Anti-Herpetic Activity of Killer Peptide (KP): An In Vitro Study.
Antiviral Agents
/ pharmacology
Herpesvirus 1, Human
/ drug effects
Herpesvirus 2, Human
/ drug effects
Chlorocebus aethiops
Vero Cells
Animals
Acyclovir
/ pharmacology
Humans
Virus Replication
/ drug effects
Drug Resistance, Viral
/ drug effects
Herpes Simplex
/ drug therapy
Antimicrobial Peptides
/ pharmacology
HSV-1
HSV-2
Killer Peptide (KP)
antimicrobial peptides
antivirals
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:
01 Oct 2024
01 Oct 2024
Historique:
received:
16
09
2024
revised:
27
09
2024
accepted:
30
09
2024
medline:
16
10
2024
pubmed:
16
10
2024
entrez:
16
10
2024
Statut:
epublish
Résumé
Antimicrobial peptides represent a promising alternative to traditional drugs in relation to cost, toxicity, and, primarily, the growing problem of drug resistance. Here, we report on the activity against HSV-1 and HSV-2 of a previously described wide-spectrum synthetic decapeptide, Killer Peptide (KP). As determined by plaque reduction assays, treatment with KP at 100 μg/mL resulted in a reduction in the viral yield titer of 3.5 Logs for HSV-1 and 4.1 Logs for HSV-2. Further evaluation of KP antiviral activity focused on the early stages of the virus replicative cycle, including the determination of the residual infectivity of viral suspensions treated with KP. A direct effect of the peptide on viral particles impairing virus absorption and penetration was shown. The toxicity profile proved to be extremely good, with a selectivity index of 29.6 for HSV-1 and 156 for HSV-2. KP was also active against acyclovir (ACV)-resistant HSV isolates, while HSV subcultures in the presence of sub-inhibitory doses of KP did not lead to the emergence of resistant strains. Finally, the antiviral action of KP proved to be synergistic with that of ACV. Overall, these results demonstrate that KP could represent an interesting addition/alternative to acyclovir for antiviral treatment.
Identifiants
pubmed: 39408931
pii: ijms251910602
doi: 10.3390/ijms251910602
pii:
doi:
Substances chimiques
Antiviral Agents
0
Acyclovir
X4HES1O11F
Antimicrobial Peptides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministero dell'Università e della Ricerca
ID : D.M. 737/2021 - PNR - PNRR - NextGenerationEU and local funding