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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...

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Autores principales: Wang, Wenbo, Li, Qianqian, Wu, Jiajing, Hu, Yu, Wu, Gang, Yu, Chuanfei, Xu, Kangwei, Liu, Xumei, Wang, Qihui, Huang, Weijin, Wang, Lan, Wang, Youchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
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.
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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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