Effect of in ovo administration of an adult-derived microbiota on establishment of the intestinal microbiome in chickens.

OBJECTIVE To determine effects of in ovo administration of a probiotic on development of the intestinal microbiota of 2 genetic lineages (modern and heritage) of chickens. SAMPLE 10 newly hatched chicks and 40 fertile eggs to determine intestinal microbiota at hatch, 900 fertile eggs to determine effects of probiotic on hatchability, and 1,560 chicks from treated or control eggs. PROCEDURES A probiotic competitive-exclusion product derived from adult microbiota was administered in ovo to fertile eggs of both genetic lineages. Cecal contents and tissues were collected from embryos, newly hatched chicks, and chicks. A PCR assay was used to detect bacteria present within the cecum of newly hatched chicks. Fluorescence in situ hybridization and vitality staining were used to detect viable bacteria within intestines of embryos. The intestinal microbiota was assessed by use of 16S pyrosequencing. RESULTS Microscopic evaluation of embryonic cecal contents and tissues subjected to differential staining techniques revealed viable bacteria in low numbers. Development of the intestinal microbiota of broiler chicks of both genetic lineages was enhanced by in ovo administration of adult microbiota. Although the treatment increased diversity and affected composition of the microbiota of chicks, most bacterial species present in the probiotic were transient colonizers. However, the treatment decreased the abundance of undesirable bacterial species within heritage lineage chicks. CONCLUSIONS AND CLINICAL RELEVANCE In ovo inoculation of a probiotic competitive-exclusion product derived from adult microbiota may be a viable method of managing development of the microbiota and reducing the prevalence of pathogenic bacteria in chickens.

Egg yolk fatty acid profile in relation to dietary fatty acid concentrations.

BACKGROUND: The health benefits of n-3 fatty acids have led to much research on manipulating the fatty acid composition of animal-derived foods. In this study, two experiments were conducted to investigate the interaction of dietary fatty acids on egg yolk fatty acid concentrations. In experiment I, 32 dietary treatments with three replicates of three birds each were fed for 35 days. Diets were prepared by mixing one type of fish oil with four vegetable oils in different proportions. In experiment II, three different types and two levels of fish oil in combination with two vegetable oils were tested under the same conditions as in experiment I. RESULTS: In experiment I the results showed that the egg yolk saturated (SFA) and monounsaturated (MUFA) fatty acid concentration was determined by the dietary SFA, MUFA and 18:2n-6 content. The egg 18:2n-6 concentration was mainly explained by the dietary inclusion of 18:2n-6 and negatively by the dietary MUFA content. The egg C18:3n-3, C20:5n-3 and C22:6n-3 concentration is almost exclusively determined by their direct supply from the diet. The egg 20:4n-6 concentration was inversely proportional to the long-chain n-3 polyunsaturated fatty acid content of the diet. The results of experiment II showed that the egg yolk C20:5n-3 and C22:6n-3 concentration was determined by both the level of dietary fish oil (1 or 2%) and the C20:5n-3/C22:6n-3 ratio in the fish oil. CONCLUSION: The results of this study demonstrated that the direct dietary supply of fatty acids is the most important factor determining the egg yolk fatty acid composition, in particular for the n-3 fatty acids. The interaction effect from other dietary fatty acids was in general small.