4.7 Article

Monitoring dry period intramammary infection incidence and elimination rates using somatic cell count measurements

Journal

JOURNAL OF DAIRY SCIENCE
Volume 95, Issue 12, Pages 7173-7185

Publisher

ELSEVIER SCIENCE INC
DOI: 10.3168/jds.2012-5839

Keywords

dry period; intramammary infection; incidence; somatic cell count

Funding

  1. Natural Sciences and Engineering Research Council of Canada (Ottawa, ON, Canada)
  2. Alberta Milk (Edmonton, AB, Canada)
  3. Dairy Farmers of New Brunswick (Sussex, NB, Canada)
  4. Dairy Farmers of Nova Scotia (Lower Truro, NS, Canada)
  5. Dairy Farmers of Ontario (Mississauga, ON, Canada)
  6. Dairy Farmers of Prince Edward Island (Charlottetown, PE, Canada)
  7. Novalait Inc. (Quebec City, QC, Canada)
  8. Dairy Farmers of Canada (Ottawa, ON, Canada)
  9. Canadian Dairy Network (Guelph, ON, Canada)
  10. Agriculture and Agri-Food Canada (Ottawa, ON, Canada)
  11. Public Health Agency of Canada (Ottawa, ON, Canada)
  12. Technology PEI Inc. (Charlottetown, PE, Canada)
  13. Universite de Montreal (Montreal, QC, Canada)
  14. University of Prince Edward Island, through the Canadian Bovine Mastitis Research Network (Saint-Hyacinthe, QC, Canada)

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The objective of the study was to evaluate the predictive ability of the herd dry period (DP) intramammary infection (IMI) incidence and elimination rates derived from predry and postcalving somatic cell count (SCC) measurements [quarter-level SCC and dairy herd improvement (DHI) composite-level SCC] for monitoring the herd DP IMI incidence and elimination rates. A cohort of 91 Canadian dairy herds was followed from 2007 to 2008. In each herd, a sample of 15 cows was selected each year, and a series of 2 predry and 2 postcalving quarter milk samples were collected. Routine milk bacteriological culture was conducted to identify EVIL SCC was measured on the quarter milk samples, and composite SCC of the last predry and first postcalving DHI. tests were obtained. Mastitis pathogens were grouped into 3 categories: major pathogens, minor pathogens, and any pathogens. For each herd, DP bacteriological culture-derived IMI incidence and elimination rates were computed using quarter milk culture data. Similarly, SCC-derived herd incidence and elimination rates were computed using quarter and DHI composite-level SCC measurements and using various SCC thresholds to define new and eliminated IMI. Linear regression was used to compare herd quarter-level and composite-level SCC-derived herd incidence and elimination with DP bacteriological culture-derived IMI incidence and elimination. Herd DP incidences computed by using quarter-level SCC, and with most of the SCC thresholds tested, were significant predictors of the DP major, minor, and any IMI incidences (F-test; P <= 0.05). The highest coefficients of determination (R-2) were obtained with thresholds of 200,000 (R-2: 12%) and 50,000 cells/mL (R-2: 25%) for predicting major and minor Evil, respectively. When using composite DHI SCC measurements, however, substantial losses of predictive power were seen for minor and any IMI incidences compared with quarter-level SCC. For DP major IMI incidence, composite SCC yielded similar, but modest, predictive power when a cutoff value of 150,000 cells/mL was chosen to define new EVIL To predict DP elimination rates, the value of quarter-level SCC seemed limited to predicting the DP major IMI elimination rate. Composite SCC, on the other hand, showed modest predictive power for major and minor TAU elimination rates, with thresholds of 200,000 and 50,000 cells/mL, respectively Results from the current study suggest that quarter and composite SCC-derived rates could be used as substitutes for bacteriological culture-derived rates for some groups of mastitis pathogens.

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