Browsing by Person "Philippi, Hanna"

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Methane reduction potential of brown seaweeds and their influence on nutrient degradation and microbiota composition in a rumen simulation technique
(2022) Künzel, Susanne; Yergaliyev, Timur; Wild, Katharina J.; Philippi, Hanna; Petursdottir, Asta H.; Gunnlaugsdottir, Helga; Reynolds, Chris K.; Humphries, David J.; Camarinha-Silva, Amélia; Rodehutscord, Markus
This study aimed to investigate the effects of two brown Icelandic seaweed samples (Ascophyllum nodosum and Fucus vesiculosus) on in vitro methane production, nutrient degradation, and microbiota composition. A total mixed ration (TMR) was incubated alone as control or together with each seaweed at two inclusion levels (2.5 and 5.0% on a dry matter basis) in a long-term rumen simulation technique (Rusitec) experiment. The incubation period lasted 14 days, with 7 days of adaptation and sampling. The methane concentration of total gas produced was decreased at the 5% inclusion level of A. nodosum and F. vesiculosus by 8.9 and 3.6%, respectively (P < 0.001). The total gas production was reduced by all seaweeds, with a greater reduction for the 5% seaweed inclusion level (P < 0.001). Feed nutrient degradation and the production of volatile fatty acids and ammonia in the effluent were also reduced, mostly with a bigger effect for the 5% inclusion level of both seaweeds, indicating a reduced overall fermentation (all P ≤ 0.001). Microbiota composition was analyzed by sequencing 16S rRNA amplicons from the rumen content of the donor cows, fermenter liquid and effluent at days 7 and 13, and feed residues at day 13. Relative abundances of the most abundant methanogens varied between the rumen fluid used for the start of incubation and the samples taken at day 7, as well as between days 7 and 13 in both fermenter liquid and effluent (P < 0.05). According to the differential abundance analysis with q2-ALDEx2, in effluent and fermenter liquid samples, archaeal and bacterial amplicon sequence variants were separated into two groups (P < 0.05). One was more abundant in samples taken from the treatment without seaweed supplementation, while the other one prevailed in seaweed supplemented treatments. This group also showed a dose-dependent response to seaweed inclusion, with a greater number of differentially abundant members between a 5% inclusion level and unsupplemented samples than between a 2.5% inclusion level and TMR. Although supplementation of both seaweeds at a 5% inclusion level decreased methane concentration in the total gas due to the high iodine content in the seaweeds tested, the application of practical feeding should be done with caution.
Zinc supplementation effects on phytate degradation, mineral digestibility, and bone characteristics in broiler chickens
(2024) Philippi, Hanna; Rodehutscord, Markus
An adequate supply of phosphorus (P) is important in poultry nutrition, as P is essential for numerous metabolic processes. However, oversupply should be avoided to reduce the environmental impact of poultry production. The main source of P in plant feedstuffs commonly used in poultry nutrition is phytate, the salt form of phytic acid (InsP6). For P from InsP6 to be utilized by animals, it needs to be cleaved by phytases or other phosphatases. However, the capacity of endogenous phosphatases of non-ruminant animals does not suffice to release sufficient P to fulfill the animal’s P requirement. Therefore, commercial poultry diets usually are supplemented with P from mineral sources. By using exogenous phytases, the supplementation of mineral P can be reduced, and finite P reserves can be conserved. To feed poultry without mineral P in the future, phytase efficacy must be improved further. Thus, it is important to know and understand all factors influencing phytase efficacy. The results of in vitro studies have indicated that zinc (Zn) may be an influencing factor. The supplementation of Zn could inhibit phytase activity, with the degree of inhibition depending on the exogenous Zn source used. A literature review on the interactions of Zn with phytate and phytase (Manuscript A of this thesis) has identified a lack of in vivo studies investigating the effects of Zn supplementation on phytase with direct measurements, such as intestinal phytate degradation and prececal P digestibility. Therefore, three in vivo studies were conducted as part of this thesis with the main objective to investigate the effect of Zn supplementation and exogenous Zn source on intestinal phytate degradation in broiler chickens. It was hypothesized that due to the formation of insoluble complexes of Zn and phytate, the supplementation of Zn could reduce phytase efficacy with the extent of reduction depending on the exogenous Zn source. Further, other traits that are affected by Zn supply, such as bone mineralization and gene expression, were also investigated in these in vivo studies. The first experiment (Manuscript B) aimed to determine the effect of dietary Zn level and source on intestinal phytate breakdown, mineral digestibility, bone mineralization, and Zn status without and with exogenous phytase in the feed. Ross 308 broiler chickens were fed experimental diets from day 7 to 28. The basal diet contained 33 mg/kg dry matter native Zn and a high phytate-P concentration to challenge interactions in the digestive tract. The experimental diets differed in the level of exogenous phytase (0 or 750 FTU/kg) and in the Zn source (none, 30 mg/kg of Zn-sulfate, or 30 mg/kg of Zn-oxide). Additionally, two experimental diets with a high Zn supplementation level (90 mg/kg) in the form of Zn-sulfate or Zn-oxide, both containing exogenous phytase, were tested. Intestinal phytate breakdown, P digestibility, and bone mineralization were not affected by Zn source or Zn level but only by phytase supplementation. The concentration of ileal myo-inositol was influenced by phytase × Zn source interaction. Birds fed without phytase supplementation had similarly low myo-inositol concentrations whether they received Zn supplementation or not, whereas birds receiving phytase supplementation and Zn supplementation had significantly higher ileal myo-inositol concentrations than birds fed without Zn supplementation but with phytase supplementation. The missing effect of Zn level or Zn source on phytate degradation indicates that no interactions of Zn and phytate relevant for phytase efficacy occurred in the digestive tract of broilers when Zn was supplemented at levels up to 90 mg/kg in the form of Zn-sulfate or Zn-oxide. Based on the results of the first experiment, where Zn alone did not show relevant interactions with phytate, the second experiment (Manuscript C) aimed to investigate whether the combined supplementation of Zn, copper (Cu), and manganese (Mn) from different sources without and with exogenous phytase in the feed affects intestinal phytate breakdown, prececal mineral digestibility, bone mineralization, and mRNA expression of mineral transporters. Cobb 500 broiler chickens received experimental diets from day 0 to 28. Experimental diets differed in the level of phytase supplementation (0 or 750 FTU/kg) and in the trace mineral source (TMS: 100 mg/kg Zn, 100 mg/kg Mn, and 125 mg/kg Cu as sulfates, oxides, or chelates). Prececal InsP6 disappearance and P digestibility were significantly affected by phytase × TMS interaction. Whereas birds receiving exogenous phytase had similar InsP6 disappearance and P digestibility irrespective of TMS, birds fed without exogenous phytase and with chelated trace minerals had a higher InsP6 disappearance and P digestibility than birds receiving no exogenous phytase and oxides or sulfates. These results indicate that the combined supplementation of Zn, Mn, and Cu at high levels may challenge interactions with phytate in non-phytase-supplemented diets with the extent of interaction depending on the TMS. In phytase-supplemented diets however, the choice of TMS was irrelevant for phytate degradation under the conditions of this study. The third experiment (Manuscript D) aimed to determine the impact of Zn level and Zn source on prececal phytate degradation, mineral digestibility, bone mineralization, and mRNA expression of intestinal (trace) mineral transporters. In contrast to the first experiment, an inorganic Zn source and a chelated Zn source were tested. Cobb 500 broiler chickens received experimental diets from day 0 to 21. The experimental diets differed in Zn supplementation level (10, 30, 50 mg/kg Zn) and exogenous Zn source (Zn-oxide or Zn-glycinate). A cornsoybean meal-based diet without Zn supplementation containing 35 mg/kg native Zn was used as a control. All experimental diets were supplemented with 750 FTU/kg phytase. Prececal InsP6 disappearance, P digestibility, and tibia ash quantity and concentration, and Zn concentration in tibia ash were not affected by diet. Bone breaking strength and tibia width did not differ between treatments. Tibia thickness was lower in the treatments with 30 mg Zn as Zn-oxide and 50 mg Zn as Zn-glycinate than in the treatment with 10 mg Zn as Zn-oxide. The expression of intestinal (trace) mineral transporters was not affected by treatment. These results indicate that in phytase-supplemented diets the native Zn concentration of cornsoybean meal-based diets is satisfactory to achieve maximal Zn concentration in tibia ash during the first 3 weeks of age. The missing effect of Zn level or Zn source on phytate degradation confirms the results from Manuscript B, that Zn and phytate do not interact to a level relevant for phytate degradation by exogenous phytase. It is concluded that contrary to the hypothesis that Zn inhibits phytate degradation by complex formation with phytate, the Zn supplementation up to 100 mg/kg does not appear to influence exogenous phytase efficacy. Minor effects were found on the endogenous phytate degradation if Zn, Cu, and Mn were supplemented combined at high levels, where the extent of reduction in endogenous phytate degradation was dependent on the TMS. It remains unclear whether the inhibiting effect on endogenous phytate degradation occurs only due to the combined supplementation or whether an individual high supplementation of a single trace mineral caused the effect. Further experiments are needed to investigate the effect of Zn on endogenous phosphatases, where the activity of endogenous mucosal activity should be determined in broilers fed diets differing in the Zn supplementation level. Moreover, further experiments are needed to test what level of Zn supplementation is needed in phytase-supplemented diets to ensure the birds sufficient supply in all areas. Besides bone development and growth, effects on the immune system, microbiota composition, and the antioxidative system should be considered.