ArticlePoultry science2025
Probiotic application to hatching egg surface supports microbiota development and acquisition in broiler embryos and hatchlings.
Article in Poultry science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Mechanisms of probiotic action in poultry gut: Colonization resistance, bioactive metabolites, quorum sensing activity, and immunomodulation.Poultry science · 2026Review
- Mechanistic insights into probiotic modulation of the gut-immune axis and their role as sustainable antibiotic alternatives in poultry production: An integrative review.Veterinary world · 2026Article
- Low-Fat Cheddar Cheese Influences Gut Microbiota Composition and Diversity in Human Microbiota-Associated Mice.Foods (Basel, Switzerland) · 2025Article
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
In modern poultry production, hatchlings primarily acquire their initial gut microbiota from the hatchery environment. This, in turn, results in delayed gut microbiota acquisition and a less diverse microbiota. However, the gut microbiota in the hatchling and the neonate is crucial for the normal development of the immune system and healthy gut function. Hence, promoting healthy microbiota development and acquisition in hatchlings is critical. To this end, we determined the potential for probiotic spray application to hatching eggs to support microbiota acquisition in the hatchling. A total of 100 hatching eggs (Ross 308) were either sprayed with phosphate-buffered saline (PBS; Control) or probiotics [∼9 log CFU/egg of Lacticaseibacillus rhamnosus NRRL B-442 (LR) or Lacticaseibacillus paracasei DUP 13076 (LP)] during incubation. Six eggs were sacrificed for sample collection at each sampling point. Eggshells were washed with sterile PBS buffer and collected at embryonic day (D) 0, 7, 14, 18, and 20. Chorioallantoic membrane (CAM) was collected at D7, 14, 18, and 20, and intestine at D14, 18, and 20. At hatch, chicks were euthanized, and the cecal and ileal samples were collected for microbiota characterization. Results indicate that spray application of LP and LR significantly modulated the microbiota associated with the eggshell, CAM, embryonic intestine, and hatchling gut. Further predictive analysis revealed CAM to be a significant source for the microbiota associated with the hatchling gut. Also, application of LP and LR led to significant enrichment in Lactobacillus populations and potential probiotic taxa, including Enterococcus, in the hatchling gut. Moreover, functional profile analysis revealed that microbial communities associated with the hatchling gut microbiota in the probiotic groups were enriched for nutrient and energy metabolism, which could not only support embryo development but also post-hatch growth. In conclusion, in ovo spray application of probiotics to the egg's surface can be a potential approach to support microbiota acquisition in hatchlings.
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