# Beyond the host: Unveiling the independent microbiome of equine gastrointestinal nematodes

## TL;DR

This study reveals that equine gastrointestinal nematodes have unique microbiomes distinct from their hosts, suggesting potential new ways to control these parasites.

## Contribution

The study identifies the structured and independent microbiome of equine gastrointestinal nematodes, offering insights for novel control strategies.

## Key findings

- Nematode microbiomes are dominated by Firmicutes, Proteobacteria, and other taxa distinct from host faecal microbiota.
- Microbial composition varies by intestinal site, nematode subfamily, and sex, with Proteobacteria enriched in the caecum.
- Core nematode-associated taxa include Fusobacterium, Mesorhizobium, and Mycoplasma, indicating ecological specialization.

## Abstract

Gastrointestinal nematode infections significantly impact equine health and welfare, with rising anthelmintic resistance demanding alternative control strategies. Emerging evidence suggests that parasitic nematodes harbour distinct microbiomes, potentially influencing host-parasite dynamics and parasite survival. This study aimed to characterize and compare the microbiomes of equine gastrointestinal nematodes and their hosts, focusing on differences in composition, diversity, and core microbiota structure across different intestinal sites, nematode subfamilies, and sexes. Faecal and nematode samples were collected from equids (Equus caballus and Equus asinus) at slaughterhouses. DNA was extracted, and the V3-V4 regions of the 16S rRNA gene were amplified and sequenced using the Illumina iSeq 100 platform. Bioinformatic analyses were performed with QIIME2 and MicrobiomeAnalyst, and statistical comparisons employed PERMANOVA, LEfSe, and alpha and beta diversity metrics. Nematodes exhibited a distinct microbiome dominated by Firmicutes, Proteobacteria, Bacteroidota, Verrucomicrobiota, and Actinobacteriota, differing significantly from the faecal microbiota. Alpha diversity analyses revealed lower richness in nematodes, while beta diversity indicated distinct community structures (p = 0.007). Microbial composition varied by gastrointestinal site, nematode subfamily, and sex. Proteobacteria were consistently enriched in nematodes, particularly in the caecum. Core microbiome analysis identified exclusive nematode-associated taxa such as Fusobacterium, Mesorhizobium, and Mycoplasma. Equine gastrointestinal nematodes harbour independent and structured microbiomes, distinct from those of their hosts. These findings underscore the ecological specialization of nematodes and highlight the potential of targeting parasite-associated microbiota for novel control strategies.