AWET Undergraduate Project Scholarship 2014 Summary Report

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AWET Undergraduate Project Scholarship 2014 Summary Report Supplementation of Merino ewes with cholecalciferol in late pregnancy improves the Vitamin D status of ewes and lambs at birth but is not correlated with an improvement in immune function in lambs Amy Lockwood Supervisors: Dr. Andrew Thompson, Dr. Andrew Currie & Dr. Serina Hancock (Murdoch University) Introduction On average, 30% of all lambs born will die prior to weaning, and approximately 80% of lamb deaths occur in the first 48 to 72 hours of life (Miller et al. 2010; Oldham et al. 2011; Hawken et al. 2012; Hinch and Brien 2014; Paganoni et al. 2014). Lamb birthweight is the greatest contributor to lamb survival however, even when birthweights are optimised, lamb survival to weaning rarely exceeds 90% for singles, 75% for multiples and 60% for triplets (Oldham et al. 2011; Hinch and Brien 2014; Paganoni et al. 2014), suggesting that factors independent of birthweight must also influence lamb survival. Immune competency has been linked to survival in other neonatal mammals (Zhao et al. 2008; Merlot et al. 2013), however its role in the mortality of lambs is poorly understood. Functional deficiencies in the innate and adaptive immune systems, including in phagocytosis and the development of antibody-mediated immunity, are known to predispose neonates to infection and the associated inflammation, which may cause tissue damage and/or dysfunction, and death, particularly in the perinatal period (Firth et al. 2005; Futata et al. 2012). Furthermore, an increased genetic potential for CFW has been reported to compromise lamb survival and may be due to competition between the immune system and wool follicles for essential nutrients (Lee et al. 1993; Liu et al. 2005; Williams 2011; Brien et al. 2014). Therefore, lambs with a higher genetic potential for fleece weight may have more compromised immune systems and be at increased risk of dying. Vitamin D has been recognised to have several roles in the regulation of immune function and can enhance innate antimicrobial immune responses, whilst dampening excessive adaptive immune responses and inflammation (Lang et al. 2013). Maternal requirements for Vitamin D are increased during pregnancy (Lucas et al. 2008) and Vitamin D is transferred across the placenta to the fetus (Kovacs 2008; Lapillonne 2010). Increased Vitamin D levels in ewes and neonatal lambs may therefore be associated with a greater ability to control infection and/or limit infection-driven inflammation, and thus may contribute to improved lamb survival. Supplementation of ewes with Vitamin D during pregnancy may therefore increase the levels of Vitamin D in the ewe and her lamb/s, thereby improving innate and/or adaptive immunity in the ewe, and innate and/or passive immunity in the lamb. 1

This study therefore tested the hypotheses that; (i Maternal supplementation of Merino ewes with cholecalciferol during late pregnancy increases the levels of Vitamin D in the ewe and lamb at birth, (ii) Maternal supplementation of Merino ewes with cholecalciferol during late pregnancy is correlated with increased innate phagocytic and adaptive antibody responses in the lamb, and (iii) The effect of maternal cholecalciferol supplementation on lamb immune function will be greater in lambs with a higher genetic potential for fleece weight. Experimental design Two hundred Merino ewes aged between 4 and 7 years old were sourced from the Maternal Efficiency Flock. The ewes were artificially inseminated with semen from four sires specifically selected to have different ASBVs for clean fleece weight at yearling age (YCFW) in order to assess the differences in immune responses between lambs with higher and lower genetic potential for fleece weight, where L1 and L2 are the sires with a low genetic potential for YCFW and H1 and H2 are the sires with a high genetic potential for YCFW. On day 111 pregnancy the ewes were allocated into three replicates of two treatment groups; Control or Vitamin D supplementation during late pregnancy. The Control group (n = 58) consisted of ewes receiving no additional nutritional treatments. Ewes supplemented with Vitamin D (n = 53) received an injection of cholecalciferol (Vitamin D 3 ) at days 113 and 141 of pregnancy. On each occasion, 1.0 x 10 6 IU cholecalciferol, in oil, was injected intramuscularly into the hind-limb. Blood samples were collected from Vitamin D and Control ewes prior to treatments, on day 111 of pregnancy, for subsequent analysis of Vitamin D concentrations. At lambing ewes were intensively monitored in order for ewe and lamb sampling to occur prior to the lamb suckling following birth. At birth, all lambs were weighed, and their dam, sex and birth type was recorded (n = 154). Blood samples were collected from all single-born lambs and the first lamb born only for those born in litters for subsequent Vitamin D and immunological analysis. Rectal temperatures and blood glucose concentrations of the lambs were measured where possible. Colostrum and blood samples were collected from all ewes for immunological and Vitamin D analysis respectively. Lambs were bled again at 1-, 4-, 6- and 14- weeks of age for subsequent Vitamin D and/or immunological analysis. Lambs were marked and given their primary vaccinations at 4-weeks of age and were weaned at 14- weeks of age. Ewes were weighed and body condition scored every 1-2 weeks prior to lambing and both ewes and lambs were weighed every 2-3 weeks between lambing and weaning. The Vitamin D status of the ewes and lambs was assessed by measuring the total concentration of 25-hydroxyvitamin D in plasma. Lamb immune function was assessed by analysing the functional capacity of phagocytes (monocytes and polymorphonuclear leukocytes), and the plasma immunoglobulin-g and anti-tetanus-toxoid antibody concentrations between birth and weaning. Statistical analyses were performed using GENSTAT (VSN International 2012). The data was assessed using Restricted Maximum Likelihood and Generalized Linear Mixed Models, where 2

appropriate. Data was angular or log-transformed where necessary and is presented in the backtransformed state. Statistical significance was accepted at P < 0.05. Summary of Results Maternal supplementation with cholecalciferol in late pregnancy increased the plasma concentrations of 25(OH)D in supplemented ewes by 74% at lambing and this doubled the plasma 25(OH)D concentrations in their lambs at birth (Table 1). The plasma 25(OH)D concentrations of ewes and lambs were positively correlated at lambing, confirming that 25(OH)D crosses the placenta in ewes to increase the plasma 25(OH)D concentrations of the fetus and neonate. These findings support our first hypothesis. However, lambs born to both Vitamin D-supplemented and Control ewes were likely to be Vitamin D-deficient at both birth and 4-weeks of age. There is no data available on critical plasma 25(OH)D concentrations in adult or neonatal sheep, but in humans plasma 25(OH)D concentrations of < 50 nmol/l are generally classified as Vitamin D-deficient (Lucas et al. 2008; Holick 2009; Principi et al. 2013; Thiele et al. 2013). Table 2. Mean plasma total 25-hydroxyvitamin D concentrations (nmol/l) of Control and Vitamin D-supplemented ewes prior to supplementation (day 111 pregnancy), at lambing and 4- weeks after lambing, and of their lambs at birth and 4-weeks of age. The ewes were supplemented with cholecalciferol on days 113 and 141 of pregnancy. Values are presented in the back-transformed state where appropriate. Control Vitamin D P value Ewes Pre-treatment 66.3 72.5 0.259 Lambing 78.6 137.0 < 0.001 4-weeks 73.0 157.0 < 0.001 Lambs Birth 24.2 49.0 < 0.001 4-weeks 21.9 25.6 0.168 There were no significant differences between lambs from Control and Vitamin D-supplemented ewes in the percentages of phagocytic monocytes or PMNL in whole blood at birth (84.2 vs 85% and 60.0 vs 60.2%, respectively) or 4-weeks of age (98.6 vs 98.2% and 91.2 vs 92.8%, respectively). The concentration of IgG in the colostrum of Control and Vitamin D ewes did not differ significantly (80.4 vs 82.3 mg/ml) and there was no significant effect of maternal supplementation on the concentrations of IgG in the plasma of lambs between birth and weaning (Figure 1). Maternal supplementation had 3

no effect on the vaccine-specific antibody response against tetanus-toxoid in lambs between birth and weaning. Therefore our second hypothesis was rejected. The genetic potential of the lamb for YCFW had no significant effect on the competency of its immune system, therefore our third hypothesis was also rejected. However, the lack of improvement in the immune function of the lamb may be explained by the poor Vitamin D status of the lambs. We did not examine the antimicrobial killing capacities of phagocytes or the inflammatory responses in the lamb and therefore further research could investigate the relationship between the plasma Vitamin D levels in the lambs and these immune measures. 20 Plasma total IgG concentra:on (mg/ml) 18 16 14 12 10 8 6 4 2 0 Passive immunity Primary vaccinations 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Lamb age (weeks) Weaning Fig. 2. Mean plasma total IgG concentrations (± least significant intervals) of Control (blue) and Vitamin D (red) lambs at birth and 1-, 4-, 6- and 14-weeks of age. The ewes were supplemented with cholecalciferol on days 113 and 141 of pregnancy. Values are presented in the back-transformed state. Maternal supplementation with cholecalciferol in late pregnancy did not have any significant effect on the liveweights or body condition scores of the ewes between artificial insemination and weaning, and there was no effect of maternal supplementation or the genetic potential of the lamb for YCFW on the liveweights of lambs between birth and weaning or the rectal temperatures or blood glucose concentrations of lambs at birth. There was no significant difference in the survival of Vitamin D or Control lambs to weaning (80.8 vs 69.9% ; P = 0.186). On average, only 4.6% of lambs born alive died within the first 72 hours of life in the present study, which is considerably lower than the expected mortality of 20 30% (Oldham et al. 2011; Hawken et al. 2012; Hinch and Brien 2014). We therefore expect that the limited number of lamb deaths during this high risk period was due to the 4

high level of intervention associated with intensive sampling at lambing. Nevertheless, lambs sired by L1 (87.9%) tended to have lower survival to weaning than lambs sired by H2 (72.3% ; P = 0.079), which represent the sires with the highest and lowest genetic potential for YCFW, respectively. Whilst the differences are unlikely to be related to differences in immune function, these findings support those of previous studies which have identified negative correlations between lamb survival and the genetic potential for CFW (Adams et al. 2006; Safari et al. 2007; Brien et al. 2014) and suggest further research into the correlation between CFW and lamb survival is warranted. Overall our novel findings showed that supplementation of ewes with two large intramuscular doses of 1 x 10 6 IU cholecalciferol in late pregnancy is inadequate in boosting the immune competency of the lamb and may be due to the immune system not being responsive to Vitamin D- supplementation if the lamb is in a Vitamin D-deficient state. Further research is therefore required to determine the requirements for Vitamin D in adult and neonatal sheep and additionally what levels of Vitamin D are required to optimize immune function. Subsequent research could then determine what approach to Vitamin D-supplementation is most effective at safely boosting the immune competency of the lamb and if this is associated with an improvement in lamb survival. References Adams NR, Briegel JR, Greeff JC, Bermingham EN (2006) Feed intake, body composition, and plasma metabolic hormones in Merino sheep that differ genetically in fleece weight or fibre diameter. Australian Journal of Agricultural Research 57, 27-32. Brien FD, Cloete SWP, Fogarty NM, Greeff JC, Hebart ML, Hiendleder S, Edwards JEH, Kelly JM, Kind KL, Kleemann DO, Plush KL, Miller DR (2014) A review of the genetic and epigenetic factors affecting lamb survival. Animal Production Science 54, 667-693. Firth MA, Shewen PE, Hodgins DC (2005) Passive and active components of neonatal innate immune defenses. Animal Health Research Reviews 6, 143-58. Futata EA, Fusaro AE, de Brito CA, Sato MN (2012) The neonatal immune system: immunomodulation of infections in early life. Expert Review of Anti-infective Therapy 10, 289-298. Hawken PAR, Williman M, Milton J, Kelly R, Nowak R, Blache D (2012) Nutritional supplementation during the last week of gestation increased the volume and reduced the viscosity of colostrum produced by twin bearing ewes selected for nervous temperament. Small Ruminant Research 105, 308-314. Hinch GN, Brien F (2014) Lamb survival in Australian flocks: a review. Animal Production Science 54, 656-666. Holick MF (2009) Vitamin D Status: Measurement, Interpretation, and Clinical Application. Annals of Epidemiology 19, 73-78. 5

Kovacs CS (2008) Vitamin D in pregnancy and lactation: maternal, fetal, and neonatal outcomes from human and animal studies. The American Journal of Clinical Nutrition 88, 520S-528S. Lang PO, Samaras N, Samaras D, Aspinall R (2013) How important is Vitamin D in preventing infections? Osteoporosis International 24, 1537-1553. Lapillonne A (2010) Vitamin D deficiency during pregnancy may impair maternal and fetal outcomes. Medical Hypotheses 74, 71-75. Lee J, Harris PM, Sinclair BR, Treloar BP (1993) Whole body metabolism of cysteine and glutathione and their utilization in the skin of Romney sheep: consequences for wool growth. The Journal of Agricultural Science 121, 111-124. Liu SM, Smith TL, Karlsson LJE, Palmer DG, Besier RB (2005) The costs for protein and energy requirements by nematode infection and resistance in Merino sheep. Livestock Production Science 97, 131-139. Lucas RM, Ponsonby A-L, Pasco JA, Morley R (2008) Future health implications of prenatal and early-life Vitamin D status. Nutrition Reviews 66, 710-720. Merlot E, Quesnel H, Prunier A (2013) Prenatal stress, immunity and neonatal health in farm animal species. Animal 7, 2016-2025. Miller DR, Blache D, Jackson RB, Downie EF, Roche JR (2010) Metabolic maturity at birth and neonate lamb survival: Association among maternal factors, litter size, lamb birth weight, and plasma metabolic and endocrine factors on survival and behavior. Journal of Animal Science 88, 581-593. Oldham CM, Thompson AN, Ferguson MB, Gordon DJ, Kearney GA, Paganoni BL (2011) The birthweight and survival of Merino lambs can be predicted from the profile of liveweight change of their mothers during pregnancy. Animal Production Science 51, 776-783. Paganoni BL, Ferguson MB, Kearney GA, Thompson AN (2014) Increasing weight gain during pregnancy results in similar increases in lamb birthweights and weaning weights in Merino and non-merino ewes regardless of sire type. Animal Production Science 54, 727-735. Principi N, Bianchini S, Baggi E, Esposito S (2013) Implications of maternal Vitamin D deficiency for the fetus, the neonate and the young infant. European Journal of Nutrition 52, 859-867. Safari E, Fogarty NM, Gilmour AR, Atkins KD, Mortimer SI, Swan AA, Brien FD, Greeff JC, Van Der Werf JHJ (2007) Genetic correlations among and between wool, growth and reproduction traits in Merino sheep. Journal of Animal Breeding and Genetics 124, 65-72. Thiele DK, Thiele DK, Senti JL, Anderson CM (2013) Maternal Vitamin D Supplementation to Meet the Needs of the Breastfed Infant: A Systematic Review. Journal of Human Lactation 29, 163-12 VSN International (2012) GENSTAT for Windows. 15th edn. (VSN International: Hemel Hempstead, UK) 6

Williams AR (2011) Immune-mediated pathology of nematode infection in sheep - is immunity beneficial to the animal? Parasitology 138, 547-56. Zhao J, Kim KD, Yang X, Auh S, Fu Y-X, Tang H (2008) Hyper innate responses in neonates lead to increased morbidity and mortality after infection. Proceedings of the National Academy of Sciences 105, 7528-7533. 7