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Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants
The spike (S) protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutated continuously and newly emerging variants escape from antibody-mediated neutralization raised great concern. S protein is heavily glycosylated and the glycosylation sites are relatively conserved, thus glyca...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330776/ https://www.ncbi.nlm.nih.gov/pubmed/34278967 http://dx.doi.org/10.1080/22221751.2021.1957720 |
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author | Wang, Wenbo Li, Qianqian Wu, Jiajing Hu, Yu Wu, Gang Yu, Chuanfei Xu, Kangwei Liu, Xumei Wang, Qihui Huang, Weijin Wang, Lan Wang, Youchun |
author_facet | Wang, Wenbo Li, Qianqian Wu, Jiajing Hu, Yu Wu, Gang Yu, Chuanfei Xu, Kangwei Liu, Xumei Wang, Qihui Huang, Weijin Wang, Lan Wang, Youchun |
author_sort | Wang, Wenbo |
collection | PubMed |
description | The spike (S) protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutated continuously and newly emerging variants escape from antibody-mediated neutralization raised great concern. S protein is heavily glycosylated and the glycosylation sites are relatively conserved, thus glycans on S protein surface could be a target for the development of anti-SARS-CoV-2 strategies against variants. Here, we collected 12 plant-derived lectins with different carbohydrate specificity and evaluated their anti-SARS-CoV-2 activity against mutant strains and epidemic variants using a pseudovirus-based neutralization assay. The Lens culinaris-derived lentil lectin which specifically bind to oligomannose-type glycans and GlcNAc at the non-reducing end terminus showed most potent and broad antiviral activity against a panel of mutant strains and variants, including the artificial mutants at N-/O-linked glycosylation site, natural existed amino acid mutants, as well as the epidemic variants B.1.1.7, B.1.351, and P.1. Lentil lectin also showed antiviral activity against SARS-CoV and MERS-CoV. We found lentil lectin could block the binding of ACE2 to S trimer and inhibit SARS-CoV-2 at the early steps of infection. Using structural information and determined N-glycan profile of S trimer, taking together with the carbohydrate specificity of lentil lectin, we provide a basis for the observed broad spectrum anti-SARS-CoV-2 activity. Lentil lectin showed weak haemagglutination activity at 1 mg/mL and no cytotoxicity activity, and no weight loss was found in single injection mouse experiment. This report provides the first evidence that lentil lectin strongly inhibit infection of SARS-COV-2 variants, which should provide valuable insights for developing future anti-SARS-CoV-2 strategies. |
format | Online Article Text |
id | pubmed-8330776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-83307762021-08-09 Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants Wang, Wenbo Li, Qianqian Wu, Jiajing Hu, Yu Wu, Gang Yu, Chuanfei Xu, Kangwei Liu, Xumei Wang, Qihui Huang, Weijin Wang, Lan Wang, Youchun Emerg Microbes Infect Research Article The spike (S) protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutated continuously and newly emerging variants escape from antibody-mediated neutralization raised great concern. S protein is heavily glycosylated and the glycosylation sites are relatively conserved, thus glycans on S protein surface could be a target for the development of anti-SARS-CoV-2 strategies against variants. Here, we collected 12 plant-derived lectins with different carbohydrate specificity and evaluated their anti-SARS-CoV-2 activity against mutant strains and epidemic variants using a pseudovirus-based neutralization assay. The Lens culinaris-derived lentil lectin which specifically bind to oligomannose-type glycans and GlcNAc at the non-reducing end terminus showed most potent and broad antiviral activity against a panel of mutant strains and variants, including the artificial mutants at N-/O-linked glycosylation site, natural existed amino acid mutants, as well as the epidemic variants B.1.1.7, B.1.351, and P.1. Lentil lectin also showed antiviral activity against SARS-CoV and MERS-CoV. We found lentil lectin could block the binding of ACE2 to S trimer and inhibit SARS-CoV-2 at the early steps of infection. Using structural information and determined N-glycan profile of S trimer, taking together with the carbohydrate specificity of lentil lectin, we provide a basis for the observed broad spectrum anti-SARS-CoV-2 activity. Lentil lectin showed weak haemagglutination activity at 1 mg/mL and no cytotoxicity activity, and no weight loss was found in single injection mouse experiment. This report provides the first evidence that lentil lectin strongly inhibit infection of SARS-COV-2 variants, which should provide valuable insights for developing future anti-SARS-CoV-2 strategies. Taylor & Francis 2021-08-01 /pmc/articles/PMC8330776/ /pubmed/34278967 http://dx.doi.org/10.1080/22221751.2021.1957720 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Wenbo Li, Qianqian Wu, Jiajing Hu, Yu Wu, Gang Yu, Chuanfei Xu, Kangwei Liu, Xumei Wang, Qihui Huang, Weijin Wang, Lan Wang, Youchun Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title | Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title_full | Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title_fullStr | Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title_full_unstemmed | Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title_short | Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants |
title_sort | lentil lectin derived from lens culinaris exhibit broad antiviral activities against sars-cov-2 variants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330776/ https://www.ncbi.nlm.nih.gov/pubmed/34278967 http://dx.doi.org/10.1080/22221751.2021.1957720 |
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