Genetic selection for bovine chromosome 18 haplotypes associated with divergent somatic cell score affects postpartum reproductive and metabolic performance.


Journal

Journal of dairy science
ISSN: 1525-3198
Titre abrégé: J Dairy Sci
Pays: United States
ID NLM: 2985126R

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 15 12 2018
accepted: 15 07 2019
pubmed: 16 9 2019
medline: 1 1 2020
entrez: 16 9 2019
Statut: ppublish

Résumé

The susceptibility of animals to periparturient diseases has a great effect on the economic efficiency of dairy industries, on the frequency of antibiotic treatment, and on animal welfare. The use of selection for breeding cows with reduced susceptibility to diseases offers a sustainable tool to improve dairy cattle farming. Several studies have focused on the association of distinct bovine chromosome 18 genotypes or haplotypes with performance traits. The aim of this study was to test whether selection of Holstein Friesian heifers via SNP genotyping for alternative paternal chromosome 18 haplotypes associated with favorable (Q) or unfavorable (q) somatic cell scores influences postpartum reproductive and metabolic diseases. Thirty-six heifers (18 Q and 18 q) were monitored from 3 wk before calving until necropsy on d 39 (± 4 d) after calving. Health status and rectal temperature were measured daily, and body condition score and body weight were assessed once per week. Blood samples were drawn twice weekly, and levels of insulin, nonesterified fatty acids, insulin-like growth factor-I, growth hormone, and β-hydroxybutyrate were measured. Comparisons between the groups were performed using Fisher's exact test, chi-squared test, and the GLIMMIX procedure in SAS. Results showed that Q-heifers had reduced incidence of metritis compared with q-heifers and were less likely to develop fever. Serum concentrations of β-hydroxybutyrate were lower and insulin-like growth factor-I plasma concentrations were higher in Q- compared with q-heifers. However, the body condition score and withers height were comparable between haplotypes, but weight loss tended to be lower in Q-heifers compared with q-heifers. No differences between the groups were detected concerning retained fetal membranes, uterine involution, or onset of cyclicity. In conclusion, selection of chromosome 18 haplotypes associated with a reduced somatic cell score resulted in a decreased incidence of postpartum reproductive and metabolic diseases in this study. The presented data add to the existing knowledge aimed at avoiding negative consequences of genetic selection strategies in dairy cattle farming. The underlying causal mechanisms modulated by haplotypes in the targeted genomic region and immune competence necessitate further investigation.

Identifiants

pubmed: 31521359
pii: S0022-0302(19)30793-3
doi: 10.3168/jds.2018-16171
pii:
doi:

Substances chimiques

Fatty Acids, Nonesterified 0
Insulin 0
Growth Hormone 9002-72-6
3-Hydroxybutyric Acid TZP1275679

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9983-9994

Informations de copyright

The Authors. Published by FASS Inc. and Elsevier Inc. on behalf of the American Dairy Science Association®. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Auteurs

M M Meyerholz (MM)

Clinic for Ruminants with Ambulatory and Herd Health Services, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, 85764 Oberschleißheim, Germany; Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany. Electronic address: marie.meyerholz@lmu.de.

L Rohmeier (L)

Clinic for Ruminants with Ambulatory and Herd Health Services, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, 85764 Oberschleißheim, Germany; Clinic for Swine, Small Ruminants, Forensic Medicine and Ambulatory Service, University of Veterinary Medicine, 30173 Hannover, Germany.

T Eickhoff (T)

Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany.

A Hülsebusch (A)

Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany.

S Jander (S)

Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany.

M Linden (M)

Faculty of Mathematics and Physics, Leibniz University, 30167 Hannover, Germany.

L Macias (L)

Clinic for Ruminants with Ambulatory and Herd Health Services, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, 85764 Oberschleißheim, Germany.

M Koy (M)

Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany; Clinic for Poultry, University of Veterinary Medicine, 30559 Hannover, Germany.

A Heimes (A)

Leibniz Institute for Farm Animal Biology, Genome Biology, 18196 Dummerstorf, Germany.

L Gorríz-Martín (L)

Clinic for Cattle, University of Veterinary Medicine, 30173 Hannover, Germany.

D Segelke (D)

Vereinigte Informationssysteme Tierhaltung w.V. (VIT) Verden, 27283 Verden (Aller), Germany.

S Engelmann (S)

Institute for Microbiology, Technical University, 38106 Braunschweig, Germany; Microbial Proteomics, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.

M Schmicke (M)

Clinic for Cattle, University of Veterinary Medicine, 30173 Hannover, Germany.

M Hoedemaker (M)

Clinic for Cattle, University of Veterinary Medicine, 30173 Hannover, Germany.

W Petzl (W)

Clinic for Ruminants with Ambulatory and Herd Health Services, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, 85764 Oberschleißheim, Germany.

H Zerbe (H)

Clinic for Ruminants with Ambulatory and Herd Health Services, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, 85764 Oberschleißheim, Germany.

H-J Schuberth (HJ)

Immunology Unit, University of Veterinary Medicine, 30559 Hannover, Germany.

Ch Kühn (C)

Leibniz Institute for Farm Animal Biology, Genome Biology, 18196 Dummerstorf, Germany; Agricultural and Environmental Faculty, University Rostock, 18059 Rostock, Germany.

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Classifications MeSH