Capture and neutralization of SARS-CoV-2 and influenza virus by algae-derived lectins with high-mannose and core fucose specificities.


Journal

Microbiology and immunology
ISSN: 1348-0421
Titre abrégé: Microbiol Immunol
Pays: Australia
ID NLM: 7703966

Informations de publication

Date de publication:
Jul 2023
Historique:
revised: 02 05 2023
received: 09 12 2022
accepted: 14 05 2023
medline: 4 7 2023
pubmed: 30 5 2023
entrez: 29 5 2023
Statut: ppublish

Résumé

We first investigated the interactions between several algae-derived lectins and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). We created lectin columns using high-mannose (HM)-type glycan-specific lectins OAA and KAA-1 or core fucose-specific lectin hypninA-2 and conducted binding experiments with SARS-CoV-2. The results showed that these lectins were capable of binding to the virus. Furthermore, when examining the neutralization ability of nine different lectins, it was found that KAA-1, ESA-2, and hypninA-2 were effective in neutralizing SARS-CoV-2. In competitive inhibition experiments with glycoproteins, neutralization was confirmed to occur through HM-type or core fucose-type glycans. However, neutralization was not observed with other lectins, such as OAA. This trend of KAA-1 and ESA-2 having the neutralizing ability and OAA not having it was also similar to influenza viruses. Electron microscopy observations revealed that KAA-1 and hypninA-2 strongly aggregated SARS-CoV-2 particles, while OAA showed a low degree of aggregation. It is believed that the neutralization of SARS-CoV-2 involves multiple factors, such as glycan attachment sites on the S protein, the size of lectins, and their propensity to aggregate, which cause inhibition of receptor binding or aggregation of virus particles. This study demonstrated that several algae-derived lectins could neutralize SARS-CoV-2 and that lectin columns can effectively recover and concentrate the virus.

Identifiants

pubmed: 37248051
doi: 10.1111/1348-0421.13082
doi:

Substances chimiques

Mannose PHA4727WTP
Fucose 28RYY2IV3F
Lectins 0
Mannose-Binding Lectins 0
Polysaccharides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

334-344

Subventions

Organisme : Government-Academia Collaboration of Hiroshima Prefecture
Organisme : Japan Science and Technology Agency
ID : JPMJSP2132
Organisme : Otsuka Toshimi Scholarship Foundation
Organisme : Japan Agency for Medical Research and Development
ID : JP20fk0108453
Organisme : Japan Agency for Medical Research and Development
ID : JP20he0622011
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0108550
Organisme : Japan Agency for Medical Research and Development
ID : JP21fk0108558

Informations de copyright

© 2023 The Societies and John Wiley & Sons Australia, Ltd.

Références

Dhama K, Khan S, Tiwari R, et al. Coronavirus disease 2019-COVID-19. Clin Microbiol Rev. 2020;33:e00028-20. https://doi.org/10.1128/CMR.00028-20
Ke Z, Oton J, Qu K, et al. Structures and distributions of SARS-CoV-2 spike proteins on intact virions. Nature. 2020;588:498-502. https://doi.org/10.1038/s41586-020-2665-2
Hoffmann M, Kleine-Weber H, Schroeder S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell. 2020;181:271-80.e8. https://doi.org/10.1016/j.cell.2020.02.052
Walls AC, Park YJ, Tortorici MA, Wall A, Mcguire AT, Veesler D. Structure, function, and antigenicity of the SARS-CoV-2 spike glycoprotein. Cell. 2020;181:281-92. https://doi.org/10.1016/j.cell.2020.02.058
Shajahan A, Supekar NT, Gleinich AS, Azadi P. Deducing the N- and O-glycosylation profile of the spike protein of novel coronavirus SARS-CoV-2. Glycobiology. 2020;30:981-8. https://doi.org/10.1093/glycob/cwaa042
Watanabe Y, Allen JD, Wrapp D, Mclellan JS, Crispin M. Site-specific glycan analysis of the SARS-CoV-2 spike. Science. 2020;369:330-3. https://doi.org/10.1126/science.abb9983
Zhang Y, Zhao W, Mao Y, et al. Site-specific N-glycosylation characterization of recombinant SARS-CoV-2 spike proteins. Mol Cell Proteomics. 2021;20:100058. https://doi.org/10.1074/mcp.RA120.002295
Grant OC, Montgomery D, Ito K, Woods RJ. Analysis of the SARS-CoV-2 spike protein glycan shield reveals implications for immune recognition. Sci Rep. 2020;10:14991. https://doi.org/10.1038/s41598-020-71748-7
Casalino L, Gaieb Z, Goldsmith JA, et al. Beyond shielding: the roles of glycans in the SARS-CoV-2 spike protein. ACS Cent Sci. 2020;6:1722-34. https://doi.org/10.1021/acscentsci.0c01056
Ahan RE, Hanifehnezhad A, Kehribar EŞ, et al. A highly potent SARS-CoV-2 blocking lectin protein. ACS Infect Dis. 2022;8:1253-64. https://doi.org/10.1021/acsinfecdis.2c00006
Cai Y, Xu W, Gu C, et al. Griffithsin with a broad-spectrum antiviral activity by binding glycans in viral glycoprotein exhibits strong synergistic effect in combination with a pan-coronavirus fusion inhibitor targeting SARS-CoV-2 spike S2 subunit. Virol Sin. 2020;35:857-60. https://doi.org/10.1007/s12250-020-00305-3
Liu YM, Shahed-Al-Mahmud M, Chen X, et al. A carbohydrate-binding protein from the edible lablab beans effectively blocks the infections of influenza viruses and SARS-CoV-2. Cell Rep. 2020;32:108016. https://doi.org/10.1016/j.celrep.2020.108016
Sarkar A, Paul S, Singh C, et al. A novel plant lectin, NTL-125, interferes with SARS-CoV-2 interaction with hACE2. Virus Res. 2022;315:198768. https://doi.org/10.1016/j.virusres.2022.198768
Sheehan SA, Hamilton KL, Retzbach EP, et al. Evidence that Maackia amurensis seed lectin (MASL) exerts pleiotropic actions on oral squamous cells with potential to inhibit SARS-CoV-2 infection and COVID-19 disease progression. Exp Cell Res. 2021;403:112594. https://doi.org/10.1016/j.yexcr.2021.112594
Wang W, Li Q, Wu J, et al. Lentil lectin derived from Lens culinaris exhibit broad antiviral activities against SARS-CoV-2 variants. Emerg Microbes Infect. 2021;10:1519-29. https://doi.org/10.1080/22221751.2021.1957720
Hirayama M, Shibata H, Imamura K, Sakaguchi T, Hori K. High-mannose specific lectin and its recombinants from a Carrageenophyta Kappaphycus alvarezii represent a potent anti-HIV activity through high-affinity binding to the viral envelope glycoprotein gp120. Mar Biotechnol. 2016;18:144-60. https://doi.org/10.1007/s10126-015-9677-1
Sato Y, Hirayama M, Morimoto K, Yamamoto N, Okuyama S, Hori K. High mannose-binding lectin with preference for the cluster of α1-2-mannose from the green alga Boodlea coacta is a potent entry inhibitor of HIV-1 and influenza viruses. J Biol Chem. 2011;286:19446-58. https://doi.org/10.1074/jbc.M110.216655
Sato Y, Morimoto K, Hirayama M, Hori K. High mannose-specific lectin (KAA-2) from the red alga Kappaphycus alvarezii potently inhibits influenza virus infection in a strain-independent manner. Biochem Biophys Res Commun. 2011;405:291-6. https://doi.org/10.1016/j.bbrc.2011.01.031
Sato Y, Morimoto K, Kubo T, et al. Entry inhibition of influenza viruses with high mannose binding lectin ESA-2 from the red alga Eucheuma serra through the recognition of viral hemagglutinin. Mar Drugs. 2015;13:3454-65. https://doi.org/10.3390/md13063454
Sato Y, Okuyama S, Hori K. Primary structure and carbohydrate binding specificity of a potent anti-HIV lectin isolated from the filamentous cyanobacterium Oscillatoria agardhii. J Biol Chem. 2007;282:11021-9. https://doi.org/10.1074/jbc.M701252200
Okuyama S, Nakamura-Tsuruta S, Tateno H, Hirabayashi J, Matsubara K, Hori K. Strict binding specificity of small-sized lectins from the red algaHypnea japonica for Core (α1-6) Fucosylated N-glycans. Biosci Biotechnol Biochem. 2009;73:912-20. https://doi.org/10.1271/bbb.80881
Hori K, Sato Y, Ito K, et al. Strict specificity for high-mannose type N-glycans and primary structure of a red alga Eucheuma serra lectin. Glycobiology. 2007;17:479-91. https://doi.org/10.1093/glycob/cwm007
Boyd MR, Gustafson KR, McMahon JB, et al. Discovery of cyanovirin-N, a novel human immunodeficiency virus-inactivating protein that binds viral surface envelope glycoprotein gp120: potential applications to microbicide development. Antimicrob Agents Chemother. 1997;41:1521-30. https://doi.org/10.1128/AAC.41.7.1521
Bewley CA. Solution structure of a Cyanovirin-N:Manα1-2Manα complex. Structure. 2001;9:931-40. https://doi.org/10.1016/s0969-2126(01)00653-0
Yamaguchi M, Ogawa T, Muramoto K, Kamio Y, Jimbo M, Kamiya H. Isolation and characterization of a mannan-binding lectin from the freshwater cyanobacterium (blue-green algae) Microcystis viridis. Biochem Biophys Res Commun. 1999;265:703-8. https://doi.org/10.1006/bbrc.1999.1749
Williams Jr. DC, Lee JY, Cai M. Crystal structures of the HIV-1 inhibitory cyanobacterial protein MVL free and bound to Man3GlcNAc2. J Biol Chem. 2005;280:29269-76. https://doi.org/10.1074/jbc.M504642200
Hori K, Matsubara K, Miyazawa K. Primary structures of two hemagglutinins from the marine red alga, Hypnea japonica. Biochim Biophys Acta. 2000;1474:226-36. https://doi.org/10.1016/s0304-4165(00)00008-8
Armstrong N, Lencastre AD, Gouaux E. A new protein folding screen: application to the ligand binding domains of a glutamate and kainate receptor and to lysozyme and carbonic anhydrase. Prot Sci. 1999;8:1475-83. https://doi.org/10.1110/ps.8.7.1475
Nomura T, Nazmul T, Yoshimoto R, Higashiura A, Oda K, Sakaguchi T. Ethanol susceptibility of SARS-CoV-2 and other enveloped viruses. Biocontrol Sci. 2021;26:177-80. https://doi.org/10.4265/bio.26.177
Matsuyama S, Nao N, Shirato K, et al. Enhanced isolation of SARS-CoV-2 by TMPRSS2-expressing cells. Proc Natl Acad Sci. 2020;117:7001-3. https://doi.org/10.1073/pnas.2002589117
Noma K, Kiyotani K, Kouchi H, et al. Endogenous protease-dependent replication of human influenza viruses in two MDCK cell lines. Arch Virol. 1998;143:1893-909. https://doi.org/10.1007/s007050050428
Ueda K, Kawabata R, Irie T, Nakai Y, Tohya Y, Sakaguchi T. Inactivation of pathogenic viruses by plant-derived tannins: strong effects of extracts from persimmon (Diospyros kaki) on a broad range of viruses. PLoS One. 2013;8:e55343. https://doi.org/10.1371/jornal.pone.0055343
Kitagawa H, Nomura T, Nazmul T, et al. Effectiveness of 222-nm ultraviolet light on disinfecting SARS-CoV-2 surface contamination. Am J Infect Control. 2021;49:299-301. https://doi.org/10.1016/j.ajic.2020.08.022
Yamasaki K, Adachi N, Ngwe Tun MM, et al. Core fucose-specific Pholiota squarrosa lectin (PhoSL) as a potent broad-spectrum inhibitor of SARS-CoV-2 infection. FEBS J. 2022;290:412-27. https://doi.org/10.1111/febs.16599
Barre A, Simplicien M, Benoist H, Van Damme EJM, Rougé P. Mannose-specific lectins from marine algae: diverse structural scaffolds associated to common virucidal and anti-cancer properties. Mar Drugs. 2019;17:440. https://doi.org/10.3390/md17080440
Barre A, Van Damme EJM, Klonjkowski B, et al. Legume lectins with different specificities as potential glycan probes for pathogenic enveloped viruses. Cells. 2022;11:339. https://doi.org/10.3390/cells11030339
Kitajima M, Ahmed W, Bibby K, et al. SARS-CoV-2 in wastewater: state of the knowledge and research needs. Sci Total Environ. 2020;739:139076. https://doi.org/10.1016/j.scitotenv.2020.139076
Panchal D, Prakash O, Bobde P, Pal S. SARS-CoV-2: sewage surveillance as an early warning system and challenges in developing countries. Environ Sci Pollut Res. 2021;28:22221-40. https://doi.org/10.1007/s11356-021-13170-8

Auteurs

Tanuza Nazmul (T)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Basirat M Lawal-Ayinde (BM)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Tomoko Morita (T)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Reiko Yoshimoto (R)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Akifumi Higashiura (A)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Akima Yamamoto (A)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Toshihito Nomura (T)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Department of Infectious Diseases, Hiroshima University Hospital, Hiroshima, Japan.

Yukiko Nakano (Y)

Laboratory of Marine Bioresource Chemistry, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Japan.

Makoto Hirayama (M)

Laboratory of Marine Bioresource Chemistry, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Japan.

Hiroshi Kurokawa (H)

Alps Alpine Co., Ltd, Tokyo, Japan.

Yasuyuki Kitamura (Y)

Alps Alpine Co., Ltd, Tokyo, Japan.

Kanji Hori (K)

Laboratory of Marine Bioresource Chemistry, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, Japan.

Takemasa Sakaguchi (T)

Department of Virology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH