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Somatic Cell Count Distributions During Lactation Predict Clinical Mastitis

机译:哺乳期的体细胞计数分布可预测临床乳腺炎

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This research investigated somatic cell count (SCC) records during lactation, with the purpose of identifying distribution characteristics (mean and measures of variation) that were most closely associated with clinical mastitis. Three separate data sets were used, one containing quarter SCC (n = 1444) and two containing cow SCC (n = 933 and 11,825). Clinical mastitis was defined as a binary outcome, present or absent, for each lactation, and SCC were log (base 10) transformed. A generalized linear mixed model within a Bayesian framework was used for analysis. Parameters were estimated using Markov Chain Monte Carlo with Gibbs sampling. Results from the 3 data sets were similar. Increased maximum and standard deviation log SCC during lactation, rather than increased geometric mean, were the best overall indicators of clinical mastitis. Distributions of SCC were also investigated separately for different mastitis pathogens. Increased maximum log SCC was associated with clinical mastitis caused by all pathogen types. Increased standard deviation log SCC was associated with Staphylococcus aureus, and Streptococcus uberis clinical mastitis and increased coefficient of variation log SCC (standard deviation divided by mean) was associated with Esche-richia coli clinical mastitis. Increased geometric mean lactation SCC was associated with an increased risk of Staph. aureus clinical mastitis but a reduced risk of E. coli clinical mastitis. Our results suggest that using measures of variation and maximum cow SCC would enhance the accuracy of predicting clinical mastitis, compared with geometric mean SCC, and therefore improve genetic programs that aim to select for clinical mastitis resistance. The results are also consistent with low SCC increasing susceptibility to some mastitis pathogens.
机译:这项研究调查了泌乳过程中的体细胞计数(SCC)记录,目的是确定与临床乳腺炎最密切相关的分布特征(均值和变化量度)。使用了三个单独的数据集,一个包含四分之一的SCC(n = 1444),两个包含了牛SCC(n = 933和11,825)。临床乳腺炎的定义是每次泌乳都存在或不存在二元结局,并且将SCC转化为log(以10为底)。贝叶斯框架内的广义线性混合模型用于分析。使用Markov Chain Monte Carlo和Gibbs采样估计参数。 3个数据集的结果相似。泌乳期间最大和标准偏差log SCC增加,而不是几何平均值增加,是临床乳腺炎的最佳总体指标。还针对不同的乳腺炎病原体分别调查了SCC的分布。最大log SCC增加与所有病原体类型引起的临床乳腺炎有关。标准偏差log SCC增加与金黄色葡萄球菌相关,而乳房链球菌临床乳腺炎和变异系数log SCC增加(标准差除以平均值)与大肠杆菌临床乳腺炎相关。几何平均泌乳SCC的增加与葡萄球菌的风险增加有关。金黄色葡萄球菌临床乳腺炎,但降低大肠杆菌临床乳腺炎的风险。我们的研究结果表明,与几何平均SCC相比,使用变异和最大牛SCC量度将提高预测临床乳腺炎的准确性,并因此改善旨在选择临床乳腺炎抗性的遗传程序。该结果还与低SCC对某些乳腺炎病原体的敏感性增加有关。

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