Hydroxychloroquine inhibits porcine epidemic diarrhea virus infection by targeting post-attachment stages and virus-induced inflammation in vitro.

Publication date: Aug 01, 2026

Porcine epidemic diarrhea virus (PEDV) causes severe enteric disease in swine and represents a substantial economic threat to the global swine industry. Although vaccines are available, effective antiviral strategies against PEDV remain limited. Hydroxychloroquine (HCQ) is a lysosomotropic agent with reported antiviral and immunomodulatory properties; however, its effects on PEDV infection have not been fully elucidated. In this study, we evaluated the antiviral activity of HCQ against PEDV in vitro and examined its effects on distinct stages of the viral life cycle and host inflammatory signaling. HCQ significantly reduced PEDV replication, viral protein expression, and infectious virus production, as demonstrated by RT-qPCR, Western blotting, immunofluorescence analysis, and plaque assays. Time-of-addition experiments revealed that HCQ exerted minimal effects on virus attachment but effectively inhibited viral internalization, replication, and release. Moreover, HCQ markedly suppressed PEDV-induced expression of pro-inflammatory cytokines, including IL-1β, IL-6, IL-8, and TNF-α, and attenuated activation of the nuclear factor kappa B (NF-_705B) signaling pathway. Collectively, these findings demonstrate that HCQ exerts dual antiviral and anti-inflammatory effects against PEDV infection in vitro, highlighting its potential as a host-targeted antiviral strategy.

Concepts Keywords
Diarrhea Animals
Hydroxychloroquine Anti-Inflammatory Agents
Immunofluorescence Anti-Inflammatory Agents
Nuclear Antiviral Agents
Pro Antiviral Agents
Cell Line
Chlorocebus aethiops
Coronavirus Infections
Cytokines
Cytokines
Hydroxychloroquine
Hydroxychloroquine
Hydroxychloroquine (HCQ)
Inflammation
Interleukin-6
Interleukin-6
NF-kappa B
NF-kappa B
Pro-inflammatory cytokines
Signal Transduction
Swine
Swine Diseases
Tumor Necrosis Factor-alpha
Tumor Necrosis Factor-alpha
Vero Cells
Virus Attachment
Virus Internalization
Virus Replication

Semantics

Type Source Name
drug DRUGBANK Hydroxychloroquine
disease MESH diarrhea
disease MESH virus infection
disease MESH inflammation
disease MESH infection
pathway KEGG Viral life cycle
pathway REACTOME Release
disease MESH Coronavirus Infections
pathway REACTOME Signal Transduction
disease MESH Swine Diseases

Original Article

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