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Background <p>Mixed strongyle infections represent the most prevalent equine parasitosis and can result in life-threatening disease, especially in young horses. Species involvement and pathogenesis of this parasitosis are poorly understood, and data on foals and broodmares are notably lacking.</p> Methods <p>In a longitudinal study undertaken in 2022 in Germany, individual faecal samples (<i>n</i> = 497) and metadata were collected for naturally infected foals and broodmares (<i>n</i> = 48) kept under conventional husbandry conditions. Nematode infections were detected coproscopically via the Mini-FLOTAC method. In a subset of strongyle egg-positive samples (<i>n</i> = 46), species were identified using cytochrome <i>c</i> oxidase subunit I deep amplicon sequencing. Species prevalence, richness, and alpha and beta diversity were compared between foals and mares.</p> Results <p>Overall, 22.2% of the foal samples and 10.2% of the mare samples were strongyle egg positive (eggs per gram &gt; 5). <i>Parascaris</i> spp. were only detected in foals (15.1%). <i>Strongyloides westeri</i> was detected in one foal sample. Strongyle egg detection increased in likelihood with each additional sample timepoint (OR = 1.42, <i>P</i> &lt; 0.001) and with ascarid egg detection (OR = 6.49, <i>P</i> &lt; 0.001), while last anthelmintic treatment with pyrantel decreased the odds of detecting eggs (OR = 0.12, <i>P</i> = 0.002). Deep amplicon sequencing detected 16 species of small strongyles but no large strongyle species. <i>Cylicostephanus goldi, Cylicostephanus minutus</i> operational taxonomic unit II and <i>Cylicocyclus ashworthi</i> were significantly more prevalent in mares (<i>P</i> &lt; 0.05), while <i>Cylicostephanus calicatus</i> operational taxonomic unit II was more prevalent in foals (<i>P</i> &lt; 0.01). Mares showed a significantly higher amplicon sequence-variant-based richness (Chao 1 index, <i>P</i> &lt; 0.001) and diversity (inverse Simpson index, <i>P</i> &lt; 0.01) than foals. Group (foals vs. mares) explained some of the variance in beta diversity, according to permutational multivariate ANOVA. Co-infection with <i>Parascaris</i> spp. did not affect strongyle community composition in the foals. Bray–Curtis and Jaccard distance (dissimilarity) plots showed separate clusters for mares and foals, with some overlap and a moderate model fit.</p> Conclusions <p>Cytochrome oxidase-based characterization of mixed strongyle infections revealed strongyle community differences between broodmares and foals. Possible age associations were identified for four species of small strongyles, including two cryptic species. Low overall strongyle prevalence and egg-shedding intensity, non-random sampling and differences in anthelmintic treatment schemes limited the statistical power of this study.</p> Graphical Abstract <p></p>

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Characterizing mixed strongyle infections in foals and broodmares using cytochrome c oxidase subunit I deep amplicon sequencing

  • 期刊论文

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  • 发表日期：

    2026年1月3日

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  • Luise Grace Klass,
  • Jürgen Krücken,
  • Susan Mbedi,
  • Sarah Sparmann,
  • Thore Schenk,
  • Sandro Andreotti,
  • Georg von Samson-Himmelstjerna

摘要

Background

Mixed strongyle infections represent the most prevalent equine parasitosis and can result in life-threatening disease, especially in young horses. Species involvement and pathogenesis of this parasitosis are poorly understood, and data on foals and broodmares are notably lacking.

Methods

In a longitudinal study undertaken in 2022 in Germany, individual faecal samples (n = 497) and metadata were collected for naturally infected foals and broodmares (n = 48) kept under conventional husbandry conditions. Nematode infections were detected coproscopically via the Mini-FLOTAC method. In a subset of strongyle egg-positive samples (n = 46), species were identified using cytochrome c oxidase subunit I deep amplicon sequencing. Species prevalence, richness, and alpha and beta diversity were compared between foals and mares.

Results

Overall, 22.2% of the foal samples and 10.2% of the mare samples were strongyle egg positive (eggs per gram > 5). Parascaris spp. were only detected in foals (15.1%). Strongyloides westeri was detected in one foal sample. Strongyle egg detection increased in likelihood with each additional sample timepoint (OR = 1.42, P < 0.001) and with ascarid egg detection (OR = 6.49, P < 0.001), while last anthelmintic treatment with pyrantel decreased the odds of detecting eggs (OR = 0.12, P = 0.002). Deep amplicon sequencing detected 16 species of small strongyles but no large strongyle species. Cylicostephanus goldi, Cylicostephanus minutus operational taxonomic unit II and Cylicocyclus ashworthi were significantly more prevalent in mares (P < 0.05), while Cylicostephanus calicatus operational taxonomic unit II was more prevalent in foals (P < 0.01). Mares showed a significantly higher amplicon sequence-variant-based richness (Chao 1 index, P < 0.001) and diversity (inverse Simpson index, P < 0.01) than foals. Group (foals vs. mares) explained some of the variance in beta diversity, according to permutational multivariate ANOVA. Co-infection with Parascaris spp. did not affect strongyle community composition in the foals. Bray–Curtis and Jaccard distance (dissimilarity) plots showed separate clusters for mares and foals, with some overlap and a moderate model fit.

Conclusions

Cytochrome oxidase-based characterization of mixed strongyle infections revealed strongyle community differences between broodmares and foals. Possible age associations were identified for four species of small strongyles, including two cryptic species. Low overall strongyle prevalence and egg-shedding intensity, non-random sampling and differences in anthelmintic treatment schemes limited the statistical power of this study.

Graphical Abstract