Production and characterization of chimeric SARS-CoV-2 antigens based on the capsid protein of cowpea chlorotic mottle virus
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The COVID-19 pandemic has highlighted the need for new vaccine platforms to rapidly develop solutions against emerging pathogens. In particular, some plant viruses offer several advantages for developing subunit vaccines, such as high expression rates in E. coli, high immunogenicity and safety, and absence of pre-immunity that could interfere with the vaccine%27s efficacy. Cowpea chlorotic mottle virus (CCMV) is a model system that has been extensively characterized, with key advantages for its use as an epitope carrier. In the present study, three relevant epitopes from the SARS-CoV-2 Spike protein were genetically inserted into the CCMV CP and expressed in E. coli cultures, resulting in the CCMV1, CCMV2, and CCMV3 chimeras. The recombinant CP mutants were purified from the formed inclusion bodies and refolded, and their immunogenicity as a subunit vaccine was assessed in BALB/c mice. The three mutants are immunogenic as they induce high IgG antibody titers that recognize the recombinant full-length S protein. This study supports the application of CCMV CP as an attractive carrier for the clinical evaluation of vaccine candidates against SARS-CoV-2. Furthermore, it suggests that VLPs assembled from these chimeric proteins could result in antigens with better immunogenicity. © 2022 Elsevier B.V.
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Chimeric protein; Humoral response; Plant virus ampicillin; angiotensin converting enzyme 2; antigen; capsid protein; chimeric protein; chloramphenicol; epitope; immunoglobulin G antibody; immunoglobulin G1; immunoglobulin G2a; subunit vaccine; virus spike protein; capsid protein; coronavirus spike glycoprotein; spike protein, SARS-CoV-2; animal experiment; animal model; Article; chimera; controlled study; coronavirus disease 2019; cowpea; cowpea chlorotic mottle virus; drug efficacy; enzyme linked immunosorbent assay; Escherichia coli; humoral immunity; immune response; immunization; immunoblotting; immunogenicity; mouse; nonhuman; pandemic; plant virus; polyacrylamide gel electrophoresis; prediction; protein expression; protein expression assay; protein structure; SARS-CoV-2 Delta; Severe acute respiratory syndrome coronavirus 2; Western blotting; animal; Bromovirus; chimera; genetics; human; metabolism; prevention and control; Animals; Bromovirus; Capsid Proteins; Chimera; COVID-19; Epitopes; Escherichia coli; Humans; Mice; Pandemics; SARS-CoV-2; Spike Glycoprotein, Coronavirus; Vaccines, Subunit
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