Department of Animal and Poultry Science, University of Saskatchewan, Saskatoon, SK S7N 5A8, Canada.
Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK S7N 5A8, Canada.
J Dairy Sci. 2019 Aug;102(8):7556-7569. doi: 10.3168/jds.2019-16294. Epub 2019 Jun 20.
The aim of this study was to investigate whether the ruminal epithelium activates a local inflammatory response following a short-term subacute ruminal acidosis (SARA) challenge. Seven ruminally cannulated, nonpregnant, nonlactating beef heifers, fed a baseline total mixed ration (TMR) with 50:50 forage-to-concentrate ratio, were used in a crossover design with 2 periods and 2 treatments: SARA and control (CON). Induction of SARA included feed restriction (25% of dry matter intake [DMI] for 24 h) followed by a grain overload (30% of baseline DMI) and provision of the full TMR; whereas, the CON group received the TMR ad libitum. Ruminal pH was recorded using indwelling probes, and ruminal lipopolysaccharide (LPS) concentration was measured daily following the challenge until d 6. Biopsies of ruminal papillae from the ventral sac were collected on d 2 and 6 after the grain overload. Transcript abundance of genes associated with acute inflammation was measured by quantitative real-time PCR, normalized to the geometric mean of 3 stable housekeeping genes. Target genes included toll-like receptor-2 (TLR2), TLR4, TLR9, tumor necrosis factor-α (TNFA), prostaglandin endoperoxide synthase-1 (PTGS1), PTGS2 transforming growth factor β-1 (TGFB1), and 4 intermediate enzymes of leukotriene synthesis (ALOX5, ALOX5AP, LTA4H, and LTC4S). Protein localization and expression of TLR4 were quantified by image analysis of fluorescence intensity. Statistical analysis was performed using as a crossover design with fixed effects of treatment, day, and the treatment × day interaction with the random effect of day within period. Ruminal pH was below 5.6 for 4.5 h/d and below 5.8 for 6.9 h/d in the SARA group compared with 22 and 72 min/d, respectively, for CON. Ruminal LPS concentration peaked on d 2 in SARA heifers at 51,481 endotoxin units (EU)/mL compared with 13,331 EU/mL in CON. Following grain overload, small but statistically significant decreases in the transcriptional abundance of TLR2, TLR4, TNF, PTGS2, ALOX5, and ALOX5AP were seen in SARA versus CON heifers. A functionally relevant decrease in TLR4 expression in SARA heifers compared with CON was confirmed by a decrease in fluorescence intensity of the corresponding protein following immunohistofluorescent staining of papillae. The study results indicate a suppression of the inflammatory response in the ruminal epithelium and suggest that the response is tightly regulated, allowing for tissue recovery and return to homeostasis following SARA.
本研究旨在探讨短期亚急性瘤胃酸中毒(SARA)挑战后,瘤胃上皮是否会引发局部炎症反应。选用 7 头装有瘤胃套管、非妊娠、非泌乳的肉牛,以 50:50 的粗饲料-精饲料比进行基础全混合日粮(TMR)饲养,采用交叉设计,分为 2 个时期和 2 个处理:SARA 和对照(CON)。SARA 的诱导包括饲料限制(24 小时内干物质摄入量的 25%),然后进行谷物过载(基础 DMI 的 30%)和提供完整的 TMR;而 CON 组则自由采食 TMR。使用植入式探针记录瘤胃 pH 值,在谷物过载后每天测量瘤胃内毒素(LPS)浓度,直到第 6 天。在谷物过载后的第 2 天和第 6 天,从腹囊的瘤胃乳头采集活检样本。通过实时定量 PCR 测量与急性炎症相关的基因的转录丰度,并标准化为 3 个稳定管家基因的几何平均值。靶基因包括 Toll 样受体 2(TLR2)、TLR4、TLR9、肿瘤坏死因子-α(TNFA)、前列腺素内过氧化物合酶 1(PTGS1)、PTGS2 转化生长因子-β-1(TGFB1)和白细胞三烯合成的 4 个中间酶(ALOX5、ALOX5AP、LTA4H 和 LTC4S)。通过荧光强度的图像分析定量 TLR4 的蛋白定位和表达。采用交叉设计,固定效应为处理、天和处理×天互作,随机效应为时期内的天,进行统计分析。SARA 组的瘤胃 pH 值低于 5.6 的时间为 4.5 小时/天,低于 5.8 的时间为 6.9 小时/天,而 CON 组分别为 22 分钟/天和 72 分钟/天。在 SARA 奶牛中,瘤胃 LPS 浓度在第 2 天达到峰值,为 51481 内毒素单位(EU)/mL,而 CON 组为 13331 EU/mL。在谷物过载后,SARA 奶牛中 TLR2、TLR4、TNF、PTGS2、ALOX5 和 ALOX5AP 的转录丰度均出现小但具有统计学意义的下降,与 CON 奶牛相比。通过对乳头进行免疫荧光染色,确认 TLR4 蛋白的相应荧光强度下降,证实 SARA 奶牛 TLR4 表达存在功能相关的下降。研究结果表明,瘤胃上皮的炎症反应受到抑制,并表明该反应受到严格调控,允许组织恢复并在 SARA 后恢复到体内平衡。