Publication: Automated Western immunoblotting detection of anti-SARS-CoV-2 serum antibodies
| dc.contributor.author | Edouard, S. | |
| dc.contributor.author | Jaafar, R. | |
| dc.contributor.author | Orain, N. | |
| dc.contributor.author | Parola, P. | |
| dc.contributor.author | Colson, P. | |
| dc.contributor.author | La Scola, B. | |
| dc.contributor.author | Fournier, P. -E. | |
| dc.contributor.author | Raoult, D. | |
| dc.contributor.author | Drancourt, M. | |
| dc.date.accessioned | 2024-11-30T03:49:23Z | |
| dc.date.available | 2024-11-30T03:49:23Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | ELISA and chemiluminescence serological assays for COVID-19 are currently incorporating only one or two SARS-CoV-2 antigens. We developed an automated Western immunoblotting as a complementary serologic assay for COVID-19. The JessTM Simple Western system, an automated capillary-based assay, was used, incorporating an inactivated SARS-CoV-2 lineage 20a strain as the source of antigen, and total immunoglobulins (IgG, IgM, IgA) detection. In total, 602 sera were tested including 223 from RT-PCR-confirmed COVID-19 patients, 76 from patients diagnosed with seasonal HCoVs and 303 from coronavirus-negative control sera. We also compared this assay with the EUROIMMUN® SARS-CoV-2 IgG ELISA kit. Among 223 sera obtained from RT-PCR-confirmed COVID-19 patients, 180/223 (81%) exhibited reactivity against the nucleocapsid and 70/223 (31%) against the spike protein. Nucleocapsid reactivity was further detected in 9/76 (14%) samples collected from patients diagnosed with seasonal HCoVs and in 15/303 (5%) coronavirus-negative control samples. In the subset of sera collected more than 2 weeks after the onset of symptoms, the sensitivity was 94% and the specificity 93%, the latter value probably reflecting cross-reactivity of SARS-CoV-2 with other coronaviruses. The automated Western immunoblotting presented a substantial agreement (90%) with the compared ELISA (Cohen’s Kappa=0.64). Automated Western immunoblotting may be used as a second line test to monitor exposure of people to HCoVs including SARS-CoV-2. © 2021, The Author(s). | |
| dc.format.extent | С. 1309-1317 | |
| dc.identifier.citation | Automated Western immunoblotting detection of anti-SARS-CoV-2 serum antibodies / Edouard, S. [et al.] // European Journal of Clinical Microbiology and Infectious Diseases. - 2021. - 40. - № 6. - P. 1309-1317. - 10.1007/s10096-021-04203-8 | |
| dc.identifier.doi | 10.1007/s10096-021-04203-8 | |
| dc.identifier.uri | https://www.doi.org/10.1007/s10096-021-04203-8 | |
| dc.identifier.uri | https://www.scopus.com/record/display.uri?eid=2-s2.0-85106680665&origin=resultslist | |
| dc.identifier.uri | https://openrepository.mephi.ru/handle/123456789/25395 | |
| dc.relation.ispartof | European Journal of Clinical Microbiology and Infectious Diseases | |
| dc.title | Automated Western immunoblotting detection of anti-SARS-CoV-2 serum antibodies | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| oaire.citation.issue | 6 | |
| oaire.citation.volume | 40 |