Test characteristics of milk amyloid A ELISA, somatic cell count, and bacteriological culture for detection of intramammary pathogens that cause subclinical mastitis

被引:22
|
作者
Jaeger, S. [1 ,2 ]
Virchow, F. [2 ]
Torgerson, P. R. [1 ]
Bischoff, M. [2 ]
Biner, B. [2 ]
Hartnack, S. [1 ]
Ruegg, S. R. [1 ]
机构
[1] Univ Zurich, Vetsuisse Fac, Sect Epidemiol, Winterthurerstr 270, CH-8057 Zurich, Switzerland
[2] Clin Alpina SA, Ctr Vet Med, CH-7550 Buorna, Scuol, Switzerland
关键词
subclinical mastitis; somatic cell count; milk amyloid A; bacteriological culture; Bayesian latent class; ACUTE-PHASE PROTEINS; STAPHYLOCOCCUS-AUREUS; DAIRY-COWS; SERUM; PREVALENCE; HAPTOGLOBIN; INFECTIONS; DISEASE; QUARTER; INDICATORS;
D O I
10.3168/jds.2016-12446
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Bovine mastitis is an important disease in the dairy industry, causing economic losses as a result of withheld milk and treatment costs. Several studies have suggested milk amyloid A (MAA) as a promising biomarker in the diagnosis of mastitis. In the absence of a gold standard for diagnosis of subclinical mastitis, we estimated the diagnostic test accuracy of a commercial MAA-ELISA, somatic cell count (SCC), and bacteriological culture using Bayesian latent class modeling. We divided intramammary infections into 2 classes: those caused by major pathogens (e.g., Escherichia coli, Staphylococcus aureus, streptococci, and lacto-/enterococci) and those caused by all pathogens (major pathogens plus Corynebacterium bovis, coagulase-negative staphylococci, Bacillus spp., Streptomyces spp.). We applied the 3 diagnostic tests to all samples. Of 433 composite milk samples included in this study, 275 (63.5%) contained at least 1 colony of any bacterial species; of those, 56 contained major pathogens and 219 contained minor pathogens. The remaining 158 samples (36.5%) were sterile. We determined 2 different thresholds for the MAA-ELISA using Bayesian latent class modeling: 3.9 mu g/mL to detect mastitis caused by major pathogens and 1.6 mu g/mL to detect mastitis caused by all pathogens. The optimal SCC threshold for identification of subclinical mastitis was 150,000 cells/mL; this threshold led to higher specificity (Sp) than 100,000 cells/mL. Test accuracy for major-pathogen intramammary infections was as follows: SCC, sensitivity (Se) 92.6% and Sp 72.9%; MAA-ELISA, Se 81.4% and Sp 93.4%; bacteriological culture, Se 23.8% and Sp 95.2%. Test accuracy for all-pathogen intramammary infections was as follows: SCC, sensitivity 90.3% and Sp 71.8%; MAA-ELISA, Se 88.0% and Sp 65.2%; bacteriological culture, Se 83.8% and Sp 54.8%. We suggest the use of SCC and MAA-ELISA as a combined screening procedure for situations such as a Staphylococcus aureus control program. With Bayesian latent class analysis, we were able to identify a more differentiated use of the 3 diagnostic tools. The MAA-ELISA is a valuable addition to existing tools for the diagnosis of subclinical mastitis.
引用
收藏
页码:7419 / 7426
页数:8
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