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Antiviral activity of phage display-selected peptides against Japanese encephalitis virus infection in vitro and in vivo
- Source :
- Antiviral research. 174
- Publication Year :
- 2019
-
Abstract
- Japanese Encephalitis virus (JEV) is a zoonotic flavivirus that is the most significant etiological agent of childhood viral neurological infections. However, no specific antiviral drug is currently available to treat JEV infections. The JEV envelope (E) protein is a class II viral fusion protein that mediates host cell entry, making interference with the interaction between the E protein of JEV and its cognate receptors an attractive strategy for anti-JEV drug development. In this study, we identified a peptide derived from a phage display peptide library against the E protein of JEV, designated P1, that potentially inhibits in vitro and in vivo JEV infections. P1 inhibits JEV infection in BHK-21 cells with 50% inhibitory capacity at a concentration of 35.9 μM. The time-of-addition assay indicates that JEV replication is significantly inhibited during pre-infection and co-infection of P1 with JEV while post-infection treatments with P1 have very little impact on JEV proliferation, showing that P1 inhibits JEV infection at early stages and indicating the potential prophylactic effect of P1. We adapted an in vitro BiFC assay system and demonstrated that P1 interacts with JEV E proteins and blocks their entry into cells. We also evaluated the therapeutic efficacy of P1 in a lethal JEV mouse model exhibiting systemic and brain infections. Interestingly, P1 treatment protected C57BL/6 mice against mortality, markedly reduced the viral loads in blood and brain, and diminished the histopathological lesions in the brain cells. In addition to controlling systemic infection, P1 has a very low level of cytotoxicity and acts in a sequence-specific manner, as scrambled peptide sP1 does not show any antiviral activity. In conclusion, our in vitro and in vivo experimental findings show that P1 possesses antiviral activity against JEV infections, is safe to use, and has potential for further development as an antiviral treatment against JEV infections.
- Subjects :
- 0301 basic medicine
Phage display
medicine.drug_class
viruses
030106 microbiology
Virus Attachment
Virus Replication
Antiviral Agents
Virus
Cell Line
03 medical and health sciences
Mice
Viral Envelope Proteins
In vivo
Peptide Library
Virology
medicine
Animals
Encephalitis, Japanese
Pharmacology
Encephalitis Virus, Japanese
biology
Japanese encephalitis
Viral Load
medicine.disease
biology.organism_classification
In vitro
Mice, Inbred C57BL
Flavivirus
Disease Models, Animal
030104 developmental biology
Female
Antiviral drug
Viral load
Subjects
Details
- ISSN :
- 18729096
- Volume :
- 174
- Database :
- OpenAIRE
- Journal :
- Antiviral research
- Accession number :
- edsair.doi.dedup.....484e993743baf9d06e10628b93ca345b