# One Health Investigation of Stage-Dependent Antimicrobial Resistance Patterns Across Intermediate and Ripened Dairy Matrices: The Tyrovolia–Kopanisti Paradigm

**Authors:** Georgios Rozos, Konstantina Fotou, Vaia Gerokomou, Konstantina Nikolaou, Aikaterini Dadamogia, Lampros Hatzizisis, Ioannis Skoufos, Athina Tzora, Eugenia Bezirtzoglou, Chrysoula (Chrysa) Voidarou

PMC · DOI: 10.3390/microorganisms14030712 · Microorganisms · 2026-03-22

## TL;DR

This study shows that artisanal dairy fermentation can track changes in antibiotic resistance over time, acting as a natural indicator of local resistance trends.

## Contribution

The study introduces artisanal dairy fermentation as a One Health model for monitoring stage-dependent antimicrobial resistance patterns.

## Key findings

- Resistance increased significantly from 69.88% at day 5 to 77.25% at day 30 of fermentation.
- Multidrug resistance rose from 37.57% to 60.73% of resistant isolates during fermentation.
- Resistance to metronidazole, chloramphenicol, and others increased significantly, while erythromycin and oxytetracycline resistance declined.

## Abstract

Antimicrobial resistance (AMR) emerges and circulates across interconnected human, animal, food, and environmental reservoirs; however, food fermentation systems remain underexplored as indicators of local AMR pressure, even though artisanal dairy fermentations may function as natural sentinels of AMR. In this study, we used an artisanal dairy fermentation chain as a One Health model to investigate whether environmentally exposed lactobacilli can reflect stage-associated shifts in resistance. A total of 1.085 isolates representing 16 Lactobacillus species were recovered from the same artisanal dairy matrix at two fermentation stages: day 5 (“Tyrovolia”; n = 518) and day 30 (“Kopanisti”; n = 567). Susceptibility to 14 antibiotics was evaluated by broth micro-dilution, and L. acidophilus was further screened for selected resistance genes. Overall resistance increased significantly from 69.88% (362/518) at day 5 to 77.25% (438/567) at day 30 (p = 0.0059), while multidrug resistance rose from 37.57% to 60.73% of resistant isolates (p < 0.001). Across the 224 species–antibiotic combinations examined, 129 (57.58%) showed an increased upper MIC limit at day 30, and resistance increased significantly for 9 of the 14 antibiotics tested, with the largest rises observed for metronidazole (RR = 7.67), chloramphenicol (RR = 5.74), quinupristin/dalfopristin (RR = 4.11), vancomycin (RR = 2.78), and trimethoprim (RR = 2.43). In contrast, erythromycin and oxytetracycline resistance declined significantly at the ripened stage. In L. acidophilus, 21 resistance genes were detected in 14/70 day-5 isolates and 19 genes in 13/71 day-30 isolates, but marked genotype–phenotype discordance was observed, including matrix-dependent expression patterns for tetM, ermB, and blaTEM. Collectively, these findings show that environmentally exposed artisanal dairy fermentations can enrich resistance phenotypes and may serve as sensitive sentinels of AMR dynamics at the human–animal–environment interface.

## Linked entities

- **Genes:** tet(M) (tetracycline resistance ribosomal protection protein Tet(M)) [NCBI Gene 8154447], erm(B) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(B)) [NCBI Gene 8154416]
- **Chemicals:** metronidazole (PubChem CID 4173), chloramphenicol (PubChem CID 5959), quinupristin/dalfopristin (PubChem CID 11979418), vancomycin (PubChem CID 14969), trimethoprim (PubChem CID 5578), erythromycin (PubChem CID 12560), oxytetracycline (PubChem CID 54675779)
- **Species:** Lactobacillus (taxon 1578)

## Full-text entities

- **Chemicals:** vancomycin (MESH:D014640), quinupristin/dalfopristin (MESH:C062940), metronidazole (MESH:D008795), erythromycin (MESH:D004917), chloramphenicol (MESH:D002701), oxytetracycline (MESH:D010118), trimethoprim (MESH:D014295)
- **Species:** Lactobacillus acidophilus (species) [taxon 1579], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

112 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028824/full.md

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Source: https://tomesphere.com/paper/PMC13028824