Instituto de Ganadería de Montaña (CSIC-Universidad de León), Finca Marzanas s/n, 24346 Grulleros, León, Spain.
J Dairy Sci. 2012 Feb;95(2):794-806. doi: 10.3168/jds.2011-4561.
Supplementation of ruminant diets with plant oils and marine lipids is an effective strategy for lowering saturated fatty acid (FA) content and increasing the concentration of cis-9,trans-11 conjugated linoleic acid and long-chain n-3 FA in ruminant milk. However, changes in populations of ruminal microorganisms associated with altered biohydrogenation of dietary unsaturated FA are not well characterized. Twenty-five lactating Assaf ewes were allocated at random to 1 of 5 treatments composed of dehydrated alfalfa hay and concentrates containing no additional lipid (control), or supplemented with 25 g of sunflower oil and 0 (SO), 8 (SOMA(1)), 16 (SOMA(2)), or 24 (SOMA(3)) g of marine algae/kg of diet dry matter. On d 28 on diet, samples of rumen fluid were collected for lipid analysis and microbial DNA extraction. Appearance and identification of biohydrogenation intermediates was determined based on complementary gas chromatography and Ag+-HPLC analysis of FA methyl esters. Total bacteria and the Butyrivibrio group were studied in microbial DNA by terminal RFLP analysis, and real-time PCR was used to quantify the known Butyrivibrio bacteria that produce trans-11 18:1 or 18:0. Dietary supplements of sunflower oil alone or in combination with marine algae altered the FA profile of rumen fluid, which was associated with changes in populations of specific bacteria. Inclusion of marine algae in diets containing sunflower oil resulted in the accumulation of trans 18:1 and 10-O-18:0 and a marked decrease in 18:0 concentrations in rumen fluid. At the highest levels of supplementation (SOMA(2) and SOMA(3)), marine algae also promoted a shift in ruminal biohydrogenation pathways toward the formation of trans-10 18:1 at the expense of trans-11 18:1. Changes in the concentration of biohydrogenation intermediates were not accompanied by significant variations in the abundance of known cultivated ruminal bacteria capable of hydrogenating unsaturated FA. However, certain bacterial groups detected by terminal RFLP (such as potentially uncultured Lachnospiraceae strains or Quinella-related bacteria) exhibited variations in their relative frequency consistent with a potential role in one or more metabolic pathways of biohydrogenation in the rumen.
反刍动物日粮中添加植物油和海洋脂质是降低饱和脂肪酸(FA)含量并增加反式-9,顺式-11 共轭亚油酸和长链 n-3 FA 在反刍动物奶中浓度的有效策略。然而,与膳食不饱和 FA 生物氢化改变相关的瘤胃微生物种群的变化尚不清楚。25 只泌乳期 Assaf 母羊随机分配到 5 种处理中的 1 种,处理组日粮由脱水紫花苜蓿干草和不含额外脂质的浓缩饲料组成(对照组),或添加 25 g 葵花籽油和 0(SO)、8(SOMA(1))、16(SOMA(2))或 24(SOMA(3))g 海洋藻类/kg 日粮干物质。在第 28 天的日粮期,收集瘤胃液样品进行脂质分析和微生物 DNA 提取。根据 FA 甲酯的互补气相色谱和 Ag+-HPLC 分析,确定生物氢化中间产物的外观和鉴定。通过末端 RFLP 分析研究微生物 DNA 中的总细菌和丁酸弧菌属,实时 PCR 用于定量产生反式-11 18:1 或 18:0 的已知丁酸弧菌。单独添加葵花籽油或与海洋藻类联合添加改变了瘤胃液的 FA 谱,这与特定细菌种群的变化有关。在含有葵花籽油的日粮中添加海洋藻类会导致反式 18:1 和 10-O-18:0 的积累以及瘤胃液中 18:0 浓度的显著下降。在最高添加水平(SOMA(2)和 SOMA(3))下,海洋藻类还促进了瘤胃生物氢化途径向反式-10 18:1 的形成转变,而反式-11 18:1 的形成减少。生物氢化中间产物浓度的变化没有伴随着能够氢化不饱和 FA 的已知培养瘤胃细菌丰度的显著变化。然而,通过末端 RFLP 检测到的某些细菌群(例如潜在未培养的 Lachnospiraceae 菌株或与 Quinella 相关的细菌)的相对频率发生了变化,这与它们在瘤胃生物氢化的一个或多个代谢途径中的潜在作用一致。