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Distinct antibody repertoires against endemic human coronaviruses in children and adults
Taushif Khan, … , Mohammad R. Hasan, Nico Marr
Taushif Khan, … , Mohammad R. Hasan, Nico Marr
Published January 26, 2021
Citation Information: JCI Insight. 2021;6(4):e144499. https://doi.org/10.1172/jci.insight.144499.
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Research Article Immunology Infectious disease

Distinct antibody repertoires against endemic human coronaviruses in children and adults

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Abstract

Four endemic human coronaviruses (HCoVs) are commonly associated with acute respiratory infection in humans. B cell responses to these “common cold” viruses remain incompletely understood. Here we report a comprehensive analysis of CoV-specific antibody repertoires in 231 children and 1168 adults using phage immunoprecipitation sequencing. Seroprevalence of antibodies against endemic HCoVs ranged between approximately 4% and 27% depending on the species and cohort. We identified at least 136 novel linear B cell epitopes. Antibody repertoires against endemic HCoVs were qualitatively different between children and adults in that anti-HCoV IgG specificities more frequently found among children targeted functionally important and structurally conserved regions of the spike, nucleocapsid, and matrix proteins. Moreover, antibody specificities targeting the highly conserved fusion peptide region and S2′ cleavage site of the spike protein were broadly cross-reactive with peptides of epidemic human and nonhuman coronaviruses. In contrast, an acidic tandem repeat in the N-terminal region of the Nsp3 subdomain of the HCoV-HKU1 polyprotein was the predominant target of antibody responses in adult donors. Our findings shed light on the dominant species-specific and pan-CoV target sites of human antibody responses to coronavirus infection, thereby providing important insights for the development of prophylactic or therapeutic monoclonal antibodies and vaccine design.

Authors

Taushif Khan, Mahbuba Rahman, Fatima Al Ali, Susie S. Y. Huang, Manar Ata, Qian Zhang, Paul Bastard, Zhiyong Liu, Emmanuelle Jouanguy, Vivien Béziat, Aurélie Cobat, Gheyath K. Nasrallah, Hadi M. Yassine, Maria K. Smatti, Amira Saeed, Isabelle Vandernoot, Jean-Christophe Goffard, Guillaume Smits, Isabelle Migeotte, Filomeen Haerynck, Isabelle Meyts, Laurent Abel, Jean-Laurent Casanova, Mohammad R. Hasan, Nico Marr

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Figure 3

Antigenic regions and predicted antibody binding sites of the S protein.

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Antigenic regions and predicted antibody binding sites of the S protein....
(A) Schematic representation of the S protein of SARS-CoV (UniProtKB entry P59594). Proteolytic cleavage sites are marked with arrows. FP, fusion peptide; HR, heptad repeats; TMD, transmembrane domain. (B) Overview of a multiple sequence alignment of immunodominant peptides with the full-length protein sequences of various alpha- and beta-CoVs (top). Row labels indicate the UniProtKB sequence identifier, start and end positions of enriched peptides (in parentheses), names of the organisms, and cluster numbers (in square brackets). Peptides for which differential enrichment between children and adults were statistically significant (P ≤ 0.005, Fisher’s exact test) and ORs were at least 2 are indicated with an asterisk. Colors indicate protein domains as shown in A, as well as predicted (pink) (42) and experimentally validated (purple) (56) linear SARS-CoV-2 B cell epitopes. Vertical dashed lines indicate boundaries of regions shown in C–E. The line plot (bottom) shows the mean BepiPred score (blue line) and SD (shaded) for the prediction of linear B cell epitopes among endemic HCoVs. The significance threshold of 0.55 has been marked with a dashed red line. (C–E) Selected regions of the multiple sequence alignment encompassing the N-terminal region of the receptor binding domain (C), the S1/S2 cleavage site (D), and the S2′ cleavage site (E). Amino acid positions on top are shown for UniProtKB entry P59594. Amino acids are marked in color to indicate the level of sequence identity (blue), the proteolytic cleavage sites (black), and linear SARS-CoV-2 B cell epitopes as shown in B. The full sequence alignment is shown in Supplemental Figure 5A.
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