A defined anthocyanin mixture sourced from bilberry and black currant inhibits Measles virus and various herpesviruses.


Journal

BMC complementary medicine and therapies
ISSN: 2662-7671
Titre abrégé: BMC Complement Med Ther
Pays: England
ID NLM: 101761232

Informations de publication

Date de publication:
08 Jul 2022
Historique:
received: 18 08 2021
accepted: 29 06 2022
entrez: 8 7 2022
pubmed: 9 7 2022
medline: 14 7 2022
Statut: epublish

Résumé

Anthocyanin-containing plant extracts and carotenoids, such as astaxanthin, have been well-known for their antiviral and anti-inflammatory activity, respectively. We hypothesised that a mixture of Ribes nigrum L. (Grossulariaceae) (common name black currant (BC)) and Vaccinium myrtillus L. (Ericaceae) (common name bilberry (BL)) extracts (BC/BL) with standardised anthocyanin content as well as single plant extracts interfered with the replication of Measles virus and Herpesviruses in vitro. We treated cell cultures with BC/BL or defined single plant extracts, purified anthocyanins and astaxanthin in different concentrations and subsequently infected the cultures with the Measles virus (wild-type or vaccine strain Edmonston), Herpesvirus 1 or 8, or murine Cytomegalovirus. Then, we analysed the number of infected cells and viral infectivity and compared the data to non-treated controls. The BC/BL extract inhibited wild-type Measles virus replication, syncytia formation and cell-to-cell spread. This suppression was dependent on the wild-type virus-receptor-interaction since the Measles vaccine strain was unaffected by BC/BL treatment. Furthermore, the evidence was provided that the delphinidin-3-rutinoside chloride, a component of BC/BL, and purified astaxanthin, were effective anti-Measles virus compounds. Human Herpesvirus 1 and murine Cytomegalovirus replication was inhibited by BC/BL, single bilberry or black currant extracts, and the BC/BL component delphinidin-3-glucoside chloride. Additionally, we observed that BC/BL seemed to act synergistically with aciclovir. Moreover, BC/BL, the single bilberry and black currant extracts, and the BC/BL components delphinidin-3-glucoside chloride, cyanidin-3-glucoside, delphinidin-3-rutinoside chloride, and petunidin-3-galactoside inhibited human Herpesvirus 8 replication. Our data indicate that Measles viruses and Herpesviruses are differentially susceptible to a specific BC/BL mixture, single plant extracts, purified anthocyanins and astaxanthin. These compounds might be used in the prevention of viral diseases and in addition to direct-acting antivirals, such as aciclovir.

Sections du résumé

BACKGROUND BACKGROUND
Anthocyanin-containing plant extracts and carotenoids, such as astaxanthin, have been well-known for their antiviral and anti-inflammatory activity, respectively. We hypothesised that a mixture of Ribes nigrum L. (Grossulariaceae) (common name black currant (BC)) and Vaccinium myrtillus L. (Ericaceae) (common name bilberry (BL)) extracts (BC/BL) with standardised anthocyanin content as well as single plant extracts interfered with the replication of Measles virus and Herpesviruses in vitro.
METHODS METHODS
We treated cell cultures with BC/BL or defined single plant extracts, purified anthocyanins and astaxanthin in different concentrations and subsequently infected the cultures with the Measles virus (wild-type or vaccine strain Edmonston), Herpesvirus 1 or 8, or murine Cytomegalovirus. Then, we analysed the number of infected cells and viral infectivity and compared the data to non-treated controls.
RESULTS RESULTS
The BC/BL extract inhibited wild-type Measles virus replication, syncytia formation and cell-to-cell spread. This suppression was dependent on the wild-type virus-receptor-interaction since the Measles vaccine strain was unaffected by BC/BL treatment. Furthermore, the evidence was provided that the delphinidin-3-rutinoside chloride, a component of BC/BL, and purified astaxanthin, were effective anti-Measles virus compounds. Human Herpesvirus 1 and murine Cytomegalovirus replication was inhibited by BC/BL, single bilberry or black currant extracts, and the BC/BL component delphinidin-3-glucoside chloride. Additionally, we observed that BC/BL seemed to act synergistically with aciclovir. Moreover, BC/BL, the single bilberry and black currant extracts, and the BC/BL components delphinidin-3-glucoside chloride, cyanidin-3-glucoside, delphinidin-3-rutinoside chloride, and petunidin-3-galactoside inhibited human Herpesvirus 8 replication.
CONCLUSIONS CONCLUSIONS
Our data indicate that Measles viruses and Herpesviruses are differentially susceptible to a specific BC/BL mixture, single plant extracts, purified anthocyanins and astaxanthin. These compounds might be used in the prevention of viral diseases and in addition to direct-acting antivirals, such as aciclovir.

Identifiants

pubmed: 35804339
doi: 10.1186/s12906-022-03661-7
pii: 10.1186/s12906-022-03661-7
pmc: PMC9264518
doi:

Substances chimiques

Anthocyanins 0
Antiviral Agents 0
Chlorides 0
Plant Extracts 0
Acyclovir X4HES1O11F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

181

Informations de copyright

© 2022. The Author(s).

Références

Mar Drugs. 2018 Nov 02;16(11):
pubmed: 30400141
J Virol. 2007 Mar;81(6):2564-72
pubmed: 17182683
Lancet. 2012 Jan 14;379(9811):153-64
pubmed: 21855993
BMC Vet Res. 2015 Aug 14;11:205
pubmed: 26272639
Bioorg Med Chem. 2015 Feb 1;23(3):466-70
pubmed: 25564380
Crit Rev Food Sci Nutr. 2006;46(2):185-96
pubmed: 16431409
J Cancer Prev. 2020 Dec 30;25(4):244-251
pubmed: 33409257
Anal Bioanal Chem. 2013 Aug;405(20):6563-72
pubmed: 23748498
J Agric Food Chem. 2002 May 22;50(11):3228-31
pubmed: 12009991
Nat Prod Commun. 2014 Jan;9(1):51-4
pubmed: 24660461
Molecules. 2018 Aug 17;23(8):
pubmed: 30126139
Curr Opin Immunol. 2012 Aug;24(4):507-11
pubmed: 22541724
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011 Sep;112(3):e31-5
pubmed: 21827957
Hepatology. 2020 Feb;71(2):686-721
pubmed: 31816111
Sci Rep. 2016 Jun 03;6:27156
pubmed: 27257160
Pediatr Rev. 2009 Apr;30(4):119-29; quiz 130
pubmed: 19339385
Biochem Biophys Res Commun. 2000 Sep 24;276(2):534-8
pubmed: 11027509
Nat Struct Mol Biol. 2011 Feb;18(2):135-41
pubmed: 21217702
Viruses. 2019 Jul 07;11(7):
pubmed: 31284698
Int J Cancer. 2000 Dec 15;88(6):1003-8
pubmed: 11093828
J Virol. 2011 May;85(9):4386-98
pubmed: 21307190
J Hepatol. 2013 May;58(5):861-7
pubmed: 23246506
BMC Complement Altern Med. 2011 Feb 25;11:16
pubmed: 21352539

Auteurs

Rinu Sivarajan (R)

Institute for Virology and Immunobiology, Julius-Maximilians-University of Würzburg, Versbacher Strasse 7, 97078, Würzburg, Germany.
Chair of Tissue Engineering and Regenerative Medicine, University Hospital Würzburg, Würzburg, Germany.

Heike Oberwinkler (H)

Chair of Tissue Engineering and Regenerative Medicine, University Hospital Würzburg, Würzburg, Germany.

Valeria Roll (V)

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

Eva-Maria König (EM)

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

Maria Steinke (M)

Chair of Tissue Engineering and Regenerative Medicine, University Hospital Würzburg, Würzburg, Germany.
Fraunhofer Institute for Silicate Research ISC, Röntgenring 11, 97070, Würzburg, Germany.

Jochen Bodem (J)

Institute for Virology and Immunobiology, Julius-Maximilians-University of Würzburg, Versbacher Strasse 7, 97078, Würzburg, Germany. Jochen.Bodem@uni-wuerzburg.de.

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