Effects of novel organic sources of cobalt on ruminal fermentation, nutrient degradation and vitamin B12 synthesis in vitro

Cobalt (Co) is essential for vitamin B<sub>12</sub> synthesis in the rumen and energy metabolism in cattle. Previous studies on organic Co sources have shown variable effects on dairy cows' performance, focusing primarily on Co glucoheptonate as an alternative to the traditional Co carbonate (CoCO<sub>3</sub>). Our objective was to evaluate the effects of novel organic Co sources on ruminal microbial fermentation, nutrient degradation, and vitamin B<sub>12</sub> synthesis using a dual-flow continuous culture system. We used eight fermenters in a duplicated 4 × 4 Latin Square design, where each -fermenter was provided daily with 106 g DM of a basal diet plus the corresponding Co treatment. The treatments consisted of supplementing 1 mg Co/kg DM from the following Co sources: (i) CoCO<sub>3</sub>, (ii) Co Pectin (CoPec), (iii) Co Amino Acid (CoAA), and (iv) Co Pectin + Co Amino Acid (CoPec+CoAA). Data were analyzed with the MIXED procedure of SAS 9.4 to evaluate the effect of Co source on pH, VFA, N metabolism, vitamin B<sub>12</sub> concentration and flows, and nutrient degradability. We did not find an effect of Co source on pH (<i>P </i>= 0.92) or concentrations of acetate (<i>P </i>= 0.32), propionate (<i>P </i>= 0.15), butyrate (<i>P </i>= 0.92), and other VFA. However, we found that D-lactate concentration was greater in CoCO<sub>3</sub> than other treatments (<i>P </i>= 0.03), and total lactate was greater in CoCO<sub>3</sub> compared to CoAA and CoPec+CoAA (<i>P </i>= 0.04). Vitamin B<sub>12</sub> in liquid outflow tended to be lower with CoCO<sub>3</sub> (<i>P </i>= 0.10). Moreover, there was greater bacterial N flow (<i>P </i>= 0.01) and also greater N use efficiency (<i>P </i>= 0.01) in CoAA than CoCO<sub>3</sub> and CoPec. For nutrient degradation, we found a greater ruminal degradability of NDF (<i>P </i>< 0.01) in CoAA and CoPec+CoAA compared to CoCO<sub>3</sub> and CoPec. Our results indicate that, at a supplementation rate of 1 mg Co per kg diet DM, the tested Co sources affected fermentation of ruminal contents in continuous culture. Specifically, under the conditions of this experiment with dairy cattle diets, CoAA promoted greater microbial protein synthesis, NDF degradability, and liquid-associated vitamin B<sub>12</sub> flow compared to CoCO<sub>3</sub> and CoPec, suggesting enhanced Co utilization by ruminal microorganisms when CoAA is included as the primary Co source in the diet.

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Journal
Translational Animal Science
Published
2025-01-01
DOI
https://doi.org/10.1093/tas/txaf123
Citations
2
Primary Topic
Selenium in Biological Systems
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article
Field-Weighted Citation Impact
2.24
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article

Effects of novel organic sources of cobalt on ruminal fermentation, nutrient degradation and vitamin B12 synthesis in vitro

Charese A Hammond, José Arce, Kaliandra Souza Alves, A.P. Faciola et al.
2 citations
Translational Animal Science
Selenium in Biological Systems
2.24
article

Effects of novel organic sources of cobalt on ruminal fermentation, nutrient degradation and vitamin B12 synthesis in vitro

Charese A Hammond, José Arce, Kaliandra Souza Alves, A.P. Faciola, Richard Roberto Lobo, Efstathios Sarmikasoglou, Ana Carolina Silva Vicente, James R Vinyard, Mikayla L Johnson, Gerald K Salas-Solís, Szu-Wei Ma, Martha U Siregar, Michael T. Socha
article en
2 citations

Abstract

Cobalt (Co) is essential for vitamin B<sub>12</sub> synthesis in the rumen and energy metabolism in cattle. Previous studies on organic Co sources have shown variable effects on dairy cows' performance, focusing primarily on Co glucoheptonate as an alternative to the traditional Co carbonate (CoCO<sub>3</sub>). Our objective was to evaluate the effects of novel organic Co sources on ruminal microbial fermentation, nutrient degradation, and vitamin B<sub>12</sub> synthesis using a dual-flow continuous culture system. We used eight fermenters in a duplicated 4 × 4 Latin Square design, where each -fermenter was provided daily with 106 g DM of a basal diet plus the corresponding Co treatment. The treatments consisted of supplementing 1 mg Co/kg DM from the following Co sources: (i) CoCO<sub>3</sub>, (ii) Co Pectin (CoPec), (iii) Co Amino Acid (CoAA), and (iv) Co Pectin + Co Amino Acid (CoPec+CoAA). Data were analyzed with the MIXED procedure of SAS 9.4 to evaluate the effect of Co source on pH, VFA, N metabolism, vitamin B<sub>12</sub> concentration and flows, and nutrient degradability. We did not find an effect of Co source on pH (<i>P </i>= 0.92) or concentrations of acetate (<i>P </i>= 0.32), propionate (<i>P </i>= 0.15), butyrate (<i>P </i>= 0.92), and other VFA. However, we found that D-lactate concentration was greater in CoCO<sub>3</sub> than other treatments (<i>P </i>= 0.03), and total lactate was greater in CoCO<sub>3</sub> compared to CoAA and CoPec+CoAA (<i>P </i>= 0.04). Vitamin B<sub>12</sub> in liquid outflow tended to be lower with CoCO<sub>3</sub> (<i>P </i>= 0.10). Moreover, there was greater bacterial N flow (<i>P </i>= 0.01) and also greater N use efficiency (<i>P </i>= 0.01) in CoAA than CoCO<sub>3</sub> and CoPec. For nutrient degradation, we found a greater ruminal degradability of NDF (<i>P </i>< 0.01) in CoAA and CoPec+CoAA compared to CoCO<sub>3</sub> and CoPec. Our results indicate that, at a supplementation rate of 1 mg Co per kg diet DM, the tested Co sources affected fermentation of ruminal contents in continuous culture. Specifically, under the conditions of this experiment with dairy cattle diets, CoAA promoted greater microbial protein synthesis, NDF degradability, and liquid-associated vitamin B<sub>12</sub> flow compared to CoCO<sub>3</sub> and CoPec, suggesting enhanced Co utilization by ruminal microorganisms when CoAA is included as the primary Co source in the diet.

Translational Animal ScienceVol. 9
University of Alaska Fairbanks (US), Universidad de Costa Rica (CR), University of Florida (US), Zinpro (United States) (US), Michigan State University (US)
Openalex Percentile: Top 12%
Selenium in Biological Systems
2.24
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