# Seasonal prevalence of extended-spectrum β-lactamase–producing bacteria in food-chain animals, humans, and the surrounding environment in Fayoum governorate: a one health approach

**Authors:** Ayatollah S. El-Zayat, Shrouk E. Khalil, Marwa N. Ahmed, Dina El-Sayed, Neveen Rabie, Enas A. H. Farag, Hanan A. Goda, Ahmad F. Al-Shahaby, Hala R. Ali

PMC · DOI: 10.3389/fmicb.2026.1726798 · Frontiers in Microbiology · 2026-02-04

## TL;DR

This study shows how the presence of drug-resistant bacteria varies with seasons in animals, humans, and environments in Egypt, highlighting the need for One Health surveillance.

## Contribution

This is the first comprehensive investigation of seasonal ESBL prevalence in animals, humans, and environments across three seasons in Egypt.

## Key findings

- ESBL-producing E. coli prevalence was highest in summer and fall, while K. pneumoniae peaked in winter.
- Environmental samples showed fluctuating ESBL trends, indicating farm environments' role in persistence and spread.
- Genotypic resistance genes like blaSHV and blaCTX-M1 correlated with phenotypic resistance and multidrug resistance patterns.

## Abstract

Extended-spectrum β-lactamase (ESBL) producers, particularly Escherichia coli and Klebsiella pneumoniae, pose a growing One Health challenge influenced by seasonal variation. This study assessed seasonal impacts on ESBL prevalence among humans, animals, and farm environments. A total of 2,890 poultry samples, 864 samples from dairy cows (including 88 milk samples and 776 rectal swabs), 248 human fecal samples (118 farm workers and 130 hospitalized patients) and 583 environmental samples were collected from Fayoum governorate, across three seasons. The isolation data revealed significant seasonal impacts, particularly in dairy cows and environmental samples, with source-related differences evident within the same season. The phenotypic and genotypic ESBL- analysis of all isolates from different sources across seasons showed that ESBL-producing E. coli demonstrated comparable prevalence in summer (14.68%) and fall (15%) before declining in winter (7.5%), while K. pneumoniae showed the highest prevalence in winter (29.4%), with lower detection in summer (11.9%) and absence in fall. Significant seasonal differences were detected, with ESBL-producing E. coli prevalence varying across sources in the fall (p = 0.039) and ESBL-producing K. pneumoniae showing variation in poultry across seasons (p = 0.042). Environmental isolates exhibited fluctuating trends, highlighting the role of farm environments in ESBL persistence and dissemination. At the genetic level, blaSHV and blaCTX-M1 demonstrated seasonal variation, whereas blaTEM showed no variation. Heat-map and hierarchical clustering showed significant correlation among harboring ESBL-genes, particularly blaSHV and blaCTX-M1, and resistance profiles to β-lactams antibiotics, as well as to non-beta-lactam antibiotics. Additionally, source- and species-based seasonal effects were observed in the prevalence of E. coli, K. pneumoniae, and their associated ESBL traits. The results further demonstrated that genotypic resistance determinants (bla genes) are significantly linked to phenotypic resistance, especially to β-lactams, and also reflected multi-drug resistance patterns that indicate co-selection across unrelated antibiotic classes. These findings highlight the public health significance of ESBL-producing E. coli and K. pneumoniae, both as pathogens and as disseminators of multidrug resistance determinants, emphasizing the need for One Health surveillance. To the best of our knowledge, this is the first systematic and comprehensive investigation of ESBL prevalence across animal, human and environmental, over three distinct seasons.

## Linked entities

- **Genes:** bla SHV (class A extended-spectrum beta-lactamase SHV-2) [NCBI Gene 40101717]
- **Species:** Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** blaTEM [NCBI Gene 13905334], ESBL [NCBI Gene 13906541], sul1 [NCBI Gene 7872757], AmpC [NCBI Gene 7872529]
- **Diseases:** zoonotic disease (MESH:D015047), DDST (MESH:D013736), Double disc synergy (MESH:D005671), mastitis (MESH:D008413), infections (MESH:D007239)
- **Chemicals:** SXT (MESH:D015662), Cefepime (MESH:D000077723), methyl red (MESH:C008492), MEM (MESH:D000077731), carbapenem (MESH:D015780), CAZ (MESH:D002442), citrate (MESH:D019343), AM (MESH:D000667), water (MESH:D014867), oxytetracycline (MESH:D010118), indole (MESH:C030374), chloramphenicol (MESH:D002701), STX (MESH:D012530), beta-lactam (MESH:D047090), ATM (MESH:C020809), penicillin (MESH:D010406), aztreonam (MESH:D001398), Cefotaxime (MESH:D002439), NaCl (MESH:D012965), CTX (-), TE (MESH:D013691), monobactam (MESH:D008997), C (MESH:D002244), CIP (MESH:D002939), quinolones (MESH:D015363), Ceftriaxone (MESH:D002443), AMC (MESH:D019980), sulfonamides (MESH:D013449), cephalosporin (MESH:D002511)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Enterobacteriaceae (enterobacteria, family) [taxon 543], Sus scrofa (pig, species) [taxon 9823], Salmonella (genus) [taxon 590], Escherichia coli (E. coli, species) [taxon 562], Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913390/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913390/full.md

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Source: https://tomesphere.com/paper/PMC12913390