Reference | ||
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Reference Type | Literature | IEDB_Reference:1039261 |
Title | Immunoreactive peptide maps of SARS-CoV-2. | |
Authors | Nischay Mishra; Xi Huang; Shreyas Joshi; Cheng Guo; James Ng; Riddhi Thakkar; Yongjian Wu; Xin Dong; Qianlin Li; Richard S Pinapati; Eric Sullivan; Adrian Caciula; Rafal Tokarz; Thomas Briese; Jiahai Lu; W Ian Lipkin | |
Affiliations | Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY, USA. nm2641@cumc.columbia.edu; Sun Yat-sen University, Guangzhou, Guangdong Province, China; Center for Infection and Immunity, Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong Province, China; School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong Province, China; Nimble Therapeutics Inc, Madison, WI, USA; Sun Yat-sen University, Guangzhou, Guangdong Province, China. lujiahai@mail.sysu.edu.cn; School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong Province, China. lujiahai@mail.sysu.edu.cn; Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY, USA. wil2001@cumc.columbia.edu. | |
Journal | Commun Biol | |
Year | 2021 | |
Abstract | Serodiagnosis of SARS-CoV-2 infection is impeded by immunological cross-reactivity among the human coronaviruses (HCoVs): SARS-CoV-2, SARS-CoV-1, MERS-CoV, OC43, 229E, HKU1, and NL63. Here we report the identification of humoral immune responses to SARS-CoV-2 peptides that may enable discrimination between exposure to SARS-CoV-2 and other HCoVs. We used a high-density peptide microarray and plasma samples collected at two time points from 50 subjects with SARS-CoV-2 infection confirmed by qPCR, samples collected in 2004-2005 from 11 subjects with IgG antibodies to SARS-CoV-1, 11 subjects with IgG antibodies to other seasonal human coronaviruses (HCoV), and 10 healthy human subjects. Through statistical modeling with linear regression and multidimensional scaling we identified specific peptides that were reassembled to identify 29 linear SARS-CoV-2 epitopes that were immunoreactive with plasma from individuals who had asymptomatic, mild or severe SARS-CoV-2 infections. Larger studies will be required to determine whether these peptides may be useful in serodiagnostics. | |
Curation Last Updated | 2025-03-25 21:53:15 |
Epitope | ||
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Epitope ID | 1528356 | IEDB_epitope:1528356 |
Chemical Type | Linear peptide | |
Linear Sequence | VRDKGALEKFMS | |
Source Molecule Name | ORF1ab [Middle East respiratory syndrome-related coronavirus] | |
Source Organism | Middle East respiratory syndrome-related coronavirus (MERS coronavirus) | |
Starting Position | 6580 | |
Ending Position | 6591 |
Epitope Reference Details | ||
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Epitope Structure Defines | Epitope containing region/antigenic site | |
Epitope Name | VRDKGALEKFMS | |
Location of Data in Reference | Supplementary Data 1 |
Immunization | ||
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Host Organism | Homo sapiens (human) |
Host Details | ||
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Host Geolocation | China |
1st In Vivo Process | ||
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In Vivo Process Type | Occurrence of infectious disease | |
Disease State | COVID-19 | |
Disease Stage | Acute/Recent onset; | OGMS:0000094 |
1st Immunogen | ||
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Epitope Relation | Taxonomic Sibling | |
Object Type | Organism | |
Organism | SARS-CoV2 |
B Cell Assay | ||
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Qualitative Measurement | Negative | |
Method/Technique | microarray | |
Measurement of | qualitative binding |
Assayed Antibody | ||
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Assayed Antibody Source Material | Serum | |
Assayed Antibody Immunoglobulin Domain | Entire Antibody | |
Assayed Antibody Purification Status | Polyclonal | |
Assayed Antibody Heavy Chain Type | IgM |
Antigen | ||
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Epitope Relation | Epitope | |
Chemical Type | Linear peptide | |
Linear Sequence | VRDKGALEKFMS | |
Source Molecule Name | ORF1ab [Middle East respiratory syndrome-related coronavirus] | |
Source Organism | Middle East respiratory syndrome-related coronavirus (MERS coronavirus) | |
Starting Position | 6580 | |
Ending Position | 6591 |
Assay Reference Details | ||
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Location of Assay Data in Reference | Supplementary Data 2 |