The Novel A-Type Proanthocyanidin-Rich Phytocomplex SP4™ Acts as a Broad-Spectrum Antiviral Agent against Human Respiratory Viruses.
Proanthocyanidins
/ pharmacology
Antiviral Agents
/ pharmacology
Humans
SARS-CoV-2
/ drug effects
Virus Replication
/ drug effects
Coronavirus OC43, Human
/ drug effects
Animals
Dogs
Influenza A virus
/ drug effects
Coronavirus 229E, Human
/ drug effects
Spike Glycoprotein, Coronavirus
/ metabolism
Chlorocebus aethiops
A-type proanthocyanidins
SP4™ phytocomplex
broad-spectrum antiviral activity
coronaviruses
influenza virus
natural antivirals
respiratory syncytial virus
virucidal activity
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
05 Jul 2024
05 Jul 2024
Historique:
received:
27
05
2024
revised:
01
07
2024
accepted:
03
07
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
The appearance of new respiratory virus infections in humans with epidemic or pandemic potential has underscored the urgent need for effective broad-spectrum antivirals (BSAs). Bioactive compounds derived from plants may provide a natural source of new BSA candidates. Here, we investigated the novel phytocomplex formulation SP4™ as a candidate direct-acting BSA against major current human respiratory viruses, including coronaviruses and influenza viruses. SP4™ inhibited the in vitro replication of SARS-CoV-2, hCoV-OC43, hCoV-229E, Influenza A and B viruses, and respiratory syncytial virus in the low-microgram range. Using hCoV-OC43 as a representative respiratory virus, most of the antiviral activity of SP4™ was observed to stem primarily from its dimeric A-type proanthocyanidin (PAC-A) component. Further investigations of the mechanistic mode of action showed SP4™ and its PAC-A-rich fraction to prevent hCoV-OC43 from attaching to target cells and exert virucidal activity. This occurred through their interaction with the spike protein of hCoV-OC43 and SARS-CoV-2, thereby interfering with spike functions and leading to the loss of virion infectivity. Overall, these findings support the further development of SP4™ as a candidate BSA of a natural origin for the prevention of human respiratory virus infections.
Identifiants
pubmed: 39000477
pii: ijms25137370
doi: 10.3390/ijms25137370
pii:
doi:
Substances chimiques
Proanthocyanidins
0
Antiviral Agents
0
proanthocyanidin
18206-61-6
Spike Glycoprotein, Coronavirus
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : EU funding within the MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases
ID : PE00000007, INF-ACT
Organisme : Piedmont Region
ID : PAR FSC INFRA-P2 B COVID
Organisme : University of Turin
ID : Ricerca Locale