Hanigan M D, Souza V C, Martineau R, Daley V L, Kononoff P
Department of Dairy Science, Virginia Tech, Blacksburg 24060.
Department of Dairy Science, Virginia Tech, Blacksburg 24060.
J Dairy Sci. 2021 Aug;104(8):8685-8707. doi: 10.3168/jds.2020-19672. Epub 2021 May 10.
The objectives of the present work were (1) to identify the cause of the linear bias in predictions of rumen-undegradable protein (RUP) content of feeds, and devise methods to remove the bias from prediction equations, and (2) to further explore the impact of rumen-degradable protein (RDP) on microbial N (MiN) outflow from the rumen. The kinetic model used by NRC (2001), which is based on protein fractionation and rates of degradation (Kd) and passage (Kp), displays considerable slope bias (-0.30 kg/kg), indicating parameter or structural problems. Regressing Kp by feed class and a static adjustment factor for the in situ-derived Kd on observed RUP flows completely resolved the slope bias problem, and the model performed significantly better than models using unadjusted Kd and marker-based Kp. The Kd adjustment was 3.82%/h, which represents approximately a 50% increase in rates of degradation over the in situ values, indicating that in situ analyses severely underestimate true rates of protein degradation. The Kp for concentrate-derived protein was 5.83%/h, which was slightly less than the marker-predicted rate of 6.69%/h. However, the derived forage protein rate was 0.49%/h, which was considerably less than the marker-based rate of 5.07%/h. Compartmental analysis of data from a single study corroborated the regression analysis, indicating that a 25% reduction in the overall passage rate and an 87% increase in the rate of degradation were required to align ruminal N pool sizes and the extent of protein degradation with the observed data. Therefore, one must conclude that both the in situ-derived degradation rates and the marker-based particle passage rates are biased relative to protein passage and cannot be used directly to predict RUP outflow from the rumen. The effects of RDP supply on microbial nitrogen (MiN) flow were apparent when intakes of individual nutrients were offered but not when DM intake and individual nutrient concentrations were offered, due to collinearity problems. Microbial N flow from the rumen was found to be linearly related to ruminally degraded starch, ruminally degraded neutral detergent fiber (NDF), RDP, and forage NDF intakes; and quadratically related to residual OM intake. More complicated models containing 2- and 3-way interactions among nutrients were also supported by the data. Independent MiN responses to RDP, ruminally degraded starch, and ruminally degraded NDF aligned with the expected responses to each of those nutrients. Nonlinear representations of MiN were found to be inferior to the linear models. Despite using unbiased predictions of RUP and MiN as drivers of AA flows, predictions of Arg, His, Ile, and Lys flow exhibited linear slope bias relative to the observed data, indicating that representations of the AA composition of the proteins may be biased or the observed data are biased. This is an improvement over the NRC (2001) predictions, where bias adjustments were required for all of the essential AA. Despite the bias for 4 AA flows, the revised prediction system was a substantial improvement over the prior work.
(1)确定饲料瘤胃不可降解蛋白(RUP)含量预测中线性偏差的原因,并设计方法消除预测方程中的偏差;(2)进一步探究瘤胃可降解蛋白(RDP)对瘤胃微生物氮(MiN)流出的影响。美国国家研究委员会(NRC,2001)使用的动力学模型基于蛋白质分级以及降解率(Kd)和通过率(Kp),显示出相当大的斜率偏差(-0.30 kg/kg),表明存在参数或结构问题。通过按饲料类别对Kp进行回归,并对原位测定的Kd使用静态调整因子来拟合观察到的RUP流量,完全解决了斜率偏差问题,且该模型的表现明显优于使用未调整Kd和基于标记物的Kp的模型。Kd调整为3.82%/小时,这意味着降解率比原位测定值大约增加了50%,表明原位分析严重低估了蛋白质的真实降解率。精料来源蛋白质的Kp为5.83%/小时,略低于标记物预测的6.69%/小时。然而,饲草蛋白质的推导率为0.49%/小时,远低于基于标记物的5.07%/小时。对一项单一研究的数据进行的区室分析证实了回归分析结果,表明需要将总体通过率降低25%,降解率提高87%,才能使瘤胃氮库大小和蛋白质降解程度与观察数据相符。因此,必须得出结论,原位测定的降解率和基于标记物的颗粒通过率相对于蛋白质通过率都存在偏差,不能直接用于预测RUP从瘤胃的流出量。当提供单一营养素摄入量时,RDP供应对微生物氮(MiN)流量的影响明显,但当提供干物质摄入量和单一营养素浓度时,由于共线性问题,这种影响不明显。发现瘤胃微生物氮流量与瘤胃降解淀粉、瘤胃降解中性洗涤纤维(NDF)、RDP和饲草NDF摄入量呈线性相关;与残余有机物质摄入量呈二次相关。数据也支持包含营养素之间二元和三元相互作用的更复杂模型。MiN对RDP、瘤胃降解淀粉和瘤胃降解NDF的独立反应与对这些营养素各自的预期反应一致。发现MiN的非线性表示不如线性模型。尽管使用无偏差的RUP和MiN预测作为氨基酸流量的驱动因素,但相对于观察数据,精氨酸、组氨酸、异亮氨酸和赖氨酸流量的预测仍表现出线性斜率偏差,这表明蛋白质氨基酸组成的表示可能存在偏差,或者观察数据存在偏差。这相对于NRC(2001)的预测有所改进,后者对所有必需氨基酸都需要进行偏差调整。尽管4种氨基酸流量存在偏差,但修订后的预测系统比之前的工作有了实质性改进。