The SARS-CoV2 envelope differs from host cells, exposes procoagulant lipids, and is disrupted in vivo by oral rinses.

CPC aminophospholipids cetylpyridinium chloride clinical trials coagulation inflammation lipidomics mouthwash phospholipids virology

Journal

Journal of lipid research
ISSN: 1539-7262
Titre abrégé: J Lipid Res
Pays: United States
ID NLM: 0376606

Informations de publication

Date de publication:
06 2022
Historique:
received: 12 02 2022
revised: 23 03 2022
accepted: 04 04 2022
pubmed: 19 4 2022
medline: 29 6 2022
entrez: 18 4 2022
Statut: ppublish

Résumé

The lipid envelope of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an essential component of the virus; however, its molecular composition is undetermined. Addressing this knowledge gap could support the design of antiviral agents as well as further our understanding of viral-host protein interactions, infectivity, pathogenicity, and innate immune system clearance. Lipidomics revealed that the virus envelope comprised mainly phospholipids (PLs), with some cholesterol and sphingolipids, and with cholesterol/phospholipid ratio similar to lysosomes. Unlike cellular membranes, procoagulant amino-PLs were present on the external side of the viral envelope at levels exceeding those on activated platelets. Accordingly, virions directly promoted blood coagulation. To investigate whether these differences could enable selective targeting of the viral envelope in vivo, we tested whether oral rinses containing lipid-disrupting chemicals could reduce infectivity. Products containing PL-disrupting surfactants (such as cetylpyridinium chloride) met European virucidal standards in vitro; however, components that altered the critical micelle concentration reduced efficacy, and products containing essential oils, povidone-iodine, or chlorhexidine were ineffective. This result was recapitulated in vivo, where a 30-s oral rinse with cetylpyridinium chloride mouthwash eliminated live virus in the oral cavity of patients with coronavirus disease 19 for at least 1 h, whereas povidone-iodine and saline mouthwashes were ineffective. We conclude that the SARS-CoV-2 lipid envelope i) is distinct from the host plasma membrane, which may enable design of selective antiviral approaches; ii) contains exposed phosphatidylethanolamine and phosphatidylserine, which may influence thrombosis, pathogenicity, and inflammation; and iii) can be selectively targeted in vivo by specific oral rinses.

Identifiants

pubmed: 35436499
pii: S0022-2275(22)00041-4
doi: 10.1016/j.jlr.2022.100208
pmc: PMC9010312
pii:
doi:

Substances chimiques

Antiviral Agents 0
Lipids 0
Mouthwashes 0
RNA, Viral 0
Povidone-Iodine 85H0HZU99M
Cetylpyridinium CUB7JI0JV3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

100208

Subventions

Organisme : Medical Research Council
ID : MR/S00971X/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest Venture Life Group plc and Johnson & Johnson provided information on mouthwash formulations employed in the in vitro study. Venture Life Group partfunded the clinical study but had no input in study design, data analysis, or drafting of the article. The authors declare that they have no conflicts of interest with the contents of this article.

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Auteurs

Zack Saud (Z)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Victoria J Tyrrell (VJ)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Andreas Zaragkoulias (A)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Majd B Protty (MB)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Evelina Statkute (E)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Anzelika Rubina (A)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Kirsten Bentley (K)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Daniel A White (DA)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Patricia Dos Santos Rodrigues (PDS)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Robert C Murphy (RC)

Department of Pharmacology, University of Colorado Denver, Aurora, CO, USA.

Harald Köfeler (H)

Core Facility Mass Spectrometry, Medical University of Graz, Graz, Austria.

William J Griffiths (WJ)

Medical School, Swansea University, Swansea, United Kingdom.

Jorge Alvarez-Jarreta (J)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom.

Richard William Brown (RW)

ENT Department, Betsi Cadwaladr University Health Board, Wrexham Maelor Hospital, Wrexham, United Kingdom.

Robert G Newcombe (RG)

Division of Population Medicine, School of Medicine, Cardiff University, Cardiff, United Kingdom.

James Heyman (J)

Division of Surgery, Cardiff and Vale University Health Board, Cardiff, United Kingdom.

Manon Pritchard (M)

Advanced Therapies Group, School of Dentistry, Cardiff University, Cardiff, United Kingdom.

Robert Wj Mcleod (RW)

Division of Surgery, Cardiff and Vale University Health Board, Cardiff, United Kingdom.

Arvind Arya (A)

ENT Department, Betsi Cadwaladr University Health Board, Wrexham Maelor Hospital, Wrexham, United Kingdom.

Ceri-Ann Lynch (CA)

Anaesthetics and Critical Care Directorate, Cwm Taf University Health Board, Royal Glamorgan Hospital, Llantrisant, United Kingdom.

David Owens (D)

Division of Surgery, Cardiff and Vale University Health Board, Cardiff, United Kingdom.

P Vince Jenkins (PV)

Haemostasis Diagnosis and Research, University Hospital Wales, Cardiff, United Kingdom.

Niklaas J Buurma (NJ)

Physical Organic Chemistry Centre, School of Chemistry, Cardiff University, Cardiff, United Kingdom.

Valerie B O'Donnell (VB)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom. Electronic address: o-donnellvb@cardiff.ac.uk.

David W Thomas (DW)

Advanced Therapies Group, School of Dentistry, Cardiff University, Cardiff, United Kingdom. Electronic address: thomasdw2@cardiff.ac.uk.

Richard J Stanton (RJ)

Division of Infection & Immunity, School of Medicine, Cardiff University, Cardiff, United Kingdom. Electronic address: StantonRJ@cardiff.ac.uk.

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