Department of Animal Science, University of Padova, Legnaro (PD), Italy.
J Dairy Sci. 2011 Sep;94(9):4336-46. doi: 10.3168/jds.2011-4267.
Milk coagulation properties (MCP) analysis is performed using a wide range of methodologies in different countries and laboratories, using different instruments, coagulant activity in the milk, and type of coagulant. This makes it difficult to compare results and data from different research. The aims of this study were to propose a method for the transformation of values of rennet coagulation time (RCT) and curd firmness (a(30)) and to predict the noncoagulation (NC) probability of milk samples analyzed using different methodologies. Individual milk samples were collected during the morning milking in October 2010 from each of 165 Holstein-Friesian dairy cows in 2 freestall barns in Italy, and sent to 3 laboratories for MCP analysis. For each laboratory, MCP analysis was performed using a different methodology: A, with a computerized renneting meter instrument using 0.051 international milk clotting units (IMCU)/mL of coagulant activity; B, with a Lattodinamografo (Foss-Italia, Padova, Italy) using 0.051 IMCU/mL of coagulant activity; and C, with an Optigraph (Ysebaert, Frépillon, France) using 0.120 IMCU/mL of coagulant activity. The relationships between MCP traits were analyzed with correlation and regression analyses for each pair of methodologies. For each MCP trait, 2 regression models were applied: model 1 was a single regression model, where the dependent and independent variables were the same MCP trait determined by 2 different methodologies; in model 2, both a(30) and RCT were included as independent variables. The NC probabilities for laboratories with the highest number of NC samples were predicted based on the RCT and a(30) values measured in the laboratories with lower number of NC samples using logistic regression and receiver operating characteristic analysis. The percentages of NC samples were 4.2, 11.5, and 0.6% for A, B, and C, respectively. The transformation of MCP traits was more precise with model 1 for RCT (R(2): 0.77-0.82) than for a(30) (R(2): 0.28-0.63). The application of model 2 was needed when the C measurements were transformed into the other scales. The analyses of NC probabilities of milk samples showed that NC samples from one methodology were well distinguishable (with an accuracy of 0.972-0.996) based on the rennet coagulation time measured with the other methodology. A standard definition for MCP traits analysis is needed to enable reliable comparisons between MCP traits recorded in different laboratories and in different animal populations and breeds.
牛奶凝固特性(MCP)分析在不同国家和实验室中使用多种方法进行,使用不同的仪器、牛奶中的凝固酶活性和凝固剂类型。这使得比较来自不同研究的数据变得困难。本研究的目的是提出一种转化凝乳酶凝固时间(RCT)和凝块强度(a(30))值的方法,并预测使用不同方法分析的牛奶样品的非凝固(NC)概率。2010 年 10 月,在意大利的 2 个自由放养牛舍中,从每头荷斯坦-弗里森奶牛中采集了清晨挤奶的个体牛奶样本,并发送到 3 个实验室进行 MCP 分析。对于每个实验室,使用不同的方法进行 MCP 分析:A 法,使用计算机凝乳酶计,使用 0.051 国际牛奶凝固单位(IMCU)/mL 的凝固酶活性;B 法,使用 Lattodinamografo(Foss-Italia,帕多瓦,意大利),使用 0.051 IMCU/mL 的凝固酶活性;和 C 法,使用 Optigraph(Ysebaert,弗雷皮永,法国),使用 0.120 IMCU/mL 的凝固酶活性。对于每对方法,使用相关和回归分析分析 MCP 特征之间的关系。对于每个 MCP 特征,应用了 2 个回归模型:模型 1 是一个单一的回归模型,其中依赖变量和独立变量是由 2 种不同方法确定的相同 MCP 特征;在模型 2 中,将 a(30)和 RCT 都包含为独立变量。根据在 NC 样品数量较少的实验室中测量的 RCT 和 a(30)值,使用逻辑回归和接收者操作特征分析对具有最高数量 NC 样品的实验室的 NC 样品概率进行预测。A、B 和 C 实验室的 NC 样品百分比分别为 4.2%、11.5%和 0.6%。RCT(R(2):0.77-0.82)的模型 1 比 a(30)(R(2):0.28-0.63)更精确地转换 MCP 特征。当将 C 测量值转换为其他比例时,需要应用模型 2。NC 样品概率分析表明,基于用其他方法测量的凝乳酶凝固时间,可以很好地区分(准确性为 0.972-0.996)来自一种方法的 NC 样品。需要对 MCP 特征分析进行标准化定义,以便能够在不同实验室和不同动物群体和品种中记录的 MCP 特征之间进行可靠的比较。