Lithocholic acid exerts antiviral activity against porcine epidemic diarrhea virus by enhancing TGR5-mediated type III interferon production.

Lithocholic acid exerts antiviral activity against porcine epidemic diarrhea virus by enhancing TGR5-mediated type III interferon production.

Publication date: Jan 01, 2026

Porcine epidemic diarrhea virus (PEDV), a highly infectious porcine virus, leads to high mortality in newborn piglets. Bile acids (BAs) are synthesized in the liver and metabolized in the intestines by gut microbiota. These acids can regulate cellular immunity and influence viral infection processes. To assess the antiviral activity of four BAs-cholic acid (CA), chenodeoxycholic acid (CDCA), deoxycholic acid (DCA), and lithocholic acid (LCA) against PEDV in IPEC-J2 cells. We investigated the effects of 24-h pretreatment with the four aforementioned BAs at varying concentrations on PEDV replication in IPEC-J2 cells through quantitative polymerase chain reaction (qPCR), Western blotting, and TCID assay. BA exposure inhibited PEDV N protein expression to varying degrees. qPCR and Western blotting to measure PEDV N protein and mRNA expression at varying LCA concentrations (1, 5, or 10 μM) revealed that LCA demonstrated significant anti-PEDV activity in a concentration-dependent manner (p

Concepts Keywords
10m Animals
Chenodeoxycholic Antiviral Agents
Liver Antiviral Agents
Piglets Cell Line
Virus Chenodeoxycholic Acid
Chenodeoxycholic Acid
Coronavirus Infections
IFN-λ
Interferons
Interferons
Lithocholic Acid
Lithocholic Acid
Lithocholic acid
PEDV
Receptors, G-Protein-Coupled
Receptors, G-Protein-Coupled
Swine
Swine Diseases
Virus Replication

Semantics

Type Source Name
disease MESH diarrhea
disease MESH viral infection
drug DRUGBANK Cholic Acid
drug DRUGBANK Chenodeoxycholic acid
drug DRUGBANK Deoxycholic Acid
drug DRUGBANK Dichloroacetic Acid
disease MESH LCA
disease MESH Coronavirus Infections
disease MESH Swine Diseases

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