# Comparative analysis of stress markers, metabolic health, and gut microbiota in healthy and disabled dogs in long-term shelters in Thailand

**Authors:** Adul Saengthong, Janine L. Brown, Patcharapa Towiboon, Khanittha Punturee, Songphon Buddhasiri, Korakot Nganvongpanit, Veerasak Punyapornwithaya, Wuithipong Tocharoennirattisai, Jaruwan Khonmee

PMC · DOI: 10.1371/journal.pone.0344383 · PLOS One · 2026-03-13

## TL;DR

This study compares stress, metabolism, and gut health in healthy and disabled dogs in Thai shelters, finding hidden health differences in disabled dogs.

## Contribution

The study reveals subclinical metabolic and microbial differences in disabled dogs despite similar stress levels, suggesting improved welfare monitoring methods.

## Key findings

- Disabled dogs had elevated oxidative stress markers and altered glucose and lipid profiles.
- Disabled dogs showed a reduced Firmicutes-to-Bacteroidetes ratio and lower beneficial gut bacteria.
- Stress hormone levels were similar between healthy and disabled dogs.

## Abstract

Regular welfare assessments are essential for identifying and addressing the physical, behavioral, and emotional needs of shelter dogs, thereby ensuring their well-being and improving chances for adoption or long-term stability within the shelter environment. This study compared biomarkers of physiological stress [fecal glucocorticoid metabolites (fGCM)], metabolic status [serum malondialdehyde (MDA), glucose, triglycerides, low- (LDL) and high- (HDL) density lipoproteins], and fecal microbiota composition over a 1-month period in healthy and spinal-injured disabled dogs housed in a large dog rescue shelter in Thailand for over 1 year. No significant differences in fGCM concentrations were observed between groups, indicating comparable levels of physiological stress in healthy and disabled dogs under long-term shelter conditions. In contrast, disabled dogs exhibited significant metabolic and oxidative alterations, including elevated MDA and glucose, along with lower triglyceride and HDL concentrations. Microbial analyses revealed comparable alpha diversity but differences in beta diversity between groups. Notably, disabled dogs exhibited a reduced Firmicutes-to-Bacteroidetes (F/B) ratio and decreased relative abundances of beneficial taxa such as Peptostreptococcaceae. These findings suggest that, despite comparable hormonal stress indicators, disabled dogs may experience subclinical physiological shifts that warrant more nuanced welfare monitoring. A multifactorial assessment incorporating metabolic and microbial parameters is recommended to ensure comprehensive welfare evaluation for physically impaired shelter dogs.

## Linked entities

- **Chemicals:** malondialdehyde (PubChem CID 10964), glucose (PubChem CID 5793), HDL (PubChem CID 6323542)
- **Diseases:** spinal injury (MONDO:0037747)
- **Species:** Canis lupus familiaris (taxon 9615)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 483665], INS (insulin) [NCBI Gene 280829], LOC442975 (mucin) [NCBI Gene 442975], CRP (C-reactive protein) [NCBI Gene 488629]
- **Diseases:** dysbiosis (MESH:D064806), spinal fractures and dislocations (MESH:D000072039), impaired lipid metabolism (MESH:D052439), gastrointestinal disorders (MESH:D005767), impaired mitochondrial function (MESH:D028361), reduction in HDL (MESH:D052456), psychological distress (MESH:D012128), irritable bowel syndrome (MESH:D043183), amputations (MESH:C565682), injury (MESH:D014947), impaired (MESH:D060825), mobility impairment (MESH:D014086), fGCM (MESH:C564221), obesity (MESH:D009765), metabolic function (MESH:D024821), chronic inflammation (MESH:D007249), inflammatory protein-losing enteropathy (MESH:D011504), metabolic disorders (MESH:D008659), condition (MESH:D020763), bed sores (MESH:D003668), chronic (MESH:D002908), paralysis (MESH:D010243), visual or auditory impairments (MESH:D014786), impaired locomotion (MESH:D020233), physical (MESH:D059445), aggression (MESH:D010554), spinal-injured disabled (MESH:D009069)
- **Chemicals:** TBA (MESH:C029684), MDA (MESH:D015104), Triglycerides (MESH:D014280), lipid (MESH:D008055), H2SO4 (MESH:C033158), cortisol (MESH:D006854), cholesterol (MESH:D002784), CHOD-PAP (-), agarose (MESH:D012685), lactic acid (MESH:D019344), ethanol (MESH:D000431), MDA (MESH:D008315), nitroblue tetrazolium (MESH:D009580), corticosterone (MESH:D003345), TC (MESH:D013667), carbohydrate (MESH:D002241), water (MESH:D014867), short-chain fatty acid (MESH:D005232), glucose (MESH:D005947), Butyrate (MESH:D002087), TMB (MESH:C021758), 1,1,3,3-tetramethoxypropane (MESH:C041295), reactive oxygen species (MESH:D017382), fructosamine (MESH:D019270), methanol (MESH:D000432), phosphoric acid (MESH:C030242)
- **Species:** Streptococcus (genus) [taxon 1301], Homo sapiens (human, species) [taxon 9606], Prionailurus bengalensis (leopard cat, species) [taxon 37029], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Bos taurus (bovine, species) [taxon 9913], Rodentia (rodent, order) [taxon 9989], Mus musculus (house mouse, species) [taxon 10090], Panthera tigris (tiger, species) [taxon 9694], gut metagenome (species) [taxon 749906], Fusobacteriia (class) [taxon 203490], Lactobacillus (genus) [taxon 1578], Prevotella (genus) [taxon 838], Sciurus vulgaris (Eurasian red squirrel, species) [taxon 55149], Bacteroidia (class) [taxon 200643], Panthera leo (lion, species) [taxon 9689], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Canis lupus familiaris (dog, subspecies) [taxon 9615], Peptoclostridium (genus) [taxon 1481960]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987422/full.md

## References

92 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987422/full.md

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Source: https://tomesphere.com/paper/PMC12987422