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J. Dairy Sci. 87:1256-1264
© American Dairy Science Association, 2004.

Somatic Cell Count Distributions During Lactation Predict Clinical Mastitis

M. J. Green1, L. E. Green1, Y. H. Schukken2, A. J. Bradley3, E. J. Peeler4, H. W. Barkema5, Y. de Haas6, V. J. Collis1 and G. F. Medley1

1 Ecology and Epidemiology Group, Department of Biological Sciences, University of Warwick, Coventry, CV4 7AL, UK
2 Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853
3 Department of Clinical Veterinary Science, University of Bristol, Langford House, Langford, Bristol, BS40 5DT, UK
4 Centre for Environment, Fisheries, Aquaculture Science, Barrack Road, The Nothe, Weymouth, DT4 8UB, UK
5 Dept. of Health Management, Atlantic Veterinary College, University of Prince Edward Island, 550 University Avenue, Charlottetown, PEI, 4P3 C1A Canada
6 Institute for Animal Science and Health (ID-Lelystad), NL-8200 AB Lelystad, The Netherlands

Corresponding author: M. J. Green; e-mail: martingreen1000{at}ntlworld.com.

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 Escherichia 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.

Key Words: mastitis • somatic cell count

Abbreviation key: CM = clinical mastitis, CSCC = cow SCC, QSCC = quarter SCC




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