Abstract

While conventionally grown poultry continues to dominate the U. S. poultry industry, there is an increasing demand for locally-grown, “all natural” alternatives. The use of next generation sequencing allows for not only the gross (e.g., community structure) but also fine-scale (e.g., taxa abundances) examination of these complex microbial communities. This data provides a better understanding of how a pasture flock's microbiome changes throughout the production life cycle and how that change in microbial ecology changes foodborne pathogens in alternative poultry production systems. In order to understand this ecology better, pooled broiler samples were taken during the entire flock life cycle, from pre-hatch gastrointestinal samples (N = 12) to fecal samples from the brood (N = 5), and pasture (N = 10) periods. Additional samples were taken during processing, including skin and feather rinsates (N = 12), ceca (N = 12), and whole carcass rinses (N = 12), and finally whole carcasss rinsates of final products (N = 3). Genomic DNA was extracted, 16S rDNA microbiome sequencing was conducted (Illumina MiSeq), and microbiomes were analyzed and compared using QIIME 1.9.1 to determine how microbiomes shifted throughout production continuum, as well as what environmental factors may be influencing these shifts. Significant microbiome shifts occurred during the life cycle of the pasture broiler flock, with the brood and pasture fecal samples and cecal samples being very distinct from the other pre-hatch, processing, and final product samples. Throughout these varied microbiomes, there was a stable core microbiome containing 13 taxa. Within this core microbiome, five taxa represented known foodborne pathogens (Salmonella, Campylobacter) or potential/emerging pathogens (Pseudomonas, Enterococcus, Acinetobacter) whose relative abundances varied throughout the farm-to-fork continuum, although all were more prevalent in the fecal samples. Additionally, of the 25 physiochemical and nutrient variables measured from the fecal samples, the carbon to nitrogen ratio was one of the most significant variables to warrant further investigations because it impacted both general fecal microbial ecology and Campylobacter and Enterococcus taxa within the core fecal microbiomes. These findings demonstrate the need for further longitudinal, farm-to-fork studies to understand the ecology of the microbial ecology of pasture production flocks to improve animal, environmental, and public health.

Highlights

  • The gastrointestinal tract (GIT) of poultry hosts a complex and dynamic bacterial microbiota [1], and these microbial communities can directly affect animal, environmental, and public health [2, 3]

  • Studies have shown that environmental factors such as hatchery hygiene levels [4], housing [5], and production system [6, 7], litter quality and management [8, 9], and climate and geographical locations [10, 11] can significantly influence poultry GIT microbiota and the diversity demonstrate the dynamics of GIT microbial ecology

  • Previous poultry-related microbiome work has not shown any associations between Campylobacter to other bacterial microbiome taxa [23], but this current study shows that C:N ratio is significantly correlated to Campylobacter and Enterococcus, and was shown to have a significant effect of the β-diversity distribution of the total fecal microbiomes (Figure 3)

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Summary

Introduction

The gastrointestinal tract (GIT) of poultry hosts a complex and dynamic bacterial microbiota [1], and these microbial communities can directly affect animal, environmental, and public health [2, 3]. While zoonotic pathogen colonization can occur at any stage of the farm-to-fork continuum, the lack of a mature GIT microbial ecology makes newly-hatched chicks susceptible [17]. The source of these pathogens that colonize juvenile birds are from the surrounding farm environment [18, 19], and from the other chickens within a flock [20, 21]. It is important to attempt to understand these longitudinal dynamics from farm-to-fork

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