Barker Samantha N, Jackson Treylr C, Burdick Sanchez Nicole C, Carroll Jeffery A, Broadway Paul R, Hales Kristin E, Ducharme Gary, Legako Jerrad F, Richeson John T
Department of Animal and Food Sciences, Texas Tech University, Lubbock, TX 79413, USA.
Department of Agricultural Sciences, West Texas A&M University, Canyon, TX 79016, USA.
Transl Anim Sci. 2024 Oct 10;8:txae147. doi: 10.1093/tas/txae147. eCollection 2024.
The objective of this study was to evaluate the effects of methionine supplementation prior to and during a lipopolysaccharide (LPS) challenge on the performance and inflammatory biomarkers of receiving beef steers. Steers ( = 65; 295.8 ± 46.5 kg) were randomly assigned to 3 treatment groups: L0 = Control, receiving no supplement; L1 = 10 g/hd/d rumen-protected methionine (MetaSmart, Adisseo USA Inc., Alpharetta, GA); and L2 = 20 g/hd/d rumen-protected methionine and fed for 40 d at the West Texas A&M University Research Feedlot. On day 40, a subset of steers ( = 32; L0 = 10; L1 = 11; L2 = 11) were transported to the USDA Livestock Issues Research Unit, and on day 41 steers were weighed and fitted with indwelling rectal thermometers and jugular catheters. On day 42, steers were challenged i.v. with LPS (0.25 µg/kg BW). Blood samples were collected at -2, 0, 2, 4, 6, 8, 10, 12, 18, 24, 36, and 48 h relative to the LPS administration at 0 h. Serum was isolated to determine serum chemistry and inflammatory marker concentrations. Whole blood was used for hematology analysis. There were no differences in DMI or ADG ( ≥ 0.75) during 35 d of supplementation. A treatment × time interaction ( = 0.01) occurred for rectal temperature, where L2 steers had the greatest temperature following the challenge ( ≤ 0.05) compared to L1 and L0 steers. There was a treatment × time interaction ( = 0.03) for the change in white blood cells where L0 steers had the greatest change compared to L1 and L2 steers at various timepoints. There was a treatment × time interaction ( = 0.02) for the change in tumor necrosis factor-α concentration, where there was a greater increase in concentration in L0 compared to L1 and L2 steers. Additionally, there was a treatment × time interaction ( < 0.01) for Macrophage Inflammatory Protein-1β (MIP-1β) concentrations, where concentrations were greater in L0 compared with L1 and L2 steers from 2 to 4 h post-challenge. There was a treatment × time interaction for plasma total protein concentration ( < 0.01) where L0 steers had less plasma total protein compared with L1 and L2 steers, while L1 steers had less plasma total protein than L2 steers at -2 h prior to LPS challenge. These data suggest that methionine supplementation may have an immunomodulatory effect in beef steers that may improve response to pathogens.
本研究的目的是评估在脂多糖(LPS)刺激之前及期间补充蛋氨酸对育肥肉牛生产性能和炎症生物标志物的影响。将肉牛(n = 65;体重295.8±46.5千克)随机分为3个处理组:L0 = 对照组,不补充任何物质;L1 = 每头每天10克瘤胃保护蛋氨酸(MetaSmart,安迪苏美国公司,美国佐治亚州阿尔法利塔);L2 = 每头每天20克瘤胃保护蛋氨酸,并在西德克萨斯农工大学研究饲养场饲养40天。在第40天,将一部分肉牛(n = 32;L0 = 10头;L1 = 11头;L2 = 11头)转运至美国农业部家畜问题研究单位,在第41天对肉牛称重,并植入直肠温度计和颈静脉导管。在第42天,对肉牛静脉注射LPS(0.25微克/千克体重)。在相对于0小时LPS给药的-2、0、2、4、6、8、10、12、18、24、36和48小时采集血样。分离血清以测定血清生化指标和炎症标志物浓度。全血用于血液学分析。在35天的补充期内,干物质采食量(DMI)或平均日增重(ADG)(P≥0.75)无差异。直肠温度存在处理×时间交互作用(P = 0.01),与L1和L0组肉牛相比,L2组肉牛在刺激后体温最高(P≤0.05)。白细胞变化存在处理×时间交互作用(P = 0.03),在各个时间点,与L1和L2组肉牛相比,L0组肉牛白细胞变化最大。肿瘤坏死因子-α浓度变化存在处理×时间交互作用(P = 0.02),与L1和L2组肉牛相比,L0组肉牛浓度升高幅度更大。此外,巨噬细胞炎性蛋白-1β(MIP-1β)浓度存在处理×时间交互作用(P<0.01),在刺激后2至4小时,与L1和L2组肉牛相比,L0组肉牛MIP-1β浓度更高。血浆总蛋白浓度存在处理×时间交互作用(P<0.01),与L1和L2组肉牛相比,L0组肉牛血浆总蛋白含量较低,而在LPS刺激前-2小时,L1组肉牛血浆总蛋白含量低于L2组肉牛。这些数据表明,补充蛋氨酸可能对育肥肉牛具有免疫调节作用,从而可能改善对病原体的反应。