# Rhus coriaria Linn Extract as a Natural Inhibitor of Influenza A Virus Replication In Vitro

**Authors:** Carla Prezioso, Maria Luisa Savo Sardaro, Flavio Frezza, Dolores Limongi, Salvatore Velotto, Leonardo Lupacchini, Giovanni D’Auria, Marta De Angelis, Lucia Nencioni, Paola Checconi

PMC · DOI: 10.3390/cimb48020207 · 2026-02-13

## TL;DR

This study shows that an extract from Rhus coriaria L. can inhibit the replication of Influenza A virus in human bronchial cells.

## Contribution

The novel contribution is the experimental evidence that Rhus coriaria extract reduces influenza A virus replication in vitro.

## Key findings

- Rhus coriaria extract significantly reduced viral load in a dose-dependent manner.
- The extract decreased mRNA and protein levels of key influenza A virus components like HA, NA, and M2.
- Multiple methods confirmed reduced viral replication at both transcriptional and protein levels.

## Abstract

Influenza A viruses remain a major public health threat due to their high mutation rates, antigenic variability, and the emergence of resistance to current antivirals, underscoring the need for novel therapeutic options. Natural compounds rich in polyphenols and flavonoids have attracted increasing attention as potential broad-spectrum antiviral agents. In this study, the activity of Rhus coriaria L. water extract against Influenza A virus in BEAS-2B human bronchial epithelial cells was investigated. Cell viability assay identified non-cytotoxic concentrations, up to 0.1 mg/mL, which were used in infection experiments. Viral replication was assessed at multiple levels by quantitative real-time PCR, western blotting, immunofluorescence and tissue culture infectious dose 50% (TCID50). Treatment with R. coriaria extract resulted in a dose-dependent and statistically significant reduction of viral load. The extract decreased mRNA levels of Hemagglutin (HA), Neuraminidase (NA) and Matrix protein 2 (M2). Consistently, western blot analysis showed a decrease in major viral proteins HA, Nucleoprotein (NP), Matrix protein 1 (M1) and Polymerase Acidic protein (PA). Confocal images revealed a marked reduction in HA and PA signals, results that are statistically significant according to quantitative fluorescence evaluation. The convergence of results obtained through independent methodologies at both the transcriptional and protein levels highlight the robustness of the findings. These data provide the experimental evidence that Rhus coriaria interferes with influenza A virus replication in airway epithelial cells and support its further investigation as a promising phytochemical platform for the development of novel anti-influenza strategies.

## Linked entities

- **Genes:** ha (hair bristles) [NCBI Gene 251217], XK (X-linked Kx blood group antigen, Kell and VPS13A binding protein) [NCBI Gene 7504], M2 (matrix protein 2) [NCBI Gene 956528], PNP (purine nucleoside phosphorylase) [NCBI Gene 4860], CHRM1 (cholinergic receptor muscarinic 1) [NCBI Gene 1128], AMY2A (amylase alpha 2A) [NCBI Gene 279]

## Full-text entities

- **Genes:** NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, M2 (matrix protein 2) [NCBI Gene 956528], KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, NEU1 (neuraminidase 1) [NCBI Gene 4758] {aka NANH, NEU, SIAL1}
- **Diseases:** Cytotoxicity (MESH:D064420), infected (MESH:D007239), COVID-19 (MESH:D000086382), Virus Infection (MESH:D014777), Influenza (MESH:D007251), injury to (MESH:D014947), inflammatory (MESH:D007249), respiratory (MESH:D012131)
- **Chemicals:** tannins (MESH:D013634), delphinidin (MESH:C017185), MTT (MESH:C070243), penicillin (MESH:D010406), A120-101P (-), flavonoid (MESH:D005419), 4'6-diamidino-2-phenylindole (MESH:C007293), Alexa Fluor 546 (MESH:C481052), Anthocyanins (MESH:D000872), protocatechuic acid (MESH:C009091), Polyphenols (MESH:D059808), glutamine (MESH:D005973), Acetonitrile (MESH:C032159), Triton X-100 (MESH:D017830), streptomycin (MESH:D013307), quercetin (MESH:D011794), formic acid (MESH:C030544), Oxygen (MESH:D010100), gallotannin (MESH:C000726650), Gallic acid (MESH:D005707), biflavonoids (MESH:D044946), metal (MESH:D008670), chalcones (MESH:D047188), methanol (MESH:D000432), acrylamide (MESH:D020106), malic acid (MESH:C030298), B (MESH:D001895), DTT (MESH:D004229), SDS (MESH:D012967), Myricetin (MESH:C040015), phenolic acid (MESH:C017616), TRIzol (MESH:C411644), catechins (MESH:D002392), water (MESH:D014867), gallotannins (MESH:D047348), kaempferol (MESH:C006552)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721], Orthomyxoviridae (family) [taxon 11308], Alphainfluenzavirus (genus) [taxon 197911], Influenza A virus (no rank) [taxon 11320], Mus musculus (house mouse, species) [taxon 10090], Caenorhabditis elegans (species) [taxon 6239], Rhus (genus) [taxon 4012], Rhus coriaria (Sicilian sumac, species) [taxon 298661], Toxicodendron succedaneum (wax tree, species) [taxon 269721], H1N1 subtype (serotype) [taxon 114727], Human immunodeficiency virus 1 (no rank) [taxon 11676], Hepatitis B virus (no rank) [taxon 10407], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]
- **Cell lines:** MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422), PA5-32223 — Gallus gallus (Chicken), Marek disease, Cancer cell line (CVCL_T629), BEAS-2B — Homo sapiens (Human), Transformed cell line (CVCL_0168)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939942/full.md

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Source: https://tomesphere.com/paper/PMC12939942