A systematic analysis of anthocyanins inhibiting human, murine, and equine herpesviruses.

Anthocyanins Aristotelia chilensis Equine herpesvirus Human herpesviruses

Journal

Phytomedicine : international journal of phytotherapy and phytopharmacology
ISSN: 1618-095X
Titre abrégé: Phytomedicine
Pays: Germany
ID NLM: 9438794

Informations de publication

Date de publication:
25 Dec 2023
Historique:
received: 14 08 2023
revised: 22 11 2023
accepted: 25 12 2023
medline: 9 1 2024
pubmed: 9 1 2024
entrez: 8 1 2024
Statut: aheadofprint

Résumé

Herpesviruses are common animal and human pathogens that cause severe health problems in children, immunocompromised patients, and infected animals with a host range from fish to mammals. Anthocyanin-containing plant extracts have been described as potent antivirals, which might cause fewer harmful side effects than direct-acting antivirals. Here, we report that an extract of Aristotelia chilensis (Molina) Stuntz (Elaeocarpaceae) (MBE) with a high content of the anthocyanin delphinidin suppresses lytic replication of equine, murine and human herpesviruses of replication in vitro. We treated cultured cells with MBE and purified individual anthocyanins present in the extract to determine the most active compound at different concentrations. We subsequently infected the cultures with human herpesviruses 1 (HSV-1) or 8 (HHV-8), murine cytomegalovirus (CMV), or equine herpesviruses 1 (EHV-1) and determined the number of infected cells and viral infectivity. MBE inhibited the HSV-1, murine CMV, and EHV-1 by up to 2 orders of magnitude. In the presence of the stabilizing randomly methylated-beta-cyclodextrin, the inhibitory concentration could be lowered significantly. We identified delphinidin as an active antiviral compound and showed that the non-glycosylated delphinidin solved and stabilized with sulfobutylether-beta-cyclodextrin allowed usage of approximately 50 times lower concentrations. Glycosylated delphinidin derivatives were identified as active antiviral compounds of MBE. This suggests that plant extracts rich in delphinidin-anthocyanins have potent antiviral properties that could be used in treatment and prevention.

Sections du résumé

BACKGROUND BACKGROUND
Herpesviruses are common animal and human pathogens that cause severe health problems in children, immunocompromised patients, and infected animals with a host range from fish to mammals. Anthocyanin-containing plant extracts have been described as potent antivirals, which might cause fewer harmful side effects than direct-acting antivirals. Here, we report that an extract of Aristotelia chilensis (Molina) Stuntz (Elaeocarpaceae) (MBE) with a high content of the anthocyanin delphinidin suppresses lytic replication of equine, murine and human herpesviruses of replication in vitro.
METHODS METHODS
We treated cultured cells with MBE and purified individual anthocyanins present in the extract to determine the most active compound at different concentrations. We subsequently infected the cultures with human herpesviruses 1 (HSV-1) or 8 (HHV-8), murine cytomegalovirus (CMV), or equine herpesviruses 1 (EHV-1) and determined the number of infected cells and viral infectivity.
RESULTS RESULTS
MBE inhibited the HSV-1, murine CMV, and EHV-1 by up to 2 orders of magnitude. In the presence of the stabilizing randomly methylated-beta-cyclodextrin, the inhibitory concentration could be lowered significantly. We identified delphinidin as an active antiviral compound and showed that the non-glycosylated delphinidin solved and stabilized with sulfobutylether-beta-cyclodextrin allowed usage of approximately 50 times lower concentrations.
CONCLUSION CONCLUSIONS
Glycosylated delphinidin derivatives were identified as active antiviral compounds of MBE. This suggests that plant extracts rich in delphinidin-anthocyanins have potent antiviral properties that could be used in treatment and prevention.

Identifiants

pubmed: 38190783
pii: S0944-7113(23)00672-4
doi: 10.1016/j.phymed.2023.155314
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

155314

Informations de copyright

Copyright © 2023 Elsevier GmbH. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Valeria Roll (V)

Julius-Maximilians-University of Würzburg, Institute for Virology and Immunobiology, Versbacher Strasse 7, 97078 Würzburg, Germany.

Viktoria Diesendorf (V)

Julius-Maximilians-University of Würzburg, Institute for Virology and Immunobiology, Versbacher Strasse 7, 97078 Würzburg, Germany.

Norbert Roewer (N)

Universitätsklinikum Würzburg, Josef-Schneider-Str. 2, 97080 Würzburg, Germany.

Azza Abdelgawad (A)

Freie Universität Berlin, Institut für Virologie, Robert von Ostertag-Str. 7, 14163 Berlin, Germany.

Joachim Roewer (J)

Dermatologikum Hamburg, Stephansplatz 5, 20354 Hamburg, Germany.

Jakob Trimpert (J)

Freie Universität Berlin, Institut für Virologie, Robert von Ostertag-Str. 7, 14163 Berlin, Germany.

Jochen Bodem (J)

Julius-Maximilians-University of Würzburg, Institute for Virology and Immunobiology, Versbacher Strasse 7, 97078 Würzburg, Germany. Electronic address: jochen.bodem@uni-wuerzburg.de.

Classifications MeSH