Abstract
The objective of the study was to evaluate the effects of trace mineral supplementation in sows during gestation and lactation on the performance and health status of sows and their offspring. Sows (n = 30; Landrace × Yorkshire; avg parity = 3.9) were randomly allocated into two dietary treatments. Sows received a basal diet supplemented with 12 mg/kg Cu, 30 mg/kg Fe, 90 mg/kg Zn, 70 mg/kg Mn, 0.30 mg/kg Se, and 1.5 mg/kg I from an inorganic trace mineral source (ITM) or a blend of hydroxychloride and organic trace mineral source (HOTM) from day 1 of gestation until the end of the lactation period at day 21. Compared to the ITM, the HOTM supplementation increased (P < 0.05) both litter birth weight and individual piglet birth weight. Although not statistically significant, HOTM tended to increase (P = 0.069) the level of lactose in colostrum. HOTM increased (P < 0.05) the concentration of Mn and Se in the colostrum, milk, and serum of sows and/or piglets. Notably, the Zn concentration in the serum of sows was higher in sows supplemented with ITM compared to HOTM. Moreover, HOTM increased (P < 0.05) the activities of GPX and SOD in gestating sows and piglets, as well as increased (P < 0.05) cytokines (IL-1β, TNF-α, and IL-10) in the serum of sows. The immunoglobulins (IgA, IgG, and IgM) also increased in sows and/or piglets at certain experimental time points. In conclusion, HOTM supplementation positively affected piglet development and improved the health status of sows and piglets potentially by regulating redox homeostasis and immunity.
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs12011-024-04300-7/MediaObjects/12011_2024_4300_Fig1_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs12011-024-04300-7/MediaObjects/12011_2024_4300_Fig2_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs12011-024-04300-7/MediaObjects/12011_2024_4300_Fig3_HTML.png)
Data Availability
The datasets used and/or analyzed during the current study are publicly available.
References
Björkman S, Kauffold J, Kaiser MØ (2022) Reproductive health of the sow during puerperium. Mol Reprod Dev 90(7):561–579. https://doi.org/10.1002/mrd.23642
Stevenson P (2023) Links between industrial livestock production, disease including zoonoses and antimicrobial resistance. Anim Res One Health 1(1):137–144. https://doi.org/10.1002/aro2.19
Miao JF, Adewole D, Liu SX, ** PP, Yang CB, Yin YL (2019) Tryptophan supplementation increases reproduction performance, milk yield, and milk composition in lactating sows and growth performance of their piglets. J Agric Food Chem 67(18):5096–5104. https://doi.org/10.1021/acs.jafc.9b00446
Koketsu Y, Tani S, Iida R (2017) Factors for improving reproductive performance of sows and herd productivity in commercial breeding herds. Porcine Health Manag. https://doi.org/10.1186/s40813-016-0049-7
Riddersholm KV, Bahnsen I, Bruun TS, de Knegt LV, Amdi C (2021) Identifying risk factors for low piglet birth weight, high within-litter variation and occurrence of intrauterine growth-restricted piglets in hyperprolific sows. Animals 11:9. https://doi.org/10.3390/ani11092731
Zhang X, Wu Y, Liu X, Lin X, Liu Y, Kang L et al (2023) Proinflammatory polarization of macrophages causes intestinal inflammation in low-birth-weight piglets and mice. J Nutr 153(6):1803–1815. https://doi.org/10.1016/j.tjnut.2023.04.016
Tan CQ, Ji YC, Zhao XC, **n ZQ, Li JY, Huang SB et al (2021) Effects of dietary supplementation of nucleotides from late gestation to lactation on the performance and oxidative stress status of sows and their offspring. Anim Nutr 7(1):111–118. https://doi.org/10.1016/j.aninu.2020.10.004
Berchieri-Ronchi CB, Kim SW, Zhao Y, Correa CR, Yeum KJ, Ferreira ALA (2011) Oxidative stress status of highly prolific sows during gestation and lactation. Animal 5(11):1774–1779. https://doi.org/10.1017/s1751731111000772
Dong ZL, Liu S, Deng QQ, Li GY, Tang YL, Wu X et al (2023) Role of iron in host-microbiota interaction and its effects on intestinal mucosal growth and immune plasticity in a piglet model. Sci China Life Sci 66(9):2086–2098. https://doi.org/10.1007/s11427-022-2409-0
Wang D, Kuang Y, Lv Q, **e W, Xu X, Zhu H et al (2023) Selenium-enriched Cardamine violifolia protects against sepsis-induced intestinal injury by regulating mitochondrial fusion in weaned pigs. Sci China Life Sci 66(9):2099–2111. https://doi.org/10.1007/s11427-022-2274-7
Hostetler CE, Kincaid RL, Mirando MA (2003) The role of essential trace elements in embryonic and fetal development in livestock. Vet J 166(2):125–139. https://doi.org/10.1016/s1090-0233(02)00310-6
Daniel JB, Brugger D, van der Drift S, van der Merwe D, Kendall N, Windisch W et al (2023) Zinc, copper, and manganese homeostasis and potential trace metal accumulation in dairy cows: longitudinal study from late lactation to subsequent mid-lactation. J Nutr 153(4):1008–1018. https://doi.org/10.1016/j.tjnut.2023.02.022
Aplin JD, Myers JE, Timms K, Westwood M (2020) Tracking placental development in health and disease. Nat Rev Endocrinol 16(9):479–494. https://doi.org/10.1038/s41574-020-0372-6
Karkoodi K, Chamani M, Beheshti M, Mirghaffari SS, Azarfar A (2012) Effect of organic zinc, manganese, copper, and selenium chelates on colostrum production and reproductive and lameness indices in adequately supplemented Holstein cows. Biol Trace Elem Res 146(1):42–46. https://doi.org/10.1007/s12011-011-9216-5
Liu X, Adamo AM, Oteiza PI (2023) Marginal zinc deficiency during gestation and lactation in rats affects oligodendrogenesis, motor performance, and behavior in the offspring. J Nutr 153(10):2778–2796. https://doi.org/10.1016/j.tjnut.2023.08.029
NRC (2012) Nutrient requirements of swine, 12th edn. National Academies Press, Washington(DC)
Villagómez-Estrada S, Pérez JF, van Kuijk S et al (2021) Strategies of inorganic and organic trace mineral supplementation in gestating hyperprolific sow diets: effects on the offspring performance and fetal programming. J Anim Sci 99:7. https://doi.org/10.1093/jas/skab178
Liu Z, Bryant MM, Roland DA (2005) Layer performance and phytase retention as influenced by copper sulfate pentahydrate and tribasic copper chloride. J Appl Poult Res 14(3):499–505. https://doi.org/10.1093/japr/14.3.499
Luo XG, Ji F, Lin YX, Steward FA, Lu L, Liu B, Yu SX (2005) Effects of dietary supplementation with copper sulfate or tribasic copper chloride on broiler performance, relative copper bioavailability, and oxidation stability of vitamin E in feed. Poult Sci 84(6):888–893. https://doi.org/10.1093/ps/84.6.888
Shaeffer GL, Lloyd KE, Spears JW (2017) Bioavailability of zinc hydroxychloride relative to zinc sulfate in growing cattle fed a corn-cottonseed hull-based diet. Anim Feed Sci Technol 232:1–5. https://doi.org/10.1016/j.anifeedsci.2017.07.013
Zhang B, Guo Y (2007) Beneficial effects of tetrabasic zinc chloride for weanling piglets and the bioavailability of zinc in tetrabasic form relative to ZnO. Anim Feed Sci Technol 135(1–2):75–85. https://doi.org/10.1016/j.anifeedsci.2006.06.006
Guo YM, Ai HS, Ren J, Wang GJ, Wen Y, Mao HR et al (2009) A whole genome scan for quantitative trait loci for leg weakness and its related traits in a large F intercross population between White Duroc and Erhualian. J Anim Sci 87(5):1569–1575. https://doi.org/10.2527/jas.2008-1191
Herve L, Quesnel H, Greuter A, Hugonin L, Merlot E, Le Floc'h N (2023) Effect of the supplementation with a combination of plant extracts on sow and piglet performance and physiology during lactation and around weaning. J Anim Sci 101:skad282. https://doi.org/10.1093/jas/skad282
Liu M, Zhang L, Mo Y, Li J, Yang J, Wang J et al (2023) Ferroptosis is involved in deoxynivalenol-induced intestinal damage in pigs. J Anim Sci Biotechnol 14:1. https://doi.org/10.1186/s40104-023-00841-4
Deng J, Yang JC, Feng Y, Xu Z, Kuca K, Liu M, Sun LH (2024) AP-1 and SP1 trans-activated the expression of CYP1A1 and CYP2A6 in the bioactivation of AFB1 in chicken. Sci China Life Sci. https://doi.org/10.1007/s11427-023-2512-6
Deng ZC, Wang J, Wang J, Yan YQ, Huang YX, Chen CQ, Sun LH, Liu M (2024) Tannic acid extracted from gallnut improves intestinal health with regulation of redox homeostasis and gut microbiota of weaned piglets. Anim Res One Health 2(1):16–27. https://doi.org/10.1002/aro2.51
Yang JC, Huang YX, Sun H, Liu M, Zhao L, Sun LH (2023) Selenium deficiency dysregulates one-carbon metabolism in nutritional muscular dystrophy of chicks. J Nutr 153(1):47–55. https://doi.org/10.1016/j.tjnut.2022.12.001
Deng ZC, Yang JC, Huang YX, Zhao L, Zheng J, Xu QB, Guan L, Sun LH (2023) Translocation of gut microbes to epididymal white adipose tissue drives lipid metabolism disorder under heat stress. Sci China Life Sci 66(12):2877–2895. https://doi.org/10.1007/s11427-022-2320-y
Yan YQ, Liu M, Xu ZJ, Xu ZJ, Huang YX, Li XM, Chen CJ, Zuo G, Yang JC, Lei XG, Sun LH (2024) Optimum doses and forms of selenium maintaining reproductive health via regulating homeostasis of gut microbiota and testicular redox, inflammation, cell proliferation, and apoptosis in roosters. J Nutr 154(2):369–380. https://doi.org/10.1016/j.tjnut.2023.12.021
Acda SP, Chae J (2002) Effects of organic trace mineral supplementation on sows’ reproductive and neonates’ growth performance through 2 wk postweaning. Asian-Aust J Animal Sci 15(9):1312–1318. https://doi.org/10.5713/ajas.2002.1312
Ma L, He J, Lu X, Qiu J, Hou C, Liu B, Lin G, Yu D (2020) Effects of low-dose organic trace minerals on performance, mineral status, and fecal mineral excretion of sows. Asian-Australas J Anim Sci 33(1):132–138. https://doi.org/10.5713/ajas.18.0861
Wang S, Wu S, Zhang Y, Chen J, Zhou X (2022) Effects of different levels of organic trace minerals on oxidative status and intestinal function in weanling piglets. Biol Trace Elem Res 201(2):720–727. https://doi.org/10.1007/s12011-022-03174-x
Wan D, Yin Y (2023) Trace elements in nutrition and health: a deep dive into essentiality and mechanism of their biological roles. Sci China Life Sci 66(9):1949–1951. https://doi.org/10.1007/s11427-023-2426-3
Byrne L, Murphy RA (2022) Relative bioavailability of trace minerals in production animal nutrition: a review. Animals 12:15. https://doi.org/10.3390/ani12151981
Xu ZJ, Liu M, Niu QJ, Huang YX, Zhao L, Lei XG et al (2023) Both selenium deficiency and excess impair male reproductive system via inducing oxidative stress-activated PI3K/AKT-mediated apoptosis and cell proliferation signaling in testis of mice. Free Radic Biol Med 197:15–22. https://doi.org/10.1016/j.freeradbiomed.2023.01.024
Li J, Fu C, Feng B, Liu Q, Gu J, Khan MN et al (2024) Polyacrylic acid-coated selenium-doped carbon dots inhibit ferroptosis to alleviate chemotherapy-associated acute kidney injury. Adv Sci (Weinh) e2400527. https://doi.org/10.1002/advs.202400527
Gustin K, Vahter M, Barman M, Jacobsson B, Skröder H, FilipssonNyström H et al (2022) Assessment of joint impact of iodine, selenium, and zinc status on women’s third-trimester plasma thyroid hormone concentrations. J Nutr 152(7):1737–1746. https://doi.org/10.1093/jn/nxac081
Zhao L, Liu M, Sun H, Yang JC, Huang YX, Huang JQ, Lei X (2023) Sun LH (2023) Selenium deficiency-induced multiple tissue damage with dysregulation of immune and redox homeostasis in broiler chicks under heat stress. Sci China Life Sci 66(9):2056–2069. https://doi.org/10.1007/s11427-022-2226-1
Bielik V, Kolisek M (2021) Bioaccessibility and bioavailability of minerals in relation to a healthy gut microbiome. Int J Mol Sci 22(13):6803. https://doi.org/10.3390/ijms22136803
Yin J, Ren W, Liu G, Duan J, Yang G, Wu L et al (2013) Birth oxidative stress and the development of an antioxidant system in newborn piglets. Free Radic Res 47(12):1027–1035. https://doi.org/10.3109/10715762.2013.848277
Sunde RA (2021) Gene set enrichment analysis of selenium-deficient and high-selenium rat liver transcript expression and comparison with turkey liver expression. J Nutr 151(4):772–784. https://doi.org/10.1093/jn/nxaa333
Zhao L, Sun LH, Huang JQ, Briens M, Qi DS, Xu SW, Lei XG (2017) A novel organic selenium compound exerts unique regulation of selenium speciation, selenogenome, and selenoproteins in broiler chicks. J Nutr 147(5):789–797. https://doi.org/10.3945/jn.116.247338
Zhao L, Chu XH, Liu S, Li R, Zhu YF, Li FN et al (2022) Selenium-enriched Cardamine violifolia increases selenium and decreases cholesterol concentrations in liver and pectoral muscle of broilers. J Nutr 152(9):2072–2079. https://doi.org/10.1093/jn/nxac141
Mou DL, Ding DJ, Li S, Yan H, Qin BT, Li Z et al (2020) Effect of maternal organic selenium supplementation during pregnancy on sow reproductive performance and long-term effect on their progeny. J Anim Sci 98:12. https://doi.org/10.1093/jas/skaa366
Yin LM, Zhang YT, Li J, Zhou J, Wang QY, Huang J et al (2023) Mechanism of iron on the intestinal epithelium development in suckling piglets. Sci China Life Sci 66(9):2070–2085. https://doi.org/10.1007/s11427-022-2307-7
Mor G, Aldo P, Alvero AB (2017) The unique immunological and microbial aspects of pregnancy. Nat Rev Immunol 17(8):469–482. https://doi.org/10.1038/nri.2017.64
** SS, He LQ, Yang CB, He XM, Chen HS, Feng YZ et al (2023) Crosstalk between trace elements and T-cell immunity during early-life health in pigs. Sci China Life Sci 66(9):1994–2005. https://doi.org/10.1007/s11427-022-2339-0
Saraiva M, Vieira P (2020) O’Garra A (2020) Biology and therapeutic potential of interleukin-10. J Exp Med 217:1. https://doi.org/10.1084/jem.20190418
Kapoor M, Martel-Pelletier J, Lajeunesse D, Pelletier JP (2011) Fahmi H (2011) Role of proinflammatory cytokines in the pathophysiology of osteoarthritis. Nat Rev Rheumatol 7(1):33–42. https://doi.org/10.1038/nrrheum.2010.196
Liu C, Chu DW, Kalantar-Zadeh K, George J, Young HA, Liu GZ (2021) Cytokines: from clinical significance to quantification. Adv Sci 8:15. https://doi.org/10.1002/advs.202004433
Cai S, Zhu JL, Zeng XZ, Ye QH, Ye CC, Mao XB, Zhang SH, Qiao SY, Zeng XF (2018) Maternal-carbamylglutamate supply during early pregnancy enhanced pregnancy outcomes in sows through modulations of targeted genes and metabolism pathways. J Agric Food Chem 66(23):5845–5852. https://doi.org/10.1021/acs.jafc.8b01637
Huus KE, Bauer KC, Brown EM, Bozorgmehr T, Woodward SE, Serapio-Palacios A, Boutin RCT, Petersen C, Finlay BB (2020) Commensal bacteria modulate immunoglobulin a binding in response to host nutrition. Cell Host Microbe 27(6):909-921.e905. https://doi.org/10.1016/j.chom.2020.03.012
Li X, **ong X, Wu X, Liu G, Zhou K, Yin YL (2020) Effects of stocking density on growth performance, blood parameters and immunity of growing pigs. Anim Nutr 6(4):529–534. https://doi.org/10.1016/j.aninu.2020.04.001
Zhao K, Yin H, Yan H, Tang W, Diao H, Wang Q, Qi R, Liu J (2023) Dietary supplementation of Lactobacillus johnsonii RS-7 improved antioxidant and immune function of weaned piglets. Animals 13:10. https://doi.org/10.3390/ani13101595
Zhao K, Yin H, Yan H, Tang W, Diao H, Wang Q, Qi R, Liu J (2024) From probiotics to postbiotics: concepts and applications. Anim Res One Health 1(1):92–114. https://doi.org/10.1002/aro2.7
Cao KX, Deng ZC, Liu M, Huang YX, Yang JC, Sun LH (2023) Heat stress impairs male reproductive system with potential disruption of retinol metabolism and microbial balance in the testis of mice. J Nutr 153(12):3373–3381. https://doi.org/10.1016/j.tjnut.2023.10.017
Francis EC, Dabelea D, Boyle KE, Jansson T, Perng W (2022) Maternal diet quality is associated with placental proteins in the placental insulin/growth factor, environmental stress, inflammation, and mtor signaling pathways: the Healthy Start ECHO Cohort. J Nutr 152(3):816–825. https://doi.org/10.1093/jn/nxab403
Sun H, Zhao L, Xu ZJ, De Marco M, Briens M, Yan XH, Sun LH (2021) Hydroxy-selenomethionine improves the selenium status and helps to maintain broiler performances under a high stocking density and heat stress conditions through a better redox and immune response. Antioxidants 10(10):1542. https://doi.org/10.1186/s40104-021-00603-0
Funding
This research was supported in part by the Key R&D Program of Shandong Province, China (2023TZXD038), the Fundamental Research Funds for the Central Universities (Project 2662023DKPY002), and a research gift from Trouw Nutrition.
Author information
Authors and Affiliations
Contributions
Shao-Qing Wang, Hua Sun, and Zhe Peng: animal trials, investigation, methodology, and data analysis; Yan-Ming Han, Bo Zhang, Lane Pineda, Gavin Boerboom, and Ying Liu: writing—review and editing, funding acquisition; Lv-Hui Sun, Zhang-Chao Deng, and Ying Liu: supervision, writing—original draft, visualization, writing—review and editing, and project administration. All authors have read and agreed to the published version of the final manuscript.
Corresponding authors
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.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Wang, SQ., Peng, Z., Sun, H. et al. Evaluating the Impact of an Organic Trace Mineral mix on the Redox Homeostasis, Immunity, and Performance of Sows and their Offspring. Biol Trace Elem Res (2024). https://doi.org/10.1007/s12011-024-04300-7
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s12011-024-04300-7