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Review

Cobalt and Vitamin B12 in Dairy Cattle Nutrition: Requirements, Functions, and Interactions

Department of Animal Sciences, University of Florida, Gainesville, FL 32608, USA
*
Author to whom correspondence should be addressed.
Animals 2025, 15(23), 3477; https://doi.org/10.3390/ani15233477 (registering DOI)
Submission received: 8 October 2025 / Revised: 8 November 2025 / Accepted: 18 November 2025 / Published: 2 December 2025
(This article belongs to the Section Animal Nutrition)

Simple Summary

Minerals are vital nutrients in dairy cattle diets because they support growth, health, reproduction, and milk production. Among these, cobalt is especially important because it allows rumen microorganisms to make vitamin B12, a vitamin that cows cannot produce on their own. Vitamin B12 is needed for energy production, glucose formation, and protein metabolism. When cows do not receive enough cobalt, vitamin B12 synthesis decreases, leading to poor growth, reduced appetite, lower milk yield, and health problems. Although only a small fraction of dietary cobalt is converted into vitamin B12, ensuring adequate supply is critical. The most recent guidelines recommend 0.2 mg cobalt per kg of diet dry matter (DM). This review summarizes the role of cobalt in ruminant nutrition, how diet composition and the rumen microbiome affect vitamin B12 synthesis, and how cobalt supplementation supports animal performance. Understanding these interactions can help improve mineral nutrition strategies and promote the health and productivity of dairy cattle.

Abstract

Minerals are essential for ruminant health, productivity, and metabolic function, with trace minerals playing critical roles at narrow dietary margins. Cobalt (Co) is essential as it supports ruminal microbial synthesis of vitamin B12 (cobalamin), which acts as a crucial cofactor in energy and protein metabolism. This review summarizes the role of cobalt in dairy cattle nutrition, emphasizing its contribution to vitamin B12 synthesis, propionate metabolism, and milk production. Only 3–15% of dietary cobalt is converted to vitamin B12, and efficiency depends on dietary composition, forage-to-concentrate ratio, and ruminal microbiome. Deficiency leads to reduced intake, poor growth, anemia, reproductive failure, and decreased milk yield. Cow’s milk contains ~0.5 µg/L of vitamin B12, with greater concentrations in colostrum; diet composition, supplementation, and genetics contribute to variability. Current recommendations set the cobalt requirement at 0.2 mg/kg diet DM, yet multiple environmental and nutritional factors can restrict vitamin B12 synthesis. Limitations of this review include heterogeneity among the studies reviewed, such as differences in trial design, animal genetics, diet composition, and environmental conditions, which may introduce variability and affect the generalizability and consistency of the findings. Collectively, findings highlight cobalt’s pivotal role in supporting microbial activity, energy metabolism, and production outcomes in dairy cows.

1. Introduction

Minerals are essential nutrients in ruminant diets because they support growth, health, reproduction, and productivity. They function in bone development, enzyme activity, electrolyte balance, blood clotting, and immune responses [1]. Ruminant minerals are classified into macrominerals and trace minerals, based on the dietary concentration required to meet nutritional needs.
Among trace minerals, cobalt is indispensable because it supports ruminal microbial synthesis of vitamin B12 (cobalamin). Ruminants cannot produce this vitamin themselves, making cobalt supply critical. Vitamin B12 functions as a cofactor for two enzymes: methionine synthase, which catalyzes the conversion of homocysteine to methionine in amino acid metabolism, and methylmalonyl–CoA mutase, which contributes to the catabolism of specific fatty acids and amino acids. Adequate vitamin B12 also supports ruminal propionate production, which the liver converts to glucose, a major precursor for lactose synthesis and milk production in dairy cows [2].
The most recent NASEM guidelines [3] doubled the estimated cobalt requirement to 0.2 mg/kg of dietary DM. However, the cobalt concentration of forages and many feedstuffs is typically insufficient to meet microbial and animal needs, making supplementation necessary [4]. Common supplemental sources include cobalt carbonate, cobalt sulfate, cobalt chloride, and cobalt glucoheptonate, whereas cobaltous oxide is not recommended because of poor bioavailability [2,5]. In addition, some studies found that cobalt supplementation increases vitamin B12 in dairy cows [6], but other studies did not observe this effect. This variability is likely due to differences in study design, animal genetics, diet composition, and environmental factors. The objective of this review is to identify current knowledge gaps regarding vitamin B12 metabolism in dairy cows, and to provide a comprehensive synthesis of recent findings to guide future research and nutritional strategies. This review summarizes the role of cobalt in ruminant nutrition, with an emphasis on cobalt’s importance for vitamin B12 synthesis, its contribution to nutrient metabolism, and its effects on production outcomes in dairy cattle. Studies were included based on their relevance to cobalt and vitamin B12 metabolism in dairy cows; only peer-reviewed articles and reviews published in English were considered, while non-peer-reviewed sources, conference abstracts, and studies unrelated to dairy cattle were excluded.

2. Minerals for Ruminants

Minerals are essential nutrients in dairy cattle diets and are classified according to the concentration required by the animal. Macrominerals are required at percent levels of dietary dry matter, whereas trace minerals are required at parts per million (ppm) [5]. Essential macrominerals include calcium (Ca), phosphorus (P), magnesium (Mg), sulfur (S), sodium (Na), chloride (Cl), and potassium (K) [5]. These minerals have critical physiological roles, and supplementation is required when forages or rations are deficient. Failure to meet requirements can result in metabolic disorders or, at excessive concentrations, toxicity.
Trace minerals essential for dairy cattle include cobalt (Co), copper (Cu), iodine (I), manganese (Mn), selenium (Se), and zinc (Zn). Each contributes to key physiological processes, and both deficiency and excess can impair metabolic function. Deficiencies in dairy cattle are frequently linked to imbalances in trace-mineral supply. Maintaining trace-minerals within narrow optimal ranges is necessary to support growth, enzyme activity, cellular metabolism, and immune function [5,7,8]. Given the wide range of physiological roles and the narrow margin between deficiency and excess, a clear overview of essential minerals and their functions is valuable. Table 1 and Table 2 summarize the major macrominerals and trace minerals required by dairy cattle, highlighting their key physiological functions and the typical deficiency symptoms observed when dietary supply is inadequate.

3. Cobalt and Vitamin B12

Cobalt (Co) is an essential trace-mineral required in small concentrations, approximately 0.1 to 0.2 mg per kg of dry matter [3]. In ruminants, it is a vital as it facilitates the microbial production of vitamin B12 within the rumen [4]. Its importance was first identified in 1935 when it was discovered that cobalt supplementation could remedy a condition marked by loss of appetite and weight decline in ruminants [8]. A few years later, in 1948, it was found that cobalt was an essential component of vitamin B12 for sheep and cattle, and its lack caused conditions such as coastal disease (in sheep), wasting disease or enzootic marasmus in cattle [8]. Animals suffering from this deficiency commonly exhibit non-specific symptoms, including lower feed consumption, slowed growth, muscle wasting, coarse fur, and thickened skin. They also frequently had reproductive issues and a decline in milk production [9].
Ruminal microorganisms are not highly efficient at converting dietary cobalt (Co) into vitamin B12, with only about 3–13% of ingested cobalt being utilized for this process [10,11]. The production of cobalamin is influenced by factors such as dietary fiber and the overall intake of dry matter [12]. However, among all variables, the amount of cobalt in the diet remains the primary driver of vitamin B12 synthesis in the rumen [12,13]. If cobalt is lacking in the feed, the microorganisms’ ability to produce vitamin B12 drops sharply within just a few days [14]. Rumen microbiome engineering is an emerging research field focused on manipulating the ruminal microbial ecosystem to optimize fermentation processes and improve ruminant productivity. Techniques include dietary interventions, probiotic supplementation, and microbial community modulation to favor beneficial microorganisms involved in nutrient cycling and cobalamin production [15,16]. These interventions can aim to enhance the microbial synthesis of vitamin B12, improve feed efficiency, and reduce methane emissions, contributing to sustainable ruminant production [17]. Advances in metagenomics and microbial ecology have expanded our understanding of microbial interactions and pathways critical to rumen function, informing targeted strategies for microbiome engineering [15]. However, variability in host genetics, diet, and environment presents challenges for consistent outcomes, indicating the need for further research to develop precise and effective microbiome management approaches.
Efficient energy metabolism in ruminants depends on vitamin B12, which is synthesized by rumen microorganisms during fermentation, provided dietary cobalt is sufficient (above 0.5 mg/mL in ruminal fluid) [18]. If cobalt levels fall below this threshold, vitamin B12 synthesis is impaired, reducing its availability to the animal [8,12].
Ruminal microorganisms synthesize vitamin B12, but production may decrease with abrupt dietary changes or stress, and cobalt deficiency impairs absorption. Adequate dietary cobalt allows microorganisms to meet the vitamin B12 needs of the cow, supporting microbial growth and propionate metabolism essential for glucose production [2,7].
Vitamin B12 acts as a growth factor for ruminal microorganisms and is crucial for propionate production, a key precursor for glucose in ruminants [19,20]. Severe vitamin B12 deficiency impairs propionate utilization [21]. In microorganisms, vitamin B12 serves as a cofactor for enzymes like methylmalonyl-CoA mutase, involved in glucose formation, and tetrahydrofolate methyltransferase, which plays a role in methionine synthesis and methyl group transfer [7].
Ruminal microbial synthesis of vitamin B12 is influenced by several factors, including dietary cobalt levels, diet composition, and rumen microbial populations [13,22]. Dietary cobalt is essential for microbial synthesis of vitamin B12, with greater fiber diets promoting greater production compared to high-starch diets [23].
Ruminal microorganisms play a key role in vitamin B12 synthesis, though only a few specialized bacterial species actually produce it [24,25]. Studies have shown that species like Selenomonas ruminantium and Megasphaera elsdenii produce the greatest amounts of vitamin B12 [24,26]. A high ruminal vitamin B12 concentration correlates with greater abundance of Prevotella, while lower vitamin B12 levels associate with higher levels of Bacteroidetes, Ruminiclostridium, and Butyrivibrio [25]. This suggests that the composition of the rumen microbiome significantly influences vitamin B12 levels.
To better illustrate the relationship between cobalt and vitamin B12 in ruminants, Table 3 summarizes the key aspects, including requirements, functions, efficiency of utilization, deficiency symptoms, dietary and microbiome effects, and metabolic roles. This synthesis highlights cobalt’s central role in microbial vitamin B12 synthesis and its downstream effects on energy metabolism, growth, and production responses in dairy cattle.

4. Vitamin B12 Bioavailability

Particle size, chelation, and source type all affect the bioavailability of vitamin B12 in ruminants. In contrast to inorganic forms like cobalt carbonate, which have poorer solubility and ruminal utilization, organic sources of cobalt, such as cobalt acetate and cobalt lactate, often have higher water solubility and bioavailability [2,18]. We have found that organic sources of Cobalt, when compared to CoCO3, improve vitamin B12 synthesis [31]. Chelated mineral forms improve microbial access for effective vitamin B12 production by shielding cobalt from early interactions in the rumen. Particle size also affects the rate of dissolution; smaller particles have more surface area and are more bioavailable. Research on various cobalt sources and forms is still scarce, though, and results can vary based on animal characteristics, microbial populations, and diet composition [32,33].

5. Vitamin B12 in Milk

Cow’s milk contains approximately 0.5 µg/L of vitamin B12, while in colostrum, vitamin B12 concentration is 4 to 10 times greater than milk [29]. It has been shown that the composition and management of the diet in dairy herds can affect the concentration of vitamin B12 in milk, mainly because the ruminal synthesis of vitamin B12 is affected by the diet [30,34].
Genetic factors may partially account for the variability in vitamin B12 concentrations observed among cows [35]. Additionally, dietary supplementation with folic acid and vitamin B12, either individually or in combination, can alter folate and vitamin B12 concentrations in milk [36].
Ruminal microorganisms require cobalt and certain dietary conditions to efficiently synthesize vitamin B12, which is essential for the cow’s energy and protein metabolism [37]. Diets high in forage and fiber promote greater vitamin B12 production compared to high-starch diets, and the rumen microbiome composition also significantly influences vitamin B12 synthesis and its levels in the cow’s blood and milk [11]. Legumes such as alfalfa and clover serve as natural sources of dietary cobalt for ruminants in some regions [38].
To better illustrate the factors that affect vitamin B12 levels in milk, Table 4 summarizes key findings from previous studies. This table highlights the baseline differences between milk and colostrum, the role of diet composition and forage-to-concentrate ratio, as well as the effects of supplementation and genetic variability. Collectively, these factors demonstrate that both nutrition and genetics play roles in shaping vitamin B12 concentrations in milk and colostrum.

6. Cobalt Requirement in Dairy Cattle

Vitamin B12 requirements in ruminant diets are closely linked to cobalt needs, as cobalt is a component of the B12 molecule. Ruminal microorganisms require 0.07 to 0.11 mg cobalt per kg of feed for optimal function, or a dietary supply of 0.07 to 0.2 mg/kg [5,43].
However, the concentration of cobalt in the diet used for these processes is relatively low in cows, varying from 3% to 15% [12,13,44]. However, according to Girard et al. [18], only 4% of cobalt in the diet was used for the synthesis of vitamin B12.
Young ruminants, whose rumens are not yet fully functional, require vitamin B12 from their diet, such as from colostrum or milk, until their rumen matures around six to eight weeks of age [40]. Akins et al.,2013 reported that depending on weight and metabolic status, cattle need 1.2 to 2.4 mg of cobalt daily, with a dietary upper limit of 25 mg/kg dry matter [10]. Current recommendations specify cobalt requirements as 0.11 mg/kg dry matter because cobalt’s primary role is to support rumen microorganisms, whose cobalt needs vary with ruminal conditions [19,42].
Cobalt in the diet is absorbed as a cation and does not return to the rumen, rendering it unavailable to ruminal microorganisms. Most absorbed cobalt is excreted in urine, with smaller amounts lost in bile [32]. Recommended cobalt supplementation ranges from 0.11 to 0.35 mg/kg of feed dry matter, with a maximum safe level of 10 mg/kg; toxicity occurs at 30 mg/kg [35,41]. The NRC [7] recommends 0.11 mg/kg dry matter, supplying about 1.2 mg/day for dry cows and 2.4 mg/day for lactating cows, to maintain plasma vitamin B12 levels above 0.3 µg/L.
The recommended cobalt level in ruminant diets is about 0.2 mg/kg of dry matter, with supplementation typically ranging from 0.1 to 0.2 ppm [32]. However, adequate cobalt intake does not always guarantee sufficient vitamin B12 synthesis, as factors like season, feed cobalt content, grazing behavior, animal characteristics, diet composition, and soil contamination also influence vitamin B12 production and utilization [37,40,45].
The dietary requirements for cobalt and its role in vitamin B12 synthesis are highly interdependent. While only a small fraction of dietary cobalt is converted to vitamin B12, adequate supply is essential for optimal microbial activity and ruminant health. Table 5 summarizes the key aspects of cobalt utilization, daily requirements, supplementation ranges, and the factors that influence vitamin B12 synthesis efficiency.
While many studies demonstrate positive effects of cobalt or vitamin B12 supplementation on ruminant health and productivity, some research reports minimal or no significant responses; refs. [2,4,31] found that supplemental dietary cobalt did not significantly affect cobalt concentrations in milk, serum, or liver, nor improve metabolic status in dairy cows. Similarly, Tiffany et al. and Grace et al. [45,46] observed little improvement in growth performance or vitamin B12 status with cobalt supplementation in beef cattle. They reported inconsistent production responses in dairy cows to vitamin B12 supplementation, which were influenced by dietary and animal factors. More recently, Lopreiato et al. [47] found that maternal cobalt and folic acid supplementation combined with rumen-protected methionine had limited effects on offspring biomarkers. These mixed findings highlight the complexity of cobalt metabolism and vitamin B12 bioavailability in ruminants and emphasize the importance of considering dietary composition, animal genetics, and environmental factors when evaluating supplementation outcomes.
Table 5. Summary of Cobalt and Vitamin B12 requirements in ruminants.
Table 5. Summary of Cobalt and Vitamin B12 requirements in ruminants.
AspectDetails
Microbial requirement0.07–0.11 mg Co/kg feed DM for efficient ruminal function [48]
Efficiency of dietary Co useOnly 3–15% of dietary Co used for vitamin B12 synthesis; ~4% reported by Girard and Matte, 2005) [36]
Young ruminantsRequire dietary vitamin B12 directly until rumen is functional (6–8 weeks of age) [40]
Daily requirement1.2–2.4 mg/day depending on weight and metabolic status [10]
Recommended dietary level0.11–0.35 mg/kg DM [7]
Toxicity thresholdToxic at ≥30 mg/kg DM [27]
Requirement updatesSets requirement at 0.2 mg/kg DM, with 0.1–0.2 ppm supplementation adequate [3]
Factors influencing B12 synthesisSeason, forage type, concentrate/forage ratio, age, species, nutrient interactions, and soil contamination [40]
DM—Dry Matter, Co—Cobalt, NASEM—National Academies of Sciences, Engineering, and Medicine, NRC—National Research Council.

7. Conclusions

In conclusion, cobalt is an essential trace mineral for both ruminal microorganisms and ruminants. This is because cobalt is an essential component of vitamin B12 which is synthesized by ruminal microorganisms. Vitamin B12 is also an essential cofactor for optimizing energy metabolism in both ruminal microorganisms and ruminant animals. In ruminants, microbial utilization of cobalt for vitamin B12 synthesis is influenced by dietary cobalt levels, diet composition, and ruminal microbiome structure, affecting fermentation. The recommended cobalt supplementation is 0.2 mg/kg of dry matter, which enhances vitamin B12 synthesis and can improve ruminal fermentation and milk yield.

Author Contributions

Conceptualization: M.S. and G.S.-S.; funding acquisition: A.P.F.; investigation; M.S. and G.S.-S.; methodology: M.S., G.S.-S. and A.P.F.; resources: A.P.F.; project administration: A.P.F.; writing—original draft: M.S. and G.S.-S.; writing—review and editing. M.S., G.S.-S. and A.P.F. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

AI was used exclusively to enhance the clarity and coherence of the text. The authors used ChatGPT-4o (OpenAI, San Francisco, CA, USA) to assist with grammar correction, language refinement, and improvement of readability. The tool was not used to generate scientific content, and all sections of the manuscript were written, reviewed, and approved by the authors, who are fully responsible for its content.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. McGrath, J.; Duval, S.M.; Tamassia, L.F.M.; Kindermann, M.; Stemmler, R.T.; de Gouvea, V.N.; Acedo, T.S.; Immig, I.; Williams, S.N.; Celi, P. Nutritional strategies in ruminants: A lifetime approach. Res. Vet. Med. 2018, 116, 28–39. [Google Scholar] [CrossRef] [PubMed]
  2. Raths, R.; Rodriguez, B.; Holloway, J.W.; Waite, A.; Lawrence, T.; van de Ligt, J.L.G.; Purvis, H.; Doering-Resch, H.; Casper, D.P. Comparison of growth performance and tissue cobalt concentrations in beef cattle fed inorganic and organic cobalt sources. Transl. Anim. Sci. 2023, 7, txad120. [Google Scholar] [CrossRef]
  3. NASEM. Nutrient Requirements of Dairy Cattle, 8th ed.; National Academies Press: Washington, DC, USA, 2021. [Google Scholar]
  4. Girard, C.L.; Duplessis, M. The importance of B vitamins in enhanced precision nutrition of dairy cows: The case of folates and vitamin B12. Can. J. Anim. Sci. 2022, 102, 201–210. [Google Scholar] [CrossRef]
  5. McDowell, L.R. Vitamins in Animal and Human Nutrition, 2nd ed.; Wiley-Blackwell: Ames, IA, USA, 2012. [Google Scholar]
  6. Dryden, L.P.; Hartman, A.M. Variations in the amount and relative distribution of vitamin B12 and its analog in the bovine rumen. J. Dairy Sci. 1971, 54, 235–246. [Google Scholar] [CrossRef]
  7. NRC. Nutrient Requirements of Dairy Cattle, 7th ed.; National Academy Press: Washington, DC, USA, 2001. [Google Scholar]
  8. NRC. Nutrient Requirements of Beef Cattle, 7th ed.; National Academy Press: Washington, DC, USA, 1996. [Google Scholar]
  9. Underwood, E.J.; Suttle, N.F. The Mineral Nutrition of Livestock, 3rd ed.; CABI Publishing: Wallingford, UK, 2002. [Google Scholar]
  10. Akins, M.S.; Bertics, S.J.; Socha, M.T.; Shaver, R.D. Effects of cobalt supplementation and vitamin B12 injections on lactation performance and metabolism of Holstein dairy cows. J. Dairy Sci. 2013, 96, 1755–1768. [Google Scholar] [CrossRef]
  11. Miller, J.; Wentworth, J.; McCullough, M.E. Effects of Various Factors on Vitamin B12 Content of Cows’ Milk. J. Agric. Food Chem. 1966, 14, 218–221. [Google Scholar] [CrossRef]
  12. Stemme, K.; Lebzien, P.; Flachowsky, G.; Scholz, H. The influence of an increased cobalt supply on ruminal parameters and microbial vitamin B12 synthesis in the rumen of dairy cows. Arch. Anim. Nutr. 2008, 62, 207–218. [Google Scholar] [CrossRef]
  13. Stemme, K.; Meyer, U.; Flachowsky, G.; Scholz, H. The influence of an increased cobalt supply to dairy cows on the vitamin B12 status of their calves. J. Anim. Physiol. Anim. Nutr. 2006, 90, 173–176. [Google Scholar] [CrossRef]
  14. Goff, J.P. Determining the mineral requirement of dairy cattle. In Proceedings of the 11th Annual Florida Ruminant Nutrition Symposium, Gainesville, FL, USA, 13–14 January 2000; pp. 106–132. [Google Scholar]
  15. Belanche, A.; Belzecki, G.; Hernandez-Sanabria, E.; Martínez-Fernandez, G.; Ramos-Morales, E.; de la Fuente, G. Editorial: Unravelling the unknown of the rumen microbiome: Implications for animal health, productivity, and beyond. Front. Microbiol. 2025, 16, 1720795. [Google Scholar] [CrossRef]
  16. Wang, K.; Xiong, B.; Zhao, X. Could propionate formation be used to reduce enteric methane emission in ruminants? J. Dairy Sci. 2023, 855, 158867. [Google Scholar] [CrossRef]
  17. Lai, W.; Alberdi, A.; Leu, A.; de Leon, A.V.P.; Kobel, C.M.; Aho, V.T.E.; Roehe, R.; Pope, P.B.; Hvidsten, T.R. Metabolic capabilities of key rumen microbiota drive methane emissions in cattle. mSystems 2025, 10, e0060125. [Google Scholar] [CrossRef]
  18. Paterson, J.; Engle, T.E. Trace Mineral Nutrition in Beef Cattle; University of Tennessee: Knoxville, TN, USA, 2005; p. 22. Available online: https://www.researchgate.net/profile/Partha-Swain/post/Can-anybody-help-with-ruminant-nutrition-textbook/attachment/59d638cc79197b807799602b/AS%3A398973325070344%401472134061881/download/tracemineralproceedings.pdf (accessed on 17 November 2025).
  19. Goff, J.P. Pathophysiology of calcium and phosphorus disorders. Vet. Clin. N. Am. Food Anim. Pract. 2000, 16, 319–337. [Google Scholar] [CrossRef]
  20. Herdt, T.H.; Hoff, B. The use of blood analysis to evaluate trace mineral status in ruminant livestock. Vet. Clin. N. Am. Food Anim. Pract. 2011, 27, 255–283. [Google Scholar] [CrossRef]
  21. Tanner, R.S.; Wolfe, R.S. Nutritional requirements of methanomicrobium mobile. Appl. Environ. Microbiol. 1988, 54, 625–628. [Google Scholar] [CrossRef] [PubMed]
  22. González-Montaña, J.; Escalera-Valente, F.; Alonso, A.J.; Lomilos, J.M.; Robles, R.; Alonso, M.E. Relationship between Vitamin B12 and Cobalt Metabolism in Domestic Ruminant: An Update. Animals 2020, 10, 1855. [Google Scholar] [CrossRef] [PubMed]
  23. Girard, C.L.; Matte, J.J. Effects of Intramuscular Injections of Vitamin B12 on Lactation Performance of Dairy Cows Fed Dietary Supplements of Folic Acid and Rumen-Protected Methionine. J. Dairy Sci. 2005, 88, 671–676. [Google Scholar] [CrossRef]
  24. Brito, A.; Chiquette, J.; Stabler, S.P.; Allen, R.H.; Girard, C.L. Supplementing lactating dairy cows with a vitamin B12 precursor, 5, 6-dimethylbenzimidazole, increases the apparent ruminal synthesis of vitamin B12. Animal 2015, 9, 67–75. [Google Scholar] [CrossRef] [PubMed]
  25. Franco-Lopez, J.; Duplessis, M.; Bui, A.; Reymond, C.; Poisson, W.; Blais, L.; Chong, J.; Gervais, R.; Rico, D.E.; Cue, R.I. Correlations between the Composition of the Bovine Microbiota and Vitamin B12 Abundance. mSystems 2020, 5, e00107-20. [Google Scholar] [CrossRef]
  26. Martens, J.H.; Barg, H.; Warren, M.J.; Jahn, D. Microbial production of vitamin B12: Ruminant nutrition implications. Appl. Microbiol. Biotechnol. 2002, 58, 275–285. [Google Scholar] [CrossRef]
  27. Smith, S.E.; Loosli, J.K. Cobalt and Vitamin 12 in Ruminant Nutrition: A Review. J. Dairy Sci. 1957, 40, 1215–1227. [Google Scholar] [CrossRef]
  28. Paterson, J.E.; Macpherson, A. A Comparison of serum vitamin B12 and serum methylmalonic acid as diagnostic measures of cobalt status in cattle. Vet. Rec. 1990, 126, 329–332. [Google Scholar] [PubMed]
  29. Beaudet, V.; Gervais, R.; Graulet, B.; Nozière, P.; Doreau, M.; Fanchone, A.; Castagnino, D.D.S.; Girard, C.L. Effects of dietary nitrogen levels and carbohydrate sources on apparent ruminal synthesis of some B vitamins in dairy cows. J. Dairy Sci. 2016, 99, 2730–2739. [Google Scholar] [CrossRef] [PubMed]
  30. Degnan, P.H.; Taga, M.E.; Goodman, A.L. Vitamin B12 as a modulator of gut microbial ecology. Cell Metab. 2014, 20, 769–778. [Google Scholar] [CrossRef]
  31. Arce-Cordero, J.A.; Siregar, M.U.; Salas-Solis, G.K.; Silva Vicente, A.C.; Vinyard, J.R.; Sarmikasoglou, E.; Johnson, M.L.; Lobo, R.R.; Ma, S.W.; Hammond, C.; et al. Effects of novel organic sources of cobalt on ruminal fermentation, nutrient degradation and vitamin B12 synthesis in vitro. Transl. Anim. Sci. 2025, 9, txaf123. [Google Scholar] [CrossRef] [PubMed]
  32. McDowell, L.R. Minerals in Animal and Human Nutrition, 2nd ed.; Elsevier Science B.V.: Amsterdam, The Netherlands, 2003. [Google Scholar]
  33. Kawashima, T.; Henry, P.R.; Ammerman, C.B.; Littel, R.C.; Price, J. Bioavailability of cobalt sources for ruminants. 2. Estimation of the relative value of reagent-grade and feed-grade cobalt sources from tissue cobalt accumulation and vitamin B12 concentrations. Nutr. Res. 1997, 17, 957–974. [Google Scholar] [CrossRef]
  34. Gray, M.J.; Escalante-Semerena, J.C. The cobinamide amidohydrolase (cobyric acid-forming) CbiZ enzyme: A critical activity of the cobamide remodelling system of Rhodobacter sphaeroides. Mol. Microbiol. 2009, 74, 1198–1210. [Google Scholar] [CrossRef]
  35. Rutten, M.J.M.; Bouwman, A.C.; Sprong, R.C.; van Arendonk, J.A.M.; Visker, M.H.P.W. Genetic variation in vitamin B-12 content of bovine milk and its association with SNP along the bovine genome. PLoS ONE 2013, 8, e62382. [Google Scholar] [CrossRef]
  36. Girard, C.L.; Matte, J.J. Folic acid and vitamin B12 requirements of dairy cows: A concept to be revised. Livest. Prod. Sci. 2005, 98, 123–133. [Google Scholar] [CrossRef]
  37. Santschi, D.E.; Berthiaume, R.; Matte, J.J.; Mustafa, A.F.; Girard, C.L. Fate of supplementary B-vitamins in the gastrointestinal tract of dairy cows. J. Dairy Sci. 2005, 88, 2043–2054. [Google Scholar] [CrossRef]
  38. Duplessis, M.; Pellerin, D.; Robichaud, R.; Fadul, D.; Girard, C.L. Impact of diet management and composition on vitamin B12 concentration in milk of Holstein cows. Animal 2019, 13, 2101–2109. [Google Scholar] [CrossRef]
  39. Anthony, W.B.; Couch, J.R.; Rupel, I.W.; Henderson, M.B.; Brown, C. Vitamin B12 in Blood of Newborn and Colostrum-Fed Calves and in Colostrum and Normal Milk of Holstein and Jersey Cows. J. Dairy Sci. 1951, 34, 749–753. [Google Scholar] [CrossRef]
  40. Duplessis, M.; Pellerin, D.; Cue, R.I.; Girard, C.L. Factors affecting vitamin B12 concentration in milk of commercial dairy herds: An exploratory study. J. Dairy Sci. 2016, 99, 4886–4892. [Google Scholar] [CrossRef]
  41. Castagnino, D.S.; Kammes, K.L.; Allen, M.S.; Gervais, R.; Chouinard, P.Y.; Girard, C.L. High-concentrate diets based on forages harvested at different maturity stages affect ruminal synthesis of B vitamins in lactating dairy cows. Animal 2017, 11, 608–615. [Google Scholar] [CrossRef] [PubMed]
  42. Duplessis, M.; Lapierre, H.; Ouattara, B.; Bissonnette, N.; Pellerin, D.; Laforest, J.P.; Girard, C.L. Whole-body propionate and glucose metabolism of multiparous dairy cows receiving folic acid and vitamin B-12 supplements. J. Dairy Sci. 2017, 100, 8578–8589. [Google Scholar] [CrossRef] [PubMed]
  43. Mills, C.F.; Haresign, W. Cobalt deficiency and cobalt requirements of ruminants. Recent Adv. Anim. Nutr. 1981, 129–140. [Google Scholar]
  44. Strobel, H.J. Vitamin B12-dependent propionate production by the ruminal bacterium Prevotella ruminicola 23. Appl. Environ. Microbiol. 1992, 58, 2331–2333. [Google Scholar] [CrossRef]
  45. Grace, N.D.; Knowles, S.O. Lack of production response in grazing dairy cows supplemented with long-acting injectable vitamin B12. N. Z. Vet. J. 2012, 60, 95–99. [Google Scholar] [CrossRef]
  46. Tiffany, M.E.; Spears, J.W.; Horton, L.X. Influence of dietary cobalt source and concentration on performance, vitamin B12 status, and ruminai and plasma metabolites in growing and finishing steers. J. Anim. Sci. 2003, 81, 3151–3159. [Google Scholar] [CrossRef]
  47. Lopreiato, V.; Alharthi, A.S.; Liang, Y.; Elolimy, A.A.; Bucktrout, R.; Socha, M.T.; Trevisi, E.; Loor, J.J. Influence of cobalt source, folic acid, and rumen-protected methionine on performance, metabolism, and liver tissue one-carbon metabolism biomarkers in peripartal Holstein cows. Animals 2023, 13, 2107. [Google Scholar] [CrossRef]
  48. Spears, J.W. Overview of Mineral Nutrition in Cattle: The Dairy and Beef; NRC: Gainesville, FL, USA, 2002; pp. 113–1126. Available online: https://www.researchgate.net/profile/Jerry-Spears/publication/255593316_Overview_of_Mineral_Nutrition_in_Cattle_The_Dairy_and_Beef_NRC/links/54d3855b0cf25017918237ad/Overview-of-Mineral-Nutrition-in-Cattle-The-Dairy-and-Beef-NRC.pdf (accessed on 17 November 2025).
Table 1. Essential macrominerals for dairy cattle: physiological functions and deficiency symptoms.
Table 1. Essential macrominerals for dairy cattle: physiological functions and deficiency symptoms.
MineralPrimary Physiological FunctionsDeficiency Symptoms
Calcium (Ca)Bone and teeth formation; muscle contraction; blood clottingRickets; milk fever; reduced growth
Phosphorus (P)Bone and teeth formation; energy metabolism (ATP, phosphorylation)Poor fertility; reduced
appetite; rickets
Magnesium (Mg)Enzyme cofactor; nerve transmission; muscle functionGrass tetany; muscle
tremors
Sulfur (S)Component of sulfur-containing amino acids (methionine, cysteine); microbial protein synthesisReduced microbial protein synthesis; poor growth
Sodium (Na)Osmotic balance; nerve impulse transmissionReduced appetite; poor growth; pica
Chloride (Cl)Osmotic balance; gastric acid (HCl)
Formation
Alkalosis; poor growth
Potassium (K)Osmotic balance; acid–base regulation; muscle functionMuscle weakness; poor
appetite; reduced milk yield
ATP—Adenosine triphosphate, HCL—Hydrochloric acid.
Table 2. Essential trace minerals for dairy cattle: physiological functions and deficiency symptoms.
Table 2. Essential trace minerals for dairy cattle: physiological functions and deficiency symptoms.
MineralPrimary Physiological FunctionsDeficiency Symptoms
Cobalt (Co)Required for vitamin B12 synthesis by
ruminal microorganisms
Vitamin B12 deficiency;
anemia; reduced appetite
Copper (Cu)Enzyme cofactor; connective tissue and
hemoglobin synthesis
Anemia; depigmentation; poor reproduction
Iodine (I)Thyroid hormone synthesis; metabolic
Regulation
Goiter; reproductive failure
Manganese (Mn)Enzyme cofactor; bone formation;
reproductive function
Skeletal deformities; poor
reproduction
Selenium (Se)Component of glutathione peroxidase;
antioxidant defense
White muscle disease; retained placenta
Zinc (Zn)Enzyme cofactor; wound healing; immune functionParakeratosis; impaired wound healing; poor growth
Table 3. Relationship between Cobalt and Vitamin B12 in ruminants.
Table 3. Relationship between Cobalt and Vitamin B12 in ruminants.
AspectKey FindingsReferences
RequirementCobalt required in very small amounts (~0.2 mg/kg DM).
dietary supply often insufficient
[3,8,11]
FunctionEssential precursor for microbial synthesis of vitamin B12 (cobalamin) in the rumen [27]
EfficiencyConversion of dietary Co to
vitamin B12 is low (3–13% of the dietary cobalt intake)
[18,28]
Threshold for synthesisRuminal synthesis requires >0.5 mg/L Co in ruminal fluid [9,12,19]
Deficiency signsReduced intake, poor growth, muscle wasting, rough coat,
reduced milk yield, reproductive issues
[9,20]
Metabolic role of B12Cofactor for methylmalonyl-CoA mutase (gluconeogenesis via
propionate) and methionine
synthase (methyl transfer, protein metabolism)
[7,22]
Dietary effectsHigh-fiber diets increase vitamin B12 synthesis (up to 3× greater vs. high-starch diets); starch depresses synthesis [10,29]
Microbiome effectsOnly a few microorganisms synthesize B12: Selenomonas ruminantium, Megasphaera elsdenii, Butyrivibrio fibrisolvens; greater B12 linked to Prevotella [22,25,30]
DM—Dry Matter, Co—Cobalt.
Table 4. Factors affecting Vitamin B12 concentration in milk.
Table 4. Factors affecting Vitamin B12 concentration in milk.
FactorEffect on Vitamin B12 in MilkReference(s)
Baseline levelsMilk contains ~0.5 µg/L vitamin B12; colostrum 4–10× greater [39]
Diet compositionAffects ruminal synthesis → alters milk vitamin B12 [40,41]
GeneticsExplains part of cow-to-cow variability [35,40]
Folic acid and B12
supplementation
Increases folate and vitamin B12 concentrations in milk [42]
Forage/concentrate ratio60:40 diet → greater ruminal synthesis of active vitamin B12 than 40:60 [37]
Dietary fiberPositive correlation with milk vitamin B12 concentration [40]
Dietary crude proteinNegative correlation with milk vitamin B12 concentration [40]
Natural cobalt sourcesLegumes (alfalfa, clover) provide cobalt for rumen B12 synthesis [10]
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Siregar, M.; Salas-Solis, G.; Faciola, A.P. Cobalt and Vitamin B12 in Dairy Cattle Nutrition: Requirements, Functions, and Interactions. Animals 2025, 15, 3477. https://doi.org/10.3390/ani15233477

AMA Style

Siregar M, Salas-Solis G, Faciola AP. Cobalt and Vitamin B12 in Dairy Cattle Nutrition: Requirements, Functions, and Interactions. Animals. 2025; 15(23):3477. https://doi.org/10.3390/ani15233477

Chicago/Turabian Style

Siregar, Martha, Gerald Salas-Solis, and Antonio P. Faciola. 2025. "Cobalt and Vitamin B12 in Dairy Cattle Nutrition: Requirements, Functions, and Interactions" Animals 15, no. 23: 3477. https://doi.org/10.3390/ani15233477

APA Style

Siregar, M., Salas-Solis, G., & Faciola, A. P. (2025). Cobalt and Vitamin B12 in Dairy Cattle Nutrition: Requirements, Functions, and Interactions. Animals, 15(23), 3477. https://doi.org/10.3390/ani15233477

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