HTCC: Broad Range Inhibitor of Coronavirus Entry

PLoS One. 2016 Jun 1;11(6):e0156552. doi: 10.1371/journal.pone.0156552. eCollection 2016.

Abstract

To date, six human coronaviruses have been known, all of which are associated with respiratory infections in humans. With the exception of the highly pathogenic SARS and MERS coronaviruses, human coronaviruses (HCoV-NL63, HCoV-OC43, HCoV-229E, and HCoV-HKU1) circulate worldwide and typically cause the common cold. In most cases, infection with these viruses does not lead to severe disease, although acute infections in infants, the elderly, and immunocompromised patients may progress to severe disease requiring hospitalization. Importantly, no drugs against human coronaviruses exist, and only supportive therapy is available. Previously, we proposed the cationically modified chitosan, N-(2-hydroxypropyl)-3-trimethylammonium chitosan chloride (HTCC), and its hydrophobically-modified derivative (HM-HTCC) as potent inhibitors of the coronavirus HCoV-NL63. Here, we show that HTCC inhibits interaction of a virus with its receptor and thus blocks the entry. Further, we demonstrate that HTCC polymers with different degrees of substitution act as effective inhibitors of all low-pathogenic human coronaviruses.

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology*
  • Cell Line
  • Chitosan / analogs & derivatives*
  • Chitosan / pharmacology
  • Coronavirus / drug effects
  • Coronavirus / physiology*
  • Humans
  • Macaca mulatta
  • Membrane Fusion / drug effects*
  • Quaternary Ammonium Compounds / pharmacology*
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • N-(2-hydroxypropyl)-3-trimethylammonium chitosan
  • Quaternary Ammonium Compounds
  • Chitosan

Grants and funding

This work was supported by the grant "Evaluation of anticoronal compounds" from the Unilab LP (966 Hungford Dr. Ste. 3B, Rockville, MD 20850, USA) (KS and KP), by the LIDER grant from the National Centre for Research and Development (Lider/27/55/L-2/10/2011) (KP), and by grants from the National Science Center (UMO-657 2012/07/E/NZ6/01712 and UMO-2012/07/N/NZ6/02955) (KP and AM, respectively). KP would like to acknowledge networking contribution by the COST Action CM1407 “Challenging organic syntheses inspired by nature - from natural products chemistry to drug discovery”. The Faculty of Biochemistry, Biophysics and Biotechnology of the Jagiellonian University is a beneficiary of the structural funds from the European Union (grant No: POIG.02.01.00-12-064/08 – “Molecular biotechnology for health”). Faculty of Biochemistry, Biophysics and Biotechnology of the Jagiellonian University is a partner of the Leading National Research Center supported by the Ministry of Science and Higher Education of the Republic of Poland. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.