Research Note: Preliminary assessment of the impact of dietary yeast products on egg production and cecal microbial profiles of laying hens.

The objective of the current study was to conduct an initial comparison of commercial yeast products in layer hen diets on egg production parameters and the corresponding impact on the cecal microbiota. A short-term feeding study was conducted with 35 laying hens receiving either a control, or 1 of 4 different yeast fermentation products, Immunowall, Hilyses (both from ICC, São Paulo, Brazil), Citristim (ADM, Decatur, IL), and Maxi-Gen Plus (CBS Bio Platforms, Calgary, Canada) with 7 hens per treatment from 40 to 46 wk of age. At the end of the trial, hens were euthanized, the ceca removed and prepared for denatured gradient gel electrophoresis (DGGE) microbial compositional analyses. Although initial shell weight and shell thickness were similar among the treatment groups, hens fed Hilyses had lower shell weight and thickness at the end of the experiment. The most predominant DGGE bands with the strongest intensity were identified as Lactobacillus species and excised double bands were identified as Bacillus, Clostridium, or Lachnospiraceae. In this short-term feeding trial, the commercial yeast products tested had little effect on egg production and shell quality, and only moderately impacted the composition of mature layer hen cecal microbiota.

Effect of hen age and maternal vitamin D source on performance, hatchability, bone mineral density, and progeny in vitro early innate immune function.

The metabolite 25-hydroxy vitamin D3 (25-OHD) can complement or replace vitamin D3 in poultry rations, and may influence broiler production and immune function traits. The effect of broiler breeder dietary 25-OHD on egg production, hatchability, and chick early innate immune function was studied. We hypothesized that maternal dietary 25-OHD would support normal broiler breeder production and a more mature innate immune system of young chicks. Twenty-three-week-old Ross 308 hens (n=98) were placed in 4 floor pens and fed either 2,760 IU vitamin D3 (D) or 69 µg 25-OHD/kg feed. Hen weights were managed according to the primary breeder management guide. At 29 to 31 wk (Early), 46 to 48 wk (Mid), and 61 to 63 wk (Late), hens were artificially inseminated and fertile eggs incubated and hatched. Chicks were placed in cages based on maternal treatment and grown to 7 d age. Innate immune function and plasma 25-OHD were assessed at 1 and 4 d post-hatch on 15 chicks/treatment. Egg production, hen BW, and chick hatch weight were not affected by diet (P>0.05). Total in vitro Escherichia coli (E. coli) killing by 25-OHD chicks was greater than the D chicks at 4 d for the Early and Mid hatches, and 1 and 4 d for the Late hatch. This can be partly explained by the 25-OHD chicks from the Late hatch also having a greater E. coli phagocytic capability. No consistent pattern of oxidative burst response was observed. Chicks from the Mid hatch had greater percent phagocytosis, phagocytic capability, and E. coli killing than chicks from Early and Late hatches. Overall, maternal 25-OHD increased hatchability and in vitro chick innate immunity towards E. coli. Regardless of treatment, chicks from Late and Early hens had weaker early innate immune responses than chicks from Mid hens. The hen age effect tended to be the greatest factor influencing early chick innate immunity, but maternal 25-OHD also increased several measures relative to D.

The effect of calcium source and particle size on the production performance and bone quality of laying hens.

The efficacy of 3 local limestone sources as potential Ca sources for laying hens was studied. Limestone sources were assessed for in vitro solubility. Four Ca sources (control, A, B, or C) and 2 particle size combinations (ground, 100% ground; or mixed, 67% ground+33% large particle) was used. The control consisted of a commercial ground limestone for the ground Ca source and oyster shell of the large particle Ca source. DeKalb laying hens were randomly placed in 32 battery cage units (n=12/cage). At 19 wk of age, hens received 1 of 8 Ca source and particle size treatments (4 replicates/treatment) until 74 wk. Egg production, feed consumption, BW, and egg quality were measured throughout. Bone mineral density (by quantitative computed tomography), breaking strength, ash, and Ca were assessed at the end of lay. In vitro solubility was dependent upon Ca source and particle size (P<0.0001) with oyster shell generally having a greater in vitro solubility than test limestone sources A, B, and C of similar particle sizes. Feed consumption (100 to 117 g/bird per day), BW (1,500 to 1,800 g), egg production (92% peak egg production), egg weight (55 to 67 g), and egg specific gravity (1.090 to 1.078) did not differ among hens fed the different Ca sources (P>0.05). Tibia bone mineral density indicated the oyster shell treatment had a lower trabecular density than Ca source A; however, all other Ca sources had similar bone mineral density for all measures (P>0.05). Hens fed the mixed Ca particle treatments consistently had greater feed consumption from 27 to 70 wk than those fed the 100% ground Ca source (P<0.05). Bone mineralization was enhanced in hens that received the mixed Ca particle treatments (P<0.05). Overall, the results of this study indicate that the local limestone sources A, B, and C would be suitable alternatives to current commercial sources of Ca for laying hens. In addition, large particle Ca did improve bone quality.

End-of-cycle bone quality in white- and brown-egg laying hens.

Broken and weak bones of laying hens are major welfare concerns in the table egg industry. Bone quality at the end of lay of brown- (Shaver 579) and white-(Shaver 2000) egg strains were compared. Prior to the start of the experiment, the hens had been housed in laying hen cages (2/cage). At 423 d of age (60 wk + 3 d), 24 hens of each strain were selected and individually caged, and egg production records were kept until 462 d of age (the end of 65 wk) for a total of 39 d. Egg quality analysis was undertaken during wk 65 of age. Hens were killed at 66 wk of age (463 d), and carcass and reproductive morphology traits were measured. Femur and humerus mineral density were measured using quantitative computed tomography, and breaking strength was measured by an Instron Materials Tester. The white-egg strain produced 3.7% more marketable eggs during the experiment due to a 0.3 d shorter mean pause length in egg production. Eggs from the brown strain were 3.4% heavier, had 4.0% more eggshell, and had a higher specific gravity than the white strain eggs (1.077 and 1.072, respectively). Final BW was 330 g greater in the brown-egg strain. Total bone density of the femur was not different between the 2 strains but was greater in the humerus of the brown-egg layers. Total femur and humerus bone areas were greater in the brown strain than the white-egg strain. Bone breaking strengths of the brown-egg strain were greater by 22% (femur) and 18% (humerus) than in the white-egg strain hens. These results indicate that this brown-egg strain may be more resistant to weak and broken bones at the end of production than the white-egg strain.

Assessing bone mineral density in vivo: quantitative computed tomography.

Egg-laying hens require substantial amounts of Ca to support eggshell formation. Over time, structural bone is catabolized to provide some of the Ca required; the structural bone is not replaced. As the hen ages, this can eventually lead to osteoporosis. Quantitative Computed Tomography (QCT) is a nondestructive technique used to measure bone mineral density (BMD). QCT is used diagnostically in humans to assess osteoporosis; BMD determined by QCT is correlated with other, more invasive methods of bone mineral determinations, such as ashing. An x-ray is sent through a bone at multiple angles within a plane to generate a 2-dimensional image and a 3-dimensional calculation of volume and BMD. The technique allows resolution of total, trabecular, and cortical BMD and cross-sectional areas. The separation of bone types allows very precise measurements of the bone compartments most important in Ca supply for eggshell formation and bone strength. QCT has been adapted in our laboratory to measure BMD in vivo and ex vivo in poultry; values obtained for poultry bones are moderately correlated with destructive means of assessing bone quality such as breaking strength, ashing, and chemical bone mineral determinations. Thus, changes in BMD of individual birds can be measured over time; BMD at specific time points can be correlated with production parameters and eggshell quality traits. QCT is an effective technique to measure BMD in laying hens, which allows resolution of total BMD as well as cortical and trabecular BMD.