Abstract
Minerals play an important role in animal metabolism. Knowledge of mineral requirements allows well-formulated diets to be provided, which is the main factor that affects performance. To determine the macromineral and trace element requirements for growth and maintenance, thirty-eight 2-month-old Santa Ines lambs with initial body weight (BW) of 13.0 ± 1.49 kg were distributed in a factorial design with feeding levels (ad libitum, 30% and 60% feed restriction) and sex classes [castrated (CM) and intact males (IM)]. The net mineral requirements for gain were higher (P < 0.05) with increasing BW and average daily gain, except for Ca and Na, which remained constant as the empty BW (EBW) increased. The macromineral net requirement for maintenance (g/kg EBW0.75) and the true retention coefficient (k; %) were 0.0784 and 65.2 for Ca, 0.0926 and 80.0 for P, and 0.0379 and 59.0 for K, respectively. The k of Mg was higher (P < 0.05) for IM (11.3 for IM and 7.9 for CM). Sex did not affect (P > 0.05) the maintenance requirement of the trace elements Co, Cu, Zn and Cr which were 0.0015, 0.037, 0.698, and 0.0055 (mg/kg EBW0.75), respectively. Our study indicated that the Santa Ines net mineral requirements are different from the main nutritional requirements established by committees for sheep, which may result in unbalanced diets.
Similar content being viewed by others
Introduction
The determination of mineral requirements of small ruminants is a key step to properly formulate and balance their diets, especially for animals in a growing phase. In Brazil, ruminant diets are formulated according to the recommendations proposed by the ARC1, NRC2,3, AFRC4, CSIRO5 and INRA6 committees. In general, the dataset of those committees is based on data obtained from trials using wool sheep. However, it is unknown whether the requirements of hair sheep in the tropics have been carefully considered, especially given their phenotypic differences, potential for weight gain, and body composition, which are known to affect the nutritional requirements of animals7.
Mineral requirements are generally based on supplementation3, which disregards the mineral composition of the feed. The mineral requirement knowledge has a global importance. Among the hair sheep breeds that are well adapted to environmental conditions in warm areas, Santa Ines sheep are a dominant breed for meat production. The amount of mineral retained in the animal's body in relation to that consumed is necessary to determine the need for macrominerals and trace elements for the maintenance and growth of the animals8 as well as to decrease unnecessary excretion of those minerals in the environment9.
The majority of feeding systems for sheep3,5,10 use the absorption coefficient of each mineral to calculate dietary requirements because they consider that the excretion of minerals through the urine is minimal1. The maintenance requirement for minerals is determined from the knowledge of the minerals retained in the animal's body in relation to the minerals consumed8. One of the advantages of using the retention coefficient is that it indicates the real relationship between consumed and retained minerals in the animal's body.
We hypothesized that the demand for minerals by Santa Ines hair sheep may be different from wool sheep due to the peculiarities of these animal. The objective of this study was to evaluate the body composition and the macromineral and trace element requirements for Santa Ines sheep.
Methods
Local, animal studies and data statement
This study was conducted at the Animal Nutrition Laboratory of the Department of Animal Science of the Federal University of Ceara in Fortaleza, Ceara State, Brazil (30° 43′ 02″ S, 33° 32′ 35″ W). Animal experiments were conducted in accordance with the Guiding Principles for the Care and Use of Research Animals developed by the Federal University of Ceara, Fortaleza, Brazil. The protocol and methods were approved by the Ethics Committee on Animal Research of the Federal University of Ceara (No. 98/2015). Information provided in the manuscript complies with the essential recommendations for reporting of the ARRIVE guidelines.
Animals, diets, and experimental design
Thirty-eight 60-day-old Santa Ines hair lambs averaging 13.0 ± 1.49 kg body weight (BW) were allocated in individual stalls. The sheep were dewormed using 0.3 mL of ivermectin (Ivomec; Merial, Duluth, GA, USA), vaccinated for clostridiosis using 4 mL of polyvalent Clostridium vaccine per animal (Poli-star; Vallée, Montes Claros, Brazil), and later supplemented with 0.3 mL of vitamins ADE (Vit A, 20.000.000 IU; Vit D3, 5,000,000 IU; and Vit E, 6000 IU/100 mL; Vallée, Montes Claros, Brazil). Among the 38 sheep, 19 were chosen at random and subjected to castration using the Burdizzo method of castration. In brief, 2.5–5 mL of local anesthetic in 2% xylocaine was injected subcutaneously on each side of the spermatic cord, and the operation was performed after 5 min. The animals were submitted to an adaptive period of 15 days. Posteriorly, four lambs of each sex [4 castrated male (CM) and 4 intact male (IM) Santa Ines lambs] were randomly selected and slaughtered to serve as a baseline group (Table S1). Then, the remaining lambs (n = 30) were assigned to a completely randomized design with three feeding levels (ad libitum, 30% and 60% feed restriction) and two sexes (CM and IM) composing a 3 × 2 factorial scheme. The experimental rations were formulated to meet a gain of 200 g/day as recommended by the NRC3.
The lamb diet consisted of 600 g/kg hay and 400 g/kg concentrate (Table 1). Feed was offered as a total mixed ration (TMR) two times per day (at 08:00 and 16:00 h). The orts from the lambs in the ad libitum group were removed before each morning feeding and weighed to calculate the intake and feeding level of the lambs undergoing 30% and 60% feed restriction. Water was provided ad libitum for all animals. The animals were weighed every seven days to calculate body weight gain (BWG). All lambs were slaughtered when the lambs in the ad libitum group reached an average of 30 kg BW. Based on that criterion, the experimental trial lasted 100 days.
Slaughter procedures
Slaughter procedures were carried out in accordance with regulatory standards established by the Animal Care and Use Committee. Before slaughter, the animals were deprived of solid and liquid feed for 18 h. The animals were then stunned per a brain concussion and slaughtered by cutting the jugular vein. All non-carcass components (liver, heart, lungs, trachea, tongue, kidneys, spleen, hide, head, and feet) and the digestive tract (rumen, reticulum, omasum, abomasum, small intestines, and large intestines) were weighed, emptied, cleaned, and weighed again.
Blood was weighed and mixed with the other body parts to be further chemically analyzed. All body parts were weighed separately, frozen, ground, and mixed to be later chemically analyzed. Measurement of body mass was obtained by determining only the empty BW (EBW), which was obtained after the animal was slaughtered. The EBW was calculated as the difference between the BW at slaughter and the contents of the gastrointestinal tract and bladder.
Subsequently, the carcasses were refrigerated at 4 °C for 24 h. Posteriorly, the carcasses were divided in half (right and left carcasses). The right half-carcass and all non-carcass components were frozen, subsequently sawed with a band saw, and ground with an industrial cutter. After homogenization, 500 g of carcass and non-carcass components was sampled and stored in a freezer at − 20 °C.
Chemical analyses
For performing chemical analyses, 500 g of each sample of the organ mass, half-carcass mass of the ground organs, blood, hooves, head, and right half of the carcass and hide were dried in a forced-ventilation oven at 55 °C for 72 h. Posteriorly, the samples were defatted by extraction with ether in a Soxhlet apparatus (Association of Official Analytical Chemists (AOAC)11; method number 920.39) and then ground in a ball mill. Dry matter (DM) was determined by using the method 967.03 from the AOAC11. The ash (AOAC, 1990; method 942.05)11 and crude protein (AOAC, 1990; method 981.10)11 levels were determined from fat-free samples. The body water content was determined as 100% minus the DM.
Samples of feed, body, rations, and orts were evaluated for mineral composition through digestion in nitroperchloric acid, according to the INCT-CA M-004/1 method described by Detmann et al.12, thus obtaining a mineral solution from which dilutions were made to quantify the minerals. The Ca and Mg concentrations were determined by adding strontium chloride and using atomic absorption spectrometry (GBC Avanta Sigma, Hampshire, USA) (Method 968.08; AOAC)13. The Na and K concentrations were determined by flame emission spectrometry (Corning 400, NY, USA) (Method 985.35, AOAC)13. The P concentration was determined by reduction of the phosphorus-molybdate complex with ascorbic acid followed by measurement using a colorimetric spectrophotometer (Method 965.17, AOAC)13. The Co, Cu, Mn, Zn, and Cr concentrations were determined by spectrometry (GBC Avanta Sigma, Hampshire, USA) (Method 968.08; AOAC)13.
Models and calculations
The retained mineral content was determined by the difference in the amount of minerals in the initial EBW (reference animals) and final EBW (experimental animals).
The model of Lofgreen and Garrett14 was used to estimate the net requirements for maintenance according to the following equation:
where RM is the retained mineral (mg kg EBW0.75 day); MI is the mineral intake (mg kg EBW0.75 day); a is the maintenance requirements; and b is the retention coefficient.
The model of Brody15 was used to estimate the body composition of minerals in the EBW as follows:
where BCM is the body content of the mineral (g); and ‘a’ and ‘b’ are regression parameters.
The net requirements of the minerals for gain were estimated by deriving Eq. (2) as follows:
where NMg is net requirement for weight gain (g/day); ‘a’ and ‘b’ are parameters of the equation; and EBW is expressed in kilograms.
The requirements based on the EBW were converted to the BW using 1.18, a factor of conversion derived from the relationship between BW and EBW.
Statistical analyses
Significance of treatments was verified by a two-way ANOVA model as follows: Yij = μ + Si + Rj + (SR)ij + eij; where Yij is the response variable, i.e., body composition parameters; Si the effect of sex (CM or IM); Rij is the feed restriction (ad libitum, 30% and 60% feed restriction); (SR)ij is the interaction of feed restriction by sex; and eij is the term for residuals.
Net requirements for maintenance and true retention coefficient were estimated using Eq. (1) through mixed models and testing sexual class effects using Eqs. (1) and (2). If parameters differed from zero, a variance component structure for the (co)variance matrix was used to fit equations. The Gauss–Newton method was used to solve nonlinear models for growth, and a P-value threshold of 0.05 was adopted to consider parameter differences. Influential records were not used when studentized residuals were greater than an absolute value of two.
All analyses were performed by SAS software (SAS Inst. Inc., Cary, NC) using the GLM procedure with a level of significance equal to 0.05 for two-way ANOVA and NLIN for nonlinear models.
Results
Dry matter (DM) intake, mineral intake, and body parameters
The DM and mineral intake decreased with increasing dietary restriction (P < 0.05; Table 2), but there was no sex effect (P > 0.05). The Na content in the EBW was higher in animals with 60% feed restriction (P = 0.001) than in the other animals.
The Mg (0.56 vs. 0.68), Na (1.41 vs. 1.59), Co (1.49 vs. 1.64), and Mn (1.18 vs. 1.40) concentrations were higher (P < 0.05) to CM than IM whereas the other minerals were similar between the sexes (Table 3). The equations for estimating body composition and net gain requirements are shown in Table 4.
Net mineral and trace element requirements
Sex affected (P < 0.05) the concentrations of Mg, Mn, and Cr in the empty BW gain (EBWG; Table 4). The net mineral requirements for gain were higher (P < 0.05) with increasing BW and average daily gain (ADG), except for Ca and Na, which remained constant as the EBW increased (Table 5).
The net requirements of Mg and Mn for gain were 35% higher for CM than for IM with 30 kg BW and an ADG of 200 g (Tables 5, 6). The dietary requirements of Mg and Mn were 50.8% and 29.3% higher, respectively, for IM than for CM.
The equations used to estimate the requirements of macrominerals and trace elements for maintenance are shown in Table 7. The macromineral net requirement for maintenance (g/kg EBW0.75) and the true retention coefficient (k; %) were 0.0784 and 65.2 for Ca, 0.0926 and 80.0 for P, and 0.0379 and 59.0 for K, respectively. The Mg requirement was similar between sexes (0.0065), but the true retention coefficient was different (11.3 for IM and 7.9 for CM). The Na maintenance requirement was different between the sexes (0.0242 vs. 0.0167 for IM and CM, respectively), but the k (84.3) was similar. Sex did not affect (P > 0.05) the maintenance requirement of the trace elements Co, Cu, Zn and Cr which were 0.0015, 0.037, 0.698, and 0.0055 (mg/kg EBW0.75), respectively.
Comparison of total dietary minerals requirements between the committees
The total dietary requirements of this study and those presented at the NRC3 and INRA6 committees are shown in Figs. 1 and 2. The dietary requirements with 30 kg BW and an ADG of 200 g for Cu (9.77 mg/day), Mn (69.11 mg/day for IM and 98.03 mg/day for CM), and Co (0.21 mg/day) were higher than those proposed by the NRC3, which recommended 5.53, 20.53 and 0.17 mg/day for Cu, Mn and Co, respectively. However, the requirements of Co and Cu were lower than those reported by the INRA6 committee, which recommended 0.31 and 15.54 mg/day, respectively. Besides, the Zn level (64.99 mg/day) was higher than the values recommended (51.83 mg/day) by the INRA6 committee.
Discussion
The NRC3, CSIRO5, and INRA6 international committees play an important role in nutritional recommendations for sheep, especially for those in the temperate region. In tropical scenarios, the nutritional requirements recommended by international committees may not be adequate to meet the physiological needs at different stages of animal life. Factors such as mathematical, environmental conditions3, genotype16, body composition, sex, and feed quality7 may influence the mineral requirements. In our study, the higher DM and mineral intake in sheep fed ad libitum resulted in greater performance (final BW, EBW, and ADG), indicating that the animals’ response was directly influenced by the level of intake. The DM intake is an important variable affecting animal performance because it guarantees the organism adequate nutrients and energy substrates for biochemical reactions to meet maintenance requirements. The 60% feed restriction was sufficient to meet the animals’ essential survival processes. Factors such as age, sex class, and genetic group influence nutritional requirements5.
The Ca is the most abundant mineral element in the animal body6, and approximately 98% percent of Ca in the body is located within the skeleton where it, along with phosphate anions, serves to provide structural strength and hardness to bone. Thus, lambs with a BW of 10 to 30 kg had decreased Ca concentration (% of EBW) and consequently net requirements of Ca. When compared to the committee’s recommendation for lambs weighing 20 kg and fed for an ADG of 200 g/day, the lambs had similar Ca requirements to those suggested by the NRC3. The mineral body composition oscillates according to the animal age and nutritional status. The bone tissue proportion will decrease because the largest amount of Ca and P in the body is in the bones17. Later, with the progression of growth, there is an increase in the proportion of fat followed by a reduction in the proportions of water, protein, and minerals in the body, particularly after 30 kg of BW. This pattern of nutrient deposition in the body is directly related to the stages of development of the bone, muscle, and adipose tissues18. Nevertheless, evaluating chemical constituents of Brazilian Somalis, in the same range of BW, there was a decrease in ash content in the animal's body, which leads to a reduction in Ca requirements9.
In the present study, the Na concentration remained constant as the BW increased (10 to 30 kg of BW). Most of the Na present in the animal body is located in the soft tissues and body fluids. A decrease in the water amount in the BW of the animals during this growth period was observed, which, in turn, consequently decreased the Na concentration in their bodies.
The sexual class is one of the factors that influence the chemical constituents of the animal's body19,20. However, the NRC3 and CSIRO5 have not provided inferences about the sex influence on mineral requirements. Differences in the requirements for Mg, Mn, and Cr were observed for Santa Ines males during the evaluated growth phase. Mg is closely associated with Ca and P. Approximately 70% of Mg in the total body is present in the skeleton. The Mg is an enzyme activator, including enzymes involved in the transfer of phosphate21. The CM have higher requirements for Mg, possibly due to the higher fat content in the body. Increases in the requirements of Mg and Cr for gain are directly related to the energy expenditure of lipogenesis.
Recent studies have shown that Cr affects carbohydrate and/or lipid metabolism22,23. The higher Cr gain net requirements for CM (0.84 mg/day vs. 0.62 mg/day for CM and IM, respectively) suggested that Cr in CM might be more active to increase glucose levels for muscle and adipose tissue. It is well established that Cr supplementation increases insulin responsiveness24, mainly in non-ruminants. The Cr is an element that stimulates lipogenesis and inhibits lipolysis.
The recommendations of different committees consider their calculations of endogenous losses from feces. The maintenance requirement for minerals involves not only urinary and fecal losses that occur, but also those that may occur by skin, sweat, and among others. Concerning the mineral retention coefficients, the values were lower for Mg, Na, and K, which may be related to the high amount of these minerals in the diet and consequently increased excretion. Thus, despite an improvement in the estimates, the retention coefficients found in this study were not definitive and may change as a function of tissue growth25,26. Animals at the beginning of life tend to have higher retention coefficients than adult animals. Therefore, the degree of variation in retention/absorption coefficients according to growth function is yet to be determined.
In our study, the Ca concentration (0.78 g/day) for the maintenance of hair sheep with a BW of 30 kg were lower than those recommended by the NRC and INRA (0.94 and 0.99 g/day, respectively). However, the P concentrations (0.98 g/day) for the maintenance were higher than the recommended by the NRC (0.73 g/day) and lower than the recommended by INRA (1.30 g/day). The requirement of Mg (0.03 g/day) was lower than those recommended by the NRC3 (0.09 g/day) and INRA6 (0.42 g/day). For Na, the maintenance requirements were 0.10 g/day for CM and 0.16 g/day for IM. These values were lower than those proposed by the NRC3 (0.32 g/day) and INRA6 (0.45 g/day). For K, the maintenance requirement was 0.30 g/day, which was lower than those suggested by the NRC3 (4.10 g/day) and INRA6 (3.15 g/day).
Trace elements, especially those more recently discovered, are required for maintaining the health and performance of farm animals27,28. Because these elements are either required in low concentrations or are commonly distributed in animal diets, deficiencies are likely to be exceptional under normal practical conditions.
Interestingly, this study demonstrated that sex affects the Mg and Mn requirements of males. Additionally, the results indicated that mineral requirements for weight gain and maintenance in Santa Ines sheep are different than those suggested by the global sheep feeding systems. It is essential for nutritionists and government regulators to establish the requirements for each mineral to optimize animal health and minimize tissue residues.
References
Agricultural Research Council. The Nutrient Requirement of Ruminant Livestock (CABI, 1980).
National Research Council. Nutrient Requirements of Sheep (National Academies Press, 1985).
National Research Council. Nutrient Requirements of Small Ruminants: Sheep, Cervids and New World Camelids (National Academies Press, 2007).
Agricultural and Food Research Council. Technical committee on responses to nutrients, Report 6. A reappraisal of the calcium and phosphorus requirements of sheep and cattle, Report n. 6. Nutr. Abstr. Rev. 61, 576–612 (1991).
Commonwealth Scientific and Industrial Research Organization. Nutrient Requirements of Domesticated Ruminants (CSIRO Publishing, 2007).
Institut National de la Recherche Agronomique. INRA Feeding System for Ruminants (Wageningen Academic Publishers, 2018).
Pereira, E. S. et al. Net mineral requirements for the growth and maintenance of Somali lambs. Animal 13, 112–118 (2018).
Valadares Filho, S. C. et al. Nutrient Requirements of Zebu and Crossbreed Cattle- BR-CORTE 3rd edn. (Suprema Gráfica Ltda, 2016).
Pereira, E. S. et al. Energy and protein requirements of Santa Ines lambs, a breed of hair sheep. Animal 11, 2165–2174 (2017).
Institut National de la Recherche Agronomique. Alimentation des bovins, ovins et caprins. Besoins des animaux. Valeurs des aliments (Editions Quae, 2007).
Association of Official Analytical Chemist. Official Methods of Analysis (AOAC International, 1990).
Detmann, E. et al. Métodos para análise de alimentos (Suprema, 2012).
Association of Official Analytical Chemist. Official Methods of Analysis (AOAC International, 2000).
Lofgreen, G. P. & Garrett, W. N. A system for expressing net energy requirements and feed values for growing and finishing beef cattle. J. Anim. Sci. 27, 793–806 (1968).
Brody, S. Bioenergetics and Growth with Special Reference to the Efficiency Complex in Domestic Animals (Reinhold Publishing Corporation, 1945).
Teixeira, I. A. M. A. et al. Mineral requirements for growth of wool and hair lambs. R. Bras. Zootec. 42, 347–353 (2013).
Suttle, N. F. The Mineral Nutrition of Livestock (CABI, 2010).
Lawrence, T., Fowler, V. & Novakofski, J. Growth of Farm Animals (CABI, 2012).
Ahmed, M. M. M., Siham, A. K. & Barri, M. E. S. Macromineral profile in the plasma of Nubian goats as affected by the physiological state. Small Rumin. Res. 38, 249–254 (2000).
Herring, M. J., Oskui, P. M., Hale, S. L. & Kloner, R. A. Testosterone and the cardiovascular system: a comprehensive review of the basic science. J. Am. Heart. Assoc. 2, e000271 (2013).
Ammerman, C. B. & Goodrich, R. D. Advances in mineral nutrition in ruminants. J. Anim. Sci. 57, 519–533 (1983).
Gentry, L. R. et al. Dietary protein and chromium tripicolinate in Suffolk wether lambs: effects on production characteristics, metabolic and hormonal responses and immune status. J. Anim. Sci. 77, 1284–1294 (1999).
Summer, J. M., Valdez, F. & McNamara, J. P. Effects of chromium propionate on response to an intravenous glucose tolerance test in growing Holstein heifers. J. Dairy Sci. 90, 3467–3474 (2007).
Sano, H., Nakai, M., Kondo, T. & Terashima, Y. Insulin responsiveness to glucose and tissue responsiveness to insulin in lactating, pregnant, and nonpregnant, nonlactating beef cows. J. Anim. Sci. 69, 1122–1127 (1991).
Geraseev, L. C., Perez, J. R. O., Resende, K. T., Silva Filho, J. C. & Bonagurio, S. Composição corporal e exigências nutricionais em cálcio e fósforo para o ganho e mantença de cordeiros Santa Inês dos 25 aos 35 kg de peso vivo. Bol. Ind. Anim. 56, 75–84 (1999).
Castro, M. M. D. et al. Determination of macromineral requirements for preweaned dairy calves in tropical conditions. J. Dairy Sci. 102, 2974–2984 (2019).
Underwood, E. & Suttle, N. F. The Mineral Nutrition of Livestock (Commonwealth Agricultural Bureaux, 1999).
Frøslie, A. Problems on deficiency and excess of minerals in animal nutrition. In Geomedicine (ed. Lag, J.) 37–60 (CRC Press, 1990).
Acknowledgements
This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) under Project number 308145/2018-6 and for a scholarship from the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) to the first author.
Author information
Authors and Affiliations
Contributions
E.S.P. conceptualized the methodology; D.L.S. and F.W.R.L. performed the experiment and collected data; L.R.B. and R.L.O. analyzed the data; M.I.M., J.P.P.R. and L.P.S. performed the statistical analysis; E.S.P., C.J.L.H. and J.G.S. wrote the manuscript; E.S.P. supervised the project; E.S.P. administered the project; and E.S.P. acquired funding. All authors reviewed and agreed to the published version of the manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Sousa, D.L., Marcondes, M.I., Silva, L.P. et al. Macromineral and trace element requirements for Santa Ines sheep. Sci Rep 11, 12329 (2021). https://doi.org/10.1038/s41598-021-91406-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-021-91406-w
- Springer Nature Limited