Next Article in Journal
Functional Properties and Sustainability Improvement of Sourdough Bread by Lactic Acid Bacteria
Next Article in Special Issue
Combination Regimens of Favipiravir Plus Interferon Alpha Inhibit Chikungunya Virus Replication in Clinically Relevant Human Cell Lines
Previous Article in Journal
Chemically Mediated Microbial “Gardening” Capacity of a Seaweed Holobiont Is Dynamic
Previous Article in Special Issue
Identification of an Antiviral Compound from the Pandemic Response Box that Efficiently Inhibits SARS-CoV-2 Infection In Vitro
Open AccessCommunication

SARS-CoV-2 Inhibition by Sulfonated Compounds

1
Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland
2
Institute of Virology and Immunology (IVI), Länggassstrasse 122, 3012 Bern, Switzerland
3
Institute for Infectious Diseases, University of Bern, Hochschulstrasse 6, 3012 Bern, Switzerland
4
Department of Microbiology and Molecular Medicine, University of Geneva, 1211 Geneve, Switzerland
5
Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland
*
Author to whom correspondence should be addressed.
These authors contributed equally.
Microorganisms 2020, 8(12), 1894; https://doi.org/10.3390/microorganisms8121894
Received: 30 October 2020 / Revised: 26 November 2020 / Accepted: 28 November 2020 / Published: 30 November 2020
(This article belongs to the Special Issue Recent Advances in Antivirals for Emerging Viruses)
Severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) depends on angiotensin converting enzyme 2 (ACE2) for cellular entry, but it might also rely on attachment receptors such as heparan sulfates. Several groups have recently demonstrated an affinity of the SARS-CoV2 spike protein for heparan sulfates and a reduced binding to cells in the presence of heparin or heparinase treatment. Here, we investigated the inhibitory activity of several sulfated and sulfonated molecules, which prevent interaction with heparan sulfates, against vesicular stomatitis virus (VSV)-pseudotyped-SARS-CoV-2 and the authentic SARS-CoV-2. Sulfonated cyclodextrins and nanoparticles that have recently shown broad-spectrum non-toxic virucidal activity against many heparan sulfates binding viruses showed inhibitory activity in the micromolar and nanomolar ranges, respectively. In stark contrast with the mechanisms that these compounds present for these other viruses, the inhibition against SARS-CoV-2 was found to be simply reversible. View Full-Text
Keywords: SARS-CoV-2; antiviral; heparan sulfates; attachment inhibitor SARS-CoV-2; antiviral; heparan sulfates; attachment inhibitor
Show Figures

Figure 1

MDPI and ACS Style

Gasbarri, M.; V’kovski, P.; Torriani, G.; Thiel, V.; Stellacci, F.; Tapparel, C.; Cagno, V. SARS-CoV-2 Inhibition by Sulfonated Compounds. Microorganisms 2020, 8, 1894. https://doi.org/10.3390/microorganisms8121894

AMA Style

Gasbarri M, V’kovski P, Torriani G, Thiel V, Stellacci F, Tapparel C, Cagno V. SARS-CoV-2 Inhibition by Sulfonated Compounds. Microorganisms. 2020; 8(12):1894. https://doi.org/10.3390/microorganisms8121894

Chicago/Turabian Style

Gasbarri, Matteo; V’kovski, Philip; Torriani, Giulia; Thiel, Volker; Stellacci, Francesco; Tapparel, Caroline; Cagno, Valeria. 2020. "SARS-CoV-2 Inhibition by Sulfonated Compounds" Microorganisms 8, no. 12: 1894. https://doi.org/10.3390/microorganisms8121894

Find Other Styles
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Search more from Scilit
 
Search
Back to TopTop