Altitude-dependent agro-ecologies impact the microbiome diversity of scavenging indigenous chicken in EthiopiaOriginal paper
What was studied?
This study characterized the caecal gut microbiota of scavenging indigenous village chickens across Ethiopia's varied altitude-dependent agro-ecologies. Researchers used shotgun metagenomics on caecal content samples collected from many villages and districts. They built a non-redundant gene catalogue of over 33 million genes, assembled metagenome-assembled genomes, defined enterotypes, and linked microbiota to climate, topsoil, and farmer-supplied supplementary diets.
Who was studied?
The samples came from 243 Ethiopian indigenous scavenging chickens, of which 240 passed quality control. Birds were sampled from 26 sites across 15 districts, spanning wide ranges of latitude, longitude, and altitude. Five climate zones were defined, with altitude and mean annual temperature as major predictors. These free-ranging birds differ sharply from grain-fed commercial breeds raised in biosecure facilities, giving a rare view of naturally adapted poultry microbiomes.
What were the most important findings?
Bacteroidota was the most abundant phylum (48.0 percent), followed by Firmicutes (32.9 percent). The microbiota clustered into three enterotypes, with enterotype 3 dominating high-altitude zone 1 (62 percent of samples). Chickens above 3000 m carried more than 2.5-fold higher Bacteroides (17.6 percent). Diversity decreased significantly as altitude rose. The team assembled 9977 strain-level genomes; 9682 strains and 1242 species were absent from prior chicken datasets and the Genome Taxonomy Database. Most species-level genomes carried at least one antimicrobial resistance gene, most often for tetracycline.
What are the greatest implications of this study?
The work greatly expands the known microbial diversity of poultry, showing scavenging village chickens host thousands of previously uncatalogued microbes. Altitude, temperature, precipitation, topsoil, and supplementary grains all shaped the gut microbiota, arguing that local environment drives microbial adaptation. The rich carbohydrate-active enzyme repertoire may support digestion of diverse scavenged fibers. These genomes are a resource for improving indigenous poultry nutrition and disease resistance, though the observational design cannot prove that specific microbes cause the observed adaptations.