# Decoding the antiviral potential of eugenol, thymol and vanillin against human cytomegalovirus infection

**Authors:** Clara Martín-Martín, María Ruiz-Rico, José Manuel Barat, Estéfani García-Ríos, Pilar Pérez-Romero

PMC · DOI: 10.1099/jgv.0.002248 · 2026-03-18

## TL;DR

This study explores how eugenol, thymol, and vanillin can fight human cytomegalovirus in different cell types, showing promise as alternative or complementary treatments.

## Contribution

The study identifies the antiviral mechanisms and synergistic effects of essential oil components against HCMV in different cell lines.

## Key findings

- Vanillin showed the highest antiviral efficacy with low toxicity and high selectivity in both epithelial and fibroblast cells.
- Eugenol and thymol exhibited distinct mechanisms in different cell lines, including virucidal activity and inhibition of viral entry and gene expression.
- Combining essential oil components with ganciclovir produced synergistic effects, enhancing antiviral outcomes in specific cell types.

## Abstract

Human cytomegalovirus (HCMV) poses serious health risks, particularly for immunocompromised individuals. However, the current FDA-approved anti-HCMV drugs face challenges such as drug resistance and significant side effects, underscoring the need for alternative treatment options. Essential oil components (EOCs), including eugenol, thymol and vanillin, are recognized for their therapeutic potential. This study evaluates their antiviral effects against HCMV in epithelial (ARPE-19) and fibroblast (MRC-5) cell lines. Among the EOCs, vanillin demonstrated the highest efficacy, characterized by low toxicity and a high selectivity index in both cell types. Mechanistic differences were noted between the cell lines. In ARPE-19 cells, eugenol showed virucidal activity, inhibited viral entry and suppressed early gene expression (IE-1). Conversely, in MRC-5 cells, eugenol mainly blocked viral entry and exhibited virucidal effects. Thymol was most effective in ARPE-19 cells, where it completely suppressed IE-1 expression as a result of both inhibition of viral entry and a direct disruptive effect on IE-1 expression. In addition, thymol showed an effect on viral replication. In MRC-5 cells, thymol primarily inhibited viral entry and attachment. Vanillin exhibited dual inhibitory activity in both cell lines, blocking viral attachment and entry. In MRC-5, vanillin also appears to affect intermediate processes. Notably, combining EOCs with ganciclovir resulted in synergistic effects. The eugenol/ganciclovir combination was particularly effective in ARPE-19 cells, while thymol/ganciclovir showed enhanced efficacy in MRC-5 cells. These findings suggest that EOCs have significant potential as adjunct therapies to improve antiviral outcomes and address drug-resistant HCMV strains.

## Linked entities

- **Genes:** ie1 (IE1) [NCBI Gene 921845]
- **Chemicals:** eugenol (PubChem CID 3314), thymol (PubChem CID 6989), vanillin (PubChem CID 1183), ganciclovir (PubChem CID 135398740)

## Full-text entities

- **Genes:** GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}
- **Diseases:** HIV-infected (MESH:D015658), respiratory tract infections (MESH:D012141), EOCs (MESH:C566443), congenital infections (MESH:D007239), viral diseases (MESH:D014777), disorders of (MESH:D009358), motor disabilities (MESH:D009069), burns (MESH:D002056), mental retardation (MESH:D008607), cytotoxic (MESH:D064420), system (MESH:D015619), HCMV infection (MESH:D003586), birth defects (MESH:D000014), inflammatory (MESH:D007249), hearing loss (MESH:D034381), , cardiovascular and nervous systems (MESH:D018376)
- **Chemicals:** Flavopiridol (MESH:C077990), 1X PFA (-), carvacrol (MESH:C073316), streptomycin (MESH:D013307), vanillic acid (MESH:D014641), citrate (MESH:D019343), PBS (MESH:D007854), glutamine (MESH:D005973), GCV (MESH:D015774), DMSO (MESH:D004121), penicillin (MESH:D010406), 4-hydroxy-3-methoxybenzaldehyde (MESH:C100058), Tween 20 (MESH:D011136), CO2 (MESH:D002245), SDS (MESH:D012967), PFA (MESH:C003043), heparin (MESH:D006493), TH (MESH:D013943), EU (MESH:D005054), EO (MESH:D009822)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Rattus norvegicus (brown rat, species) [taxon 10116], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298], Adenoviridae (family) [taxon 10508], Human immunodeficiency virus 1 (no rank) [taxon 11676], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Thymus vulgaris (common thyme, species) [taxon 49992], Homo sapiens (human, species) [taxon 9606], Human betaherpesvirus 5 (no rank) [taxon 10359], Syzygium aromaticum (clove, species) [taxon 219868], Coxsackievirus (species) [taxon 12066], Enterovirus (genus) [taxon 12059]
- **Cell lines:** MRC-5 — Homo sapiens (Human), Finite cell line (CVCL_0440), ARPE- — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0145), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12999277/full.md

---
Source: https://tomesphere.com/paper/PMC12999277