Gold/Silver Hybrid Nanoparticles with Enduring Inhibition of Coronavirus Multiplication through Multisite Mechanisms.
Ting DuJinyu ZhangChunqiao LiTao SongPing LiJifeng LiuXin-Jun DuShuo WangPublished in: Bioconjugate chemistry (2020)
As a large enveloped RNA virus, coronavirus is of considerable medical and veterinary significance, and anticoronavirus treatment is challenging due to its biodiversity and rapid variability. In this study, Au@Ag nanorods (Au@AgNRs) were successfully synthesized by coating AuNRs with silver and were shown for the first time to have activity against the replication of porcine epidemic diarrhea virus (PEDV). Viral titer analysis demonstrated that Au@AgNRs could inhibit PEDV infection by 4 orders of magnitude at 12 h post-infection, which was verified by viral protein expression analysis. The potential mechanism of action showed that Au@AgNRs could inhibit the entry of PEDV and decrease the mitochondrial membrane potential and caspase-3 activity. Additionally, we demonstrated that a large amount of virus proliferation can cause the generation of reactive oxygen species in cells, and the released Ag+ and exposed AuNRs by Au@AgNRs after the stimulation of reactive oxygen species has superior antiviral activity to ensure long-term inhibition of the PEDV replication cycle. The integrated results support that Au@AgNRs can serve as a potential therapeutic strategy to prevent the replication of coronavirus.
Keyphrases
- sensitive detection
- reduced graphene oxide
- sars cov
- reactive oxygen species
- gold nanoparticles
- visible light
- quantum dots
- induced apoptosis
- signaling pathway
- oxidative stress
- silver nanoparticles
- respiratory syndrome coronavirus
- cell cycle arrest
- amino acid
- coronavirus disease
- small molecule
- irritable bowel syndrome