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Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein
Emerging and re-emerging viral infections have been an important public health problem in recent years. We focused our attention on Toscana virus (TOSV), an emergent neurotropic negative-strand RNA virus of the Phenuiviridae family. The mechanisms of protection against phlebovirus natural infection...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402642/ https://www.ncbi.nlm.nih.gov/pubmed/34452049 http://dx.doi.org/10.3390/vaccines9080924 |
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author | Gandolfo, Claudia Prathyumn, Shibily Terrosi, Chiara Anichini, Gabriele Gori Savellini, Gianni Corti, Davide Bracci, Luisa Lanzavecchia, Antonio Roman-Sosa, Gleyder Cusi, Maria Grazia |
author_facet | Gandolfo, Claudia Prathyumn, Shibily Terrosi, Chiara Anichini, Gabriele Gori Savellini, Gianni Corti, Davide Bracci, Luisa Lanzavecchia, Antonio Roman-Sosa, Gleyder Cusi, Maria Grazia |
author_sort | Gandolfo, Claudia |
collection | PubMed |
description | Emerging and re-emerging viral infections have been an important public health problem in recent years. We focused our attention on Toscana virus (TOSV), an emergent neurotropic negative-strand RNA virus of the Phenuiviridae family. The mechanisms of protection against phlebovirus natural infection are not known; however, it is supposed that a virus-neutralizing antibody response against viral glycoproteins would be useful to block the first stages of infection. By using an improved memory B cell immortalization method, we obtained a panel of human mAbs which reacted with TOSV antigens. We identified three epitopes of TOSV Gn glycoproteins by neutralizing mAbs using synthetic peptide arrays on membrane support (SPOT synthesis). These epitopes, separated in primary structure, might be exposed near one another as a conformational epitope in their native structure. In vivo studies were conducted to evaluate the humoral response elicited in mice immunized with the identified peptides. The results underlined the hypothesis that the first two peptides located in the NH(2) terminus could form a conformational epitope, while the third, located near the transmembrane sequence in the carboxyl terminus, was necessary to strengthen neutralizing activity. Our results emphasize the importance of identifying neutralizing epitopes shared among the various phleboviruses, which could be exploited for the development of a potential epitope-based diagnostic assay or a polyvalent protective vaccine against different phleboviruses. |
format | Online Article Text |
id | pubmed-8402642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84026422021-08-29 Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein Gandolfo, Claudia Prathyumn, Shibily Terrosi, Chiara Anichini, Gabriele Gori Savellini, Gianni Corti, Davide Bracci, Luisa Lanzavecchia, Antonio Roman-Sosa, Gleyder Cusi, Maria Grazia Vaccines (Basel) Article Emerging and re-emerging viral infections have been an important public health problem in recent years. We focused our attention on Toscana virus (TOSV), an emergent neurotropic negative-strand RNA virus of the Phenuiviridae family. The mechanisms of protection against phlebovirus natural infection are not known; however, it is supposed that a virus-neutralizing antibody response against viral glycoproteins would be useful to block the first stages of infection. By using an improved memory B cell immortalization method, we obtained a panel of human mAbs which reacted with TOSV antigens. We identified three epitopes of TOSV Gn glycoproteins by neutralizing mAbs using synthetic peptide arrays on membrane support (SPOT synthesis). These epitopes, separated in primary structure, might be exposed near one another as a conformational epitope in their native structure. In vivo studies were conducted to evaluate the humoral response elicited in mice immunized with the identified peptides. The results underlined the hypothesis that the first two peptides located in the NH(2) terminus could form a conformational epitope, while the third, located near the transmembrane sequence in the carboxyl terminus, was necessary to strengthen neutralizing activity. Our results emphasize the importance of identifying neutralizing epitopes shared among the various phleboviruses, which could be exploited for the development of a potential epitope-based diagnostic assay or a polyvalent protective vaccine against different phleboviruses. MDPI 2021-08-19 /pmc/articles/PMC8402642/ /pubmed/34452049 http://dx.doi.org/10.3390/vaccines9080924 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gandolfo, Claudia Prathyumn, Shibily Terrosi, Chiara Anichini, Gabriele Gori Savellini, Gianni Corti, Davide Bracci, Luisa Lanzavecchia, Antonio Roman-Sosa, Gleyder Cusi, Maria Grazia Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title | Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title_full | Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title_fullStr | Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title_full_unstemmed | Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title_short | Identification of a Neutralizing Epitope on TOSV Gn Glycoprotein |
title_sort | identification of a neutralizing epitope on tosv gn glycoprotein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402642/ https://www.ncbi.nlm.nih.gov/pubmed/34452049 http://dx.doi.org/10.3390/vaccines9080924 |
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