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1.
J Dairy Sci ; 102(11): 10564-10572, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31477289

RESUMO

The loss-of-function mutation of the apolipoprotein (APO) B gene (APOB) in Holstein cattle accounts for increased losses in calves that are homozygous for this mutation. Heterozygous carriers of the APOB mutation are clinically healthy but show decreased concentrations of plasma cholesterol and lipoproteins. So far, the metabolic effects of the mutation have only been investigated in heterozygous calves, bulls, and nonlactating females. In high-yielding dairy cows, a marked decrease in cholesterol concentration in plasma during early lactation is part of the usual metabolic changes. Given the essential role of cholesterol in fatty acid and lipid metabolism, a specific effect of the APOB mutation on metabolism and performance in dairy cows is expected. Therefore, the aim of the present study was to investigate the effects of different APOB genotypes on metabolic parameters, hepatic metabolism, and lactation and reproductive performance. Twenty pairs of full siblings with similar age, performance, and calving were investigated. Both animals of each pair were kept on the same farm and consisted of a heterozygous carrier (CDC) and a noncarrier (CDF) of the APOB mutation associated with cholesterol deficiency. Blood samples were taken in early (25.5 ± 4.7 d in milk) and mid lactation (158.2 ± 11.1 d in milk; mean ± SD), and analyzed for nonesterified fatty acids, ß-hydroxybutyrate, glucose, insulin-like growth factor-1, aspartate aminotransferase and gamma-glutamyltransferase activity, total cholesterol, free cholesterol, triacylglycerols, high density lipoprotein-cholesterol, and phospholipids. The evaluation of milk production, milk gross composition, and lactation persistency was based on official Dairy Herd Improvement Association recordings. Cholesterol and lipoprotein concentrations were lower in CDC cows than in CDF cows in early and mid lactation. Metabolic parameters, triacylglycerol concentration in plasma, and lactation and reproductive performance did not differ between CDC cows and CDF cows. The low cholesterol concentrations associated with the APOB mutation in heterozygous carriers are not because of a primary deficiency of cholesterol at a cellular level, as the term "cholesterol deficiency" suggests, but rather a consequence of reduced capacity for its transport in circulation. Overall, the data of the present study suggest that, despite the presence of the APOB mutation, cholesterol is not limiting for animals' metabolic adaptation and performance in heterozygous Holstein cows.


Assuntos
Apolipoproteínas B/genética , Bovinos/genética , Colesterol/sangue , Mutação com Perda de Função , Ácido 3-Hidroxibutírico/sangue , Animais , Transporte Biológico , Glicemia/metabolismo , Bovinos/sangue , Colesterol/deficiência , HDL-Colesterol/sangue , Ácidos Graxos não Esterificados/sangue , Feminino , Lactação , Metabolismo dos Lipídeos , Fígado/metabolismo , Leite , Reprodução , Triglicerídeos/metabolismo
2.
J Dairy Sci ; 95(11): 6770-80, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22981569

RESUMO

The objective of this research was to estimate daily genetic correlations between longitudinal body condition score (BCS) and health traits by using a random regression animal model in first-lactation Holsteins. The use of indicator traits may increase the rate of genetic progress for functional traits relative to direct selection for functional traits. Indicator traits of interest are those that are easier to record, can be measured early in life, and are strongly genetically correlated with the functional trait of interest. Several BCS records were available per cow, and only 1 record per health trait (1=affected; 0=not affected) was permitted per cow over the lactation. Two bivariate analyses were performed, the first between BCS and mastitis and the second between BCS and metabolic disease (displaced abomasum, milk fever, and ketosis). For the first analysis, 217 complete herds were analyzed, which included 28,394 BCS records for 10,715 cows and 6,816 mastitis records for 6,816 cows. For the second analysis, 350 complete herds were analyzed, which included 42,167 BCS records for 16,534 cows and 13,455 metabolic disease records for 13,455 cows. Estimation of variance components by a Bayesian approach via Gibbs sampling was performed using 400,000 samples after a burn-in of 150,000 samples. The average daily heritability (posterior standard deviation) of BCS was 0.260 (0.026) and the heritabilities of mastitis and metabolic disease were 0.020 (0.007) and 0.041 (0.012), respectively. Heritability estimates were similar to literature values. The average daily genetic correlation between BCS and mastitis was -0.730 (0.110). Cows with a low BCS during the lactation are more susceptible to mastitis, and mastitic cows are likely to have low BCS. Daily estimates of genetic correlations between BCS and mastitis were moderate to strong throughout the lactation, becoming stronger as the lactation progressed. The average daily genetic correlation between BCS and metabolic disease was -0.438 (0.125), and was consistent throughout the lactation. A lower BCS during the lactation is genetically associated with the occurrence of mastitis and metabolic disease.


Assuntos
Doenças dos Bovinos/genética , Bovinos/genética , Característica Quantitativa Herdável , Abomaso/anormalidades , Animais , Indústria de Laticínios/normas , Feminino , Nível de Saúde , Cetose/genética , Cetose/veterinária , Lactação/genética , Mastite Bovina/genética , Paresia Puerperal/genética , Gravidez
3.
Animal ; 6(4): 571-8, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22436272

RESUMO

Health traits are of paramount importance for economic dairy production. Improvement in liability to diseases has been made with better management practices, but genetic aspects of health traits have received less attention. Dairy producers in Canada have been recording eight health traits (mastitis (MAST), lameness (LAME), cystic ovarian disease (COD), left displaced abomasum (LDA), ketosis (KET), metritis (MET), milk fever (MF) and retained placenta (RP)) since April 2007. Genetic analyses of these traits were carried out in this study for the Holstein breed. Edits on herd distributions of recorded diseases were applied to the data to ensure a sufficient quality of recording. Traits were analysed either individually (MAST, LAME, COD) or were grouped according to biological similarities (LDA and KET, and MET, MF and RP) and analysed with multiple-trait models. Data included 46 104 cases of any of the above diseases. Incidence ranged from 2.3% for MF to 9.7% for MAST. MET and KET also had an incidence below 4.0%. Variance components were estimated using four different sire threshold models. The differences between models resulted from the inclusion of days at risk (DAR) and a cow effect, in addition to herd, parity and sire effects. Models were compared using mean squared error statistic. Mean squared error favoured, in general, the sire and cow within sire model with regression on DAR included. Heritabilities on the liability scale were between 0.02 (MET) and 0.21 (LDA). There was a moderate, positive genetic correlation between LDA and KET (0.58), and between MET and RP (0.79).


Assuntos
Doenças dos Bovinos/genética , Bovinos/genética , Característica Quantitativa Herdável , Abomaso/anormalidades , Criação de Animais Domésticos/métodos , Animais , Canadá , Endometrite/genética , Endometrite/veterinária , Feminino , Cetose/genética , Cetose/veterinária , Coxeadura Animal/genética , Mastite Bovina/genética , Modelos Genéticos , Cistos Ovarianos/genética , Cistos Ovarianos/veterinária , Paresia Puerperal/genética , Placenta Retida/genética , Placenta Retida/veterinária , Gravidez
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