Title page for ETD etd-08012012-040326

Type of Document Master's Thesis
Author Larson, Ann Michelle
URN etd-08012012-040326
Title Selection for milk somatic cell count in laboratory mice
Degree Master of Science
Department Dairy Science
Advisory Committee
Advisor Name Title
Vinson, William E. Committee Chair
Akers, Robert Michael Committee Member
McGilliard, Michael L. Committee Member
Pearson, Ronald E. Committee Member
  • Mice
Date of Defense 1988-12-15
Availability restricted

A bidirectional selection experiment for high and low somatic cell count (SCC) was conducted over 14 generations with two selected lines (high line = HSCC, low line = LSCC) of mice. Seven secondary traits (milk yield, total white blood cell count, percentage of phagocytic cells in blood, endotoxin challenge response, percentage of females littering, number of young born alive, and percentage of young surviving to weaning) were measured to examine correlated responses to selection for SCC.

Average response per generation for log2 SCC was small in both selected lines (HSCC = .0678 ±.0341, LSCC = .0384 ± .0390, P > .05). There was little per generation divergence between the selected lines (.0294 ± .0178, P > .05). Genetic and phenotypic selection differentials indicated that selection procedures did select the more extreme individuals for SCC, even though response to selection was poor.

Phenotypic correlations among SCC and the seven secondary traits were generally small, and near zero. Correlation coefficients ranged from -.17 to .17. Milk yield was negatively correlated with SCC (-.07, P < .05). The correlation between endotoxin challenge response and SCC was also negative (-.17, P < .05).

Components of genetic variance for SCC were estimated to explain the lack of selection response. Covariances between daughter and dam, and among full sibs were negative (-.1180 and -.0362, respectively). Analysis for offspring and maternal components for SCC yielded a negative estimate for the covariance between additive effects for the offspring and maternal components (-.1781). No biological explanation can be offered for its existence. Heritability from this same analysis was .05.

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