# A One Health assessment of antimicrobial-resistant Enterobacterales in migratory little stints (Calidris minuta) and aquatic ecosystems in the Kenyan Rift Valley

**Authors:** Catherine W. Mbuthia, Rael J. Too, Alexanda Mzula, Titus S. Imboma, John Kiiru, Samuel Kariuki, Abubakar S. Hoza, Mabel Kamweli Aworh, Mabel Kamweli Aworh, Mabel Aworh

PMC · DOI: 10.1371/journal.pone.0336315 · PLOS One · 2026-03-27

## TL;DR

This study shows that migratory little stints in Kenya carry antibiotic-resistant bacteria, highlighting their role in spreading antimicrobial resistance across regions.

## Contribution

The study is the first to link little stints to the antimicrobial resistance epidemiological circuit.

## Key findings

- Enterobacter spp and Escherichia coli were the most common resistant bacteria found in bird and water samples.
- Multidrug-resistant and ESBL-producing Enterobacterales were detected regardless of human activity levels in the environment.
- Resistant strains were found to be widespread, suggesting a need for expanded AMR surveillance including migratory birds.

## Abstract

Palearctic migratory little stints (Calidris minuta) can acquire resistant bacteria from contaminated environments and facilitate their transboundary spread. This two-year repeated cross-sectional study assessed the frequency and distribution of multidrug-resistant (MDR) and extended-spectrum beta-lactamase (ESBL)-producing Enterobacterales. Isolates were recovered from fecal samples of C. minuta foraging at the shores of Lakes Bogoria (low anthropogenic activities) and Magadi (high anthropogenic activities), as well as from peripheral freshwater sources shared by birds, humans, livestock and wildlife. A total of 184 fecal samples and 48 water samples were collected upon the birds’ arrival from the Arctic (cohort 1) and pre-departure from the Rift Valley lakes (cohort 2). Samples were cultured, bacterial isolates were identified using MALDI-TOF MS platform and tested against 12 antimicrobials using the Kirby-Bauer disk method. Of the 294 isolates (16 genera and 33 species), Enterobacter spp (31.0%, n = 91) and Escherichia coli (17.3%, n = 51) predominated. Resistance was highest for ampicillin (50%) and lowest for meropenem (1.0%). The predominant MDR phenotype was a combination of resistances to ampicillin, tetracycline, and sulfamethoxazole-trimethoprim. Specifically, 38 (12.9%) isolates were MDR, 37 (12.6%) co-expressed ESBL-MDR traits, and 19 (6.5%) were ESBL producers that did not meet MDR criteria. Enterobacter spp showed the highest frequencies of MDR (8.2%, n = 24) and combined ESBL-MDR (4.8%, n = 14) phenotypes, while Acinetobacter spp (3.4%, n = 10) were the most frequent ESBL producers. The statistically non-significant differences (p > 0.05) across study areas, sample sources, and cohorts suggest that resistant strains are pervasive throughout these landscapes, irrespective of anthropogenic pressures. This is the first study to link C. minuta to the antimicrobial resistance (AMR) epidemiological circuit. Our findings underscore the need to include migratory wild birds in AMR surveillance and utilizing whole-genome sequencing to accurately trace the origin and dissemination pathways of AMR strains.

## Linked entities

- **Chemicals:** ampicillin (PubChem CID 6249), tetracycline (PubChem CID 54675776), sulfamethoxazole-trimethoprim (PubChem CID 358641), meropenem (PubChem CID 441130)
- **Species:** Calidris minuta (taxon 670340), Escherichia coli (taxon 562), Acinetobacter sp. P (taxon 596119)

## Full-text entities

- **Diseases:** AMR (MESH:D060467), ESBL (MESH:C579922), MDR (MESH:D018088)
- **Chemicals:** chloramphenicol (MESH:D002701), AMP (MESH:D000249), C (MESH:D002244), FEP (MESH:D011138), meropenem (MESH:D000077731), BPW (-), cefuroxime (MESH:D002444), carbapenems (MESH:D015780), agar (MESH:D000362), glycerol (MESH:D005990), amoxicillin-clavulanic acid (MESH:D019980), cefepime (MESH:D000077723), ceftriaxone (MESH:D002443), ampicillin (MESH:D000667), cefotaxime (MESH:D002439), aminoglycosides (MESH:D000617), carbonate (MESH:D002254), fluoroquinolones (MESH:D024841), salt (MESH:D012492), lactose (MESH:D007785), cephalosporins (MESH:D002511), ciprofloxacin (MESH:D002939), TE (MESH:D013691), saline (MESH:D012965), sulfamethoxazole-trimethoprim (MESH:D015662), gentamicin (MESH:D005839), Water (MESH:D014867), tetracycline (MESH:D013752), cellulose (MESH:D002482)
- **Species:** Enterobacterales (order) [taxon 91347], Vibrionales (order) [taxon 135623], Acinetobacter soli (species) [taxon 487316], V. albensis [taxon 140100], C. minuta [taxon 212553], Homo sapiens (human, species) [taxon 9606], Aeromonas veronii (species) [taxon 654], Leclercia adecarboxylata (species) [taxon 83655], Escherichia coli ATCC 25922 (strain) [taxon 1322345], Aeromonas hydrophila (species) [taxon 644], Enterobacter (genus) [taxon 547], Vibrio metschnikovii (species) [taxon 28172], Enterobacteriaceae (enterobacteria, family) [taxon 543], Culicoides arakawae (biting midge, species) [taxon 198116], Calidris minuta (species) [taxon 670340], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028371/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028371/full.md

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Source: https://tomesphere.com/paper/PMC13028371