Genetic analysis of clinical mastitis, milk fever, ketosis, and retained placenta in three lactations of Norwegian Red cows

被引:94
作者
Heringstad, B [1 ]
Chang, YM
Gianola, D
Klemetsdal, G
机构
[1] Norwegian Univ Life Sci, Dept Anim & Aquacultural Sci, N-1432 As, Norway
[2] Geno Breeding & Al Associates, N-1432 As, Norway
[3] Univ Wisconsin, Dept Dairy Sci, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
dairy cattle; disease; genetic correlation; threshold model;
D O I
10.3168/jds.S0022-0302(05)73010-1
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The objectives were to infer heritability and genetic correlations between clinical mastitis (CM), milk fever (MF), ketosis (KET), and retained placenta (RP) within and between the first 3 lactations and to estimate genetic change over time for these traits. Records of 372,227 daughters of 2411 Norwegian Red (NRF) sires were analyzed with a 12-variate (4 diseases x 3 lactations) threshold model. Within each lactation, absence or presence of each of the 4 diseases was scored based on the cow's health recordings. Each disease was assumed to be a different trait in each of the 3 lactations. The model for liability had trait-specific effects of year-season of calving and age of calving (first lactation) or month-year of calving and calving interval (second and third lactations), herd-5-yr, sire of the cow, and a residual. Posterior means of heritability of liability in first, second, and third lactations were 0.08, 0.07, and 0.07, respectively, for CM; 0.09, 0.11, and 0.13 for MF; 0.14, 0.16, and 0.15 for KET, and 0.08 in all 3 lactations for RP. Posterior means of genetic correlations between liability to CM, MF, KET, and RP, within disease between lactations, ranged from 0.19 to 0.86, and were highest between KET in different lactations. Correlations involving first lactation MF were low and had higher standard deviations. Genetic correlations between diseases were low or moderate (from -0.10 to 0.40), within as well as between lactations; the largest estimates were for MF and KET, and the lowest involved MF or KET and RP. Positive genetic correlations between diseases suggest that some general disease resistance factor with a genetic component exists. Trends of average sire posterior means by birth-year of daughters were used to assess genetic change, and the results indicated genetic improvement of resistance to CM and KET and no genetic change for MF and RP in the NRF population.
引用
收藏
页码:3273 / 3281
页数:9
相关论文
共 27 条
[1]   Effects of trait definition on genetic parameter estimates and sire evaluation for clinical mastitis with threshold models [J].
Chang, YM ;
Gianola, D ;
Heringstad, B ;
Klemetsdal, G .
ANIMAL SCIENCE, 2004, 79 :355-363
[2]  
CHANG YM, 2002, CASE STUDIES BAYESIA, V6, P177
[3]  
FOULLEY JL, 1987, GENET SEL EVOL, V19, P197, DOI 10.1186/1297-9686-19-2-197
[4]  
GIANOLA D, 1983, GENET SEL EVOL, V15, P201, DOI 10.1186/1297-9686-15-2-201
[5]   Multivariate threshold model analysis of clinical mastitis in multiparous Norwegian dairy cattle [J].
Heringstad, B ;
Chang, YM ;
Gianola, D ;
Klemetsdal, G .
JOURNAL OF DAIRY SCIENCE, 2004, 87 (09) :3038-3046
[6]   Genetic change for clinical mastitis in Norwegian cattle: a threshold model analysis [J].
Heringstad, B ;
Rekaya, R ;
Gianola, D ;
Klemetsdal, G ;
Weigel, KA .
JOURNAL OF DAIRY SCIENCE, 2003, 86 (01) :369-375
[7]   Selection for mastitis resistance in dairy cattle: a review with focus on the situation in the Nordic countries [J].
Heringstad, B ;
Klemetsdal, G ;
Ruane, J .
LIVESTOCK PRODUCTION SCIENCE, 2000, 64 (2-3) :95-106
[8]   Genetic parameters for clinical mastitis in Holstein-Friesians in the United Kingdom: a Bayesian analysis [J].
Kadarmideen, HN ;
Rekaya, R ;
Gianola, D .
ANIMAL SCIENCE, 2001, 73 :229-240
[9]  
Lewin HA, 1999, GENETICS OF CATTLE, P163
[10]   Estimation of genetic and phenotypic parameters for clinical mastitis somatic cell production deviance, and protein yield in dairy cattle using Gibbs sampling [J].
Lund, MS ;
Jensen, J ;
Petersen, PH .
JOURNAL OF DAIRY SCIENCE, 1999, 82 (05) :1045-1051