However, serological tests are instrumental in determining other epidemic factors such as community prevalence and asymptomatic infection rates [2] . Many commercially available highly sensitive and specific SARS-CoV-2 serological tests have been developed. Most of these detect antibodies that bind different structural epitopes, but cannot indicate the antibody's virus-neutralizing capacity, namely the inhibition of virus replication by the patient serum. The gold standard for this is the plaque reduction neutralization test (PRNT), a lengthy multi-step test performed using live virus [3] . During the severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1) outbreak, an alternative micro-neutralization antibody assay was implemented [4] , measuring antibody-mediated inhibition of viral cytopathic effect in tissue culture. The micro-neutralization method has also been successfully used to test the neutralizing capacity of anti-H1N1 serum [5] . The micro-neutralization assay can also be applied to determine the SARS-CoV-2-neutralizing antibody levels of convalescent sera. However, SARS-CoV-2 is an RG3 pathogen, and so tests such as PRNT and micro-neutralization can only be performed in appropriate containment (CL-3) laboratory facilities. An alternative approach to the use of live SARS-CoV-2 is to produce pseudoviruses in VSV or lentivirus systems that carry the spike protein of SARS-CoV-2. Pseudovirus neutralization can be shown via the micro-neutralization method and can be performed under CL-2 containment, but still requires cell culture. In this report we describe the results of testing using a cell cultureindependent commercial ELISA assay, designated as the surrogate virus neutralization test (sVNT), which measures the seruminduced inhibition of SARS-CoV-2 spike protein receptor binding domain (RBD) attachment to the host cell receptor, angiotensin converting enzyme-2 (ACE-2).

Two panels of serum samples were studied. A serum panel from the National Microbiology Laboratory (NML) included sera from 21 PCR-confirmed SARS-CoV-2 patients and 19 sera from patients who were not infected with SARS-CoV-2. A BCCDC PHL serum panel comprised 42 sera from PCR-confirmed and sero-positive COVID-19 patients, and 49 sera collected OPEN ACCESS before the onset of the coronavirus disease 2019 (COVID-19) pandemic. All sera from COVID-19 PCR-confirmed patients had been shown to be reactive for anti-SARS-CoV-2 antibodies by at least two commercial assays that detected anti-spike antibodies: Siemens ADVIA Centaur SARS-CoV-2 Total (S1 RBD antigen) and Ortho Vitros SARS-CoV-2 total antibody (RBD antigen). Further, 39/42 samples were also reactive by a third commercial assay that detected anti-nucleocapsid antibodies (Abbott SARS-CoV-2 IgG assay). Samples that were reactive on commercial platforms were selected to represent a range of signal to cut-off (S/CO) ratios.

The challenge virus used in these assays was obtained from the NML, and was designated as hCoV-19/Canada/ON-VIDO-01-2020. The cVNT was carried out as follows: twofold dilutions of sera were heated at 56 °C for 30 min to inactivate complement. To each dilution, 100 TCID 50 of SARS-CoV-2 was added, incubated for 2 h at 37 °C, and then transferred to microtitre plate wells containing monolayers of Vero E6 cells. Each sample was tested in duplicate. The development of cytopathic effect (CPE) was monitored over 3 days; the neutralizing titre was the lowest dilution without CPE. If only one well at the 1 : 8 dilution showed CPE, the CVNT result was recorded as equivocal.

The SARS-CoV-2 PRNT was performed as described elsewhere [6] .

The highest serum dilutions resulting in 50 and 90% reduction in plaques compared with controls were defined as the PRNT 50 and PRNT 90 endpoint titres, respectively. PRNT 50 titres and PRNT 90 titres ≥1 : 20 were considered positive for SARS-CoV-2neutralizing antibodies.

sVNT tests (GenScript USA, Inc., NJ, USA) were performed following the manufacturer's instructions. Diluted sera (1 : 9 dilution) were mixed with HRP-conjugated SARS-CoV-2 RBD at 1 : 1 ratio and incubated at 37 °C for 30 min. One hundred microlitres of the mixture was added to a microtitre plate and incubated at 37 °C for 15 min. The plate was then washed four times with wash buffer, before the addition of 100 µl 3,3′,5,5′-tetra-methylbenzidine solution per well, followed by incubation in the dark at 20-25 °C for 15 min. Stop solution was added to each well and the plate was read immediately at 450 nm. Results were considered to be positive for neutralizing antibodies if the percentage inhibition of the sample was 20 % or greater.

For the NML panel, PRNT 50 /PRNT 90 , cVNT and sVNT assays yielded comparable results for all 40 samples (Table 1) . Of 19 SARS-CoV-2-negative samples, 1 sample had detectable neutralizing capacity by sVNT but not PRNT 50 /PRNT 90 and cVNT assays. This sample was obtained from a recovered SARS-CoV-1 patient and the cross-reaction is not entirely surprising, considering the ~73 % similarity of the RBD motif of the two viruses. The only other SARS-CoV-1-positive sample on the panel was negative by all three tested assays. Of 21 samples from SARS-CoV-2-positive patients, 20 had fully concordant positive results by all assays and 1 had a positive sVNT and PRNT 50 result but negative cVNT and PRNT 90 results, potentially indicative of the ability of sVNT assay to detect low(er) levels of neutralizing antibodies (Table 1) .

All BCCDC PHL samples negative for SARS-CoV-2 antibodies by high-volume platforms (Siemens, Ortho and Abbott) were also negative on the sVNT assay and had titres of <1 : 8 on cVNT ( Table 2 ). All negative samples showed inhibition of binding of less than 11 % in the sVNT. All samples that tested positive by commercial serology assays (n=42) were positive for inhibition by sVNT, but cVNT results were variable (Table 2) . For samples testing positive in both cVNT and sVNT assays, the extent of antibody-mediated inhibition of binding to ACE-2 did not correlate with time of sample collection from disease onset, with variable levels of inhibition observed at both periods. The level of inhibition in sVNT showed a higher correlation with indices generated in the Siemens assay (Fig. 1a) than with the S/CO ratios of either the Abbott and Ortho assays (Fig. 1b, c) . Samples from known positive patients with negative cVNT titres (<1 : 8) showed lower inhibition by sVNT compared to samples positive for neutralizing antibodies by both assays (44 vs 92 %). For the BCCDC panel, there was an overall positive agreement of 62 % between the sVNT and cVNT assays for COVID-19-positive sera and 100 % negative agreement on pre-pandemic sera; positive agreement increased to 71 % when equivocal results by cVNT were counted as positive.

We compared the GenScript sVNT assay to cVNT, PRNT and commercial CLIA assays. There was a high concordance of results for PRNT, cVNT and sVNT assays on the panel received from the sVNT-cVNT concordance was greater for samples with higher S/ CO ratios in commercial assays, but test outcome was unaffected by time of collection from disease onset. Similar findings were reported recently using two sVNT assays [7] . This is in contrast to recently reported results for GenScript sVNT, wherein samples collected >14 days post-disease onset were more likely to be positive by sVNT than samples collected <14 days after onset [8] . Moreover, while Meyer et al. [8] found a pseudovirus-based VNT assay to be more sensitive than the GenScript sVNT assay, we found that the GenScript sVNT assay, at least in our hands, was more sensitive than a SARS-CoV-2-based cVNT assay. This could be due to the different in vitro infectivity of SARS-CoV-2 vs the VSV-based pseudovirus for host cells, as well as the variability of epitopes present for neutralization on SARS-CoV-2 virus, vs those utilized in the production of pseudovirus constructs, vs those utilized in the production of competitive inhibition surrogate neutralization assays. Given that during the natural infection, the host immune system is expected to generate antibodies against an array of exposed epitopes, partial availability of epitopes for neutralization/inhibition may contribute to differences in results between cVNT, sVNT and pseudovirus VNT assays. This, similarly, can also play into the discrepancies with regard to the presence/absence of observed differences in neutralizing capacity of sera collected early/later post-infection. Depending on whether the epitope of choice for the surrogate or pseudovirus system is the main target of generated antibodies both early and later in infection, the expected results would differ. Such considerations might become particularly important when assessing cross-neutralizing capacity post-vaccination vs post-infection with different variant strains of SARS-CoV-2.

If sVNT is indeed able to detect lower titres of neutralizing antibodies, it is yet to be determined whether these lower levels translate into in vivo virus-neutralizing capacity. Similarly, the potential requirement to modify 'positive' cut-offs on sVNT assay(s) for observed inhibitory effect needs to be evaluated. Interpretations of all these assays are further complicated by the fact that there are currently no clear in vivo correlates established for either the cVNT or the PRNT 50/90 assays.

A limited number of studies have been conducted on SARS CoV-2 neutralization tests [9, 10] . It has been shown that neutralizing antibody titres may vary among recovered COVID-19 patients [11] , which suggests that other immune markers such as T -cells and cytokines are likely to contribute to viral clearance. Recently, Prévost et al. [12] found the neutralizing capacity of serum to substantially decrease in hospitalized COVID-19 patients over time, which is somewhat concordant with our cVNT findings.

Whether and over what period neutralizing antibody titres correlate with protection in vivo still needs to be determined. Laboratory-developed [13] and commercially available sVNT assays allow for accessible high-volume assessments of antibody neutralizing capacity [14] . However, where clinical applications are concerned, suitable positive and negative cut-offs, ideally against in vivo correlates of protection, need to be evaluated and established.

This work was funded by Genome BC on project COV-050.

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The authors are grateful to the National Microbiology Laboratory for providing us with the blinded serum panel and to BCCDC PHL and NML laboratory staff for carrying out all testing. We would also like to thank Phoenix Airmid Biomedical, ON, Canada for providing commercial kits (GenScript USA, Inc., NJ, USA). We thank Karen Chu for critically reading and editing the manuscript.

These authors contributed equally to this work.

The authors declare that there are no conflicts of interest.

The study was authorized by the Provincial Health Officer and approved by the Clinical Research Ethics Board of the University of British Columbia (H20-01089).