To get insights into selection criteria for feed efficiency, 2 rabbit lines have been created: the ConsoResidual line was selected for residual feed intake (RFI) with ad libitum feeding and the ADGrestrict line was selected for ADG under restricted feeding. The aim of the present study was to evaluate the impact on carcass and meat quality of the genetic selections. This comparison was performed using 2 different feeding strategies corresponding to the selection design. Carcass and meat quality traits were recorded for the 3 lines (ConsoResidual, ADGrestrict, and an unselected control [generation 0 {G0}]) in the 2 feeding systems (ad libitum and restricted) for 163 animals. Concerning the line effect, the BW at 63 d old was higher for the ADGrestrict line compared with the G0 and ConsoResidual lines ( < 0.0001). There was no line effect on the gastrointestinal tract. The rabbits did not exhibit a different carcass yield but showed different carcass traits. Indeed, the ConsoResidual rabbits had a higher hind leg yield ( < 0.0001) but no difference in the meat-to-bone ratio of the hind leg. On the contrary, the ADGrestrict line had a higher proportion of forelegs plus thoracic cage ( = 0.03). We also found lower perirenal ( < 0.0001) and scapular fat yields ( < 0.0001) in ConsoResidual rabbits. The ADGrestrict line had an intermediate perirenal fat yield compared with the other 2 lines. The G0 line always exhibited higher fat yields. Concerning meat quality, the ConsoResidual rabbits showed a lower ultimate pH ( < 0.0001) and higher water loss (drip and cooking loss; < 0.002) compared with the G0 and ADGrestrict rabbits. The feeding level had a strong effect on the gastrointestinal tract ( = 0.0004) and the carcass yield ( = 0.001). The latter was decreased in restricted rabbits. The effects of feeding strategy on meat quality were detrimental in the case of restricted feeding. Even if the ultimate pH was slightly higher in restricted rabbits ( = 0.0002), the carcass chilling loss ( = 0.0005) and the drip loss during 6 d ( < 0.0001) were higher. The selection on ADG with restricted access to feed seems to be less adversely correlated with carcass traits and meat quality traits but it leads to an increase in the live weight of the rabbits. Adversely, the selection on RFI, without affecting growth rate, would not modify age at slaughter because growth rate is not affected, but it might induce detrimental effects on meat quality.

The aim of this preliminary experiment was to investigate the individual variability of the sexual receptivity of a rabbit doe in the presence of a buck (lordosis position, 0-1 variable). Twenty primiparous does maintained without reproduction were tested over 4 mo (3 tests per week at a 2- or 3-day interval) after their first kindling. Out of 48 tests, the receptivity rate was 52.5±50.0% on average and varied from 20.0 to 73.3% depending on the test day. The does were lactating at the beginning of the test period and a strong receptivity decrease was revealed at the peak of lactation. Receptivity did not vary according to the tester buck or to the test operator. The individual receptivity of does varied from 8.6 to 81.3%; three of them had a receptivity rate lower than 30% and four of them a receptivity rate greater than 70%. No relationship was revealed between average receptivity and body weight or body weight variations around first litter weaning. The repeatability of sexual receptivity of non-lactating does was 23.2%. Lowly receptive does had a shorter average oestrus time (<2 tests) and a longer dioestrus time (≥6 tests), whereas highly receptive does had a longer oestrus time (>4 tests) and a shorter dioestrus time (≤3 tests). The correlation between average receptivity and average oestrus time was 0.80. These results indicate a fairly high individual variability of the expression of rabbit sexual receptivity and of its duration, and justify the exploration of an eventual genetic origin in a subsequent experiment.

The success of Genome Wide Association Studies in the discovery of sequence variation linked to complex traits in humans has increased interest in high throughput SNP genotyping assays in livestock species. Primary goals are QTL detection and genomic selection. The purpose here was design of a 50-60,000 SNP chip for goats. The success of a moderate density SNP assay depends on reliable bioinformatic SNP detection procedures, the technological success rate of the SNP design, even spacing of SNPs on the genome and selection of Minor Allele Frequencies (MAF) suitable to use in diverse breeds. Through the federation of three SNP discovery projects consolidated as the International Goat Genome Consortium, we have identified approximately twelve million high quality SNP variants in the goat genome stored in a database together with their biological and technical characteristics. These SNPs were identified within and between six breeds (meat, milk and mixed): Alpine, Boer, Creole, Katjang, Saanen and Savanna, comprising a total of 97 animals. Whole genome and Reduced Representation Library sequences were aligned on >10 kb scaffolds of the de novo goat genome assembly. The 60,000 selected SNPs, evenly spaced on the goat genome, were submitted for oligo manufacturing (Illumina, Inc) and published in dbSNP along with flanking sequences and map position on goat assemblies (i.e. scaffolds and pseudo-chromosomes), sheep genome V2 and cattle UMD3.1 assembly. Ten breeds were then used to validate the SNP content and 52,295 loci could be successfully genotyped and used to generate a final cluster file. The combined strategy of using mainly whole genome Next Generation Sequencing and mapping on a contig genome assembly, complemented with Illumina design tools proved to be efficient in producing this GoatSNP50 chip. Advances in use of molecular markers are expected to accelerate goat genomic studies in coming years.

QTLs for milk SCC were detected in two dairy sheep and goat designs including 1009 AI rams and 2254 Alpine and Sanen goats sired by 20 AI sires, respectively. Animals were genotyped with the 50K ovine and caprine SNP chips. Linkage and Linkage disequilibrium analyses were performed using the QTLmap software. The high number of chromosomal regions detected tended to confirm the polygenic architecture of the mastitis resistance trait. Many of these QTLs were population specific. Hence, it is difficult to tell extent to which the genetic architecture of resistance truly differs between species and breed. High significance combined to narrow confidence intervals of a few QTLs (OAR3 in sheep) and commonalties between breeds and species (OAR11 and CHI19) might help prioritizing chromosomal regions for further fine mapping and functional characterization

Improvement of feed efficiency can be achieved by genetic selection directly on feed to BW gain ratio or for alternative traits. In the present study, 2 different traits were explored in the growing rabbit and their heritability and genetic correlations with traits recorded between weaning (30 d) and 63 d of age: i) residual feed intake (RFI), to select animals having low ad libitum feed intake independently from their production level, and ii) ADG under restricted feeding (ADGR; with a restriction level of 80% compared with ad libitum feeding of a control group), to select animals having high growth rate despite limited feed intake. To study these traits, 2 rabbit lines were established named i) ConsoResidual line and ii) ADGrestrict line. Under ad libitum or restricted feeding, it comes to select animals that waste less energy for maintenance, metabolism, or activity and retain more for tissue deposition. The selection process was similar in both lines. Data comprised records from generations 0 to 6 for about 1,800 rabbits per line measured for their BW at weaning and 63 d of age (BW63) and their individual feed consumption. Under ad libitum feeding, the heritability estimates were moderate for RFI (0.16 ± 0.05), ADG (0.19 ± 0.05), and feed conversion ratio (FCR; 0.22 ± 0.05). The high genetic correlation estimated between RFI and FCR (0.96 ± 0.03) was in accordance with the literature. The genetic correlation between RFI and ADG traits was not significant. Thus, selection for low RFI with ad libitum feeding was confirmed as a potential trait to improve FCR and reduce feed intake, with little effect on ADG. To our knowledge, there is no previous selection experiment on growing rabbits with restricted feeding. Our heritability estimates for ADGR and feed conversion ratio under restricted feeding (FCRR) were moderate (0.22 ± 0.06 and 0.23 ± 0.07, respectively) and had very high negative genetic correlation. Both selection criteria were found with high and favorable genetic correlations with feed efficiency recorded under each feeding regimen. However, their different genetic correlations with BW at weaning and at 63 d of age (BW63R; respectively, 0.85 and 0.17 for RFI and -0.25 and 0.81 for ADGR) suggested different impacts on major production traits that need further analyses to decipher the relative advantages of the 2 selection criteria, together with interactions between genotypes and feeding regimen.

Deoxyribonucleic acid (DNA) can be extracted from different tissue sources. The most common is blood, but in some situations it can be easier to take a biopsy. In some cases when it is difficult to capture animals, especially in wild populations, faeces and hairs can be considered as a source of DNA. This paper presents a pilot study conducted to compare the applicability of invasive and non-invasive sampling methods for extracting DNA for use in genetic studies of rabbits (Oryctolagus cuniculus). The study included 24 rabbits from the INRA 1001 strain. Blood, hair, ear biopsies and faeces were collected and used as DNA sources. Our aim was to verify the quantity of DNA obtained from different tissues using two or three types of extraction. DNA was obtained for all tissue types and all extraction methods.DNA extraction was shown to be optimal with the LGC (Laboratory of Cellular Genetics) blood extraction method. With regard to non-invasive methods, DNA extraction for hair using the LGC protocol and QIAamp® DNA mini kit gave very low quantities of DNA that could not be used for PCR reactions. The Chelex extraction protocol gave good results for PCR but could not be quantified. DNA extracted from faeces is a viable source of DNA for determining individual genotypes. The use of such non-invasive samples as a source of genetic material is a recent and very promising technique, especially for the study of endangered species, but these techniques are still too unreliable and costly to altogether replace invasive techniques when the latter are possible.

Gastrointestinal nematodes are one of the main health issues in sheep breeding. To identify loci affecting the resistance to Haemonchus contortus, a genome scan was carried out using 1,275 Romane × Martinik Black Belly backcross lambs. The entire population was challenged with Haemonchus contortus in 2 consecutive experimental infections, and fecal egg counts (FEC) and packed cell volumes were measured. A subgroup of 332 lambs with extreme FEC was necropsied to determine the total worm burden, length of female worms, sex ratio in the worm population, abomasal pH, and serum and mucosal G immunoglobulins (IgG) responses. Pepsinogen concentration was measured in another subset of 229 lambs. For QTL detection, 160 microsatellite markers were used as well as the Illumina OvineSNP50 BeadChip that provided 42,469 SNP markers after quality control. Linkage, association, and joint linkage and association analyses were performed with the QTLMAP software. Linkage disequilibrium (LD) was estimated within each pure breed, and association analyses were carried out either considering or not the breed origin of the haplotypes. Four QTL regions on sheep chromosomes (OAR)5, 12, 13, and 21 were identified as key players among many other QTL with small to moderate effects. A QTL on OAR21 affecting pepsinogen concentration exactly matched the pepsinogen (PGA5) locus. A 10-Mbp region affecting FEC after the 1st and 2nd infections was found on OAR12. The SNP markers outperformed microsatellites in the linkage analysis. Taking advantage of the LD helped to refine the locations of the QTL mapped on OAR5 and 13.

BACKGROUND:The genetics of transcript-level variation is an exciting field that has recently given rise to many studies. Genetical genomics studies have mainly focused on cell lines, blood cells or adipose tissues, from human clinical samples or mice inbred lines. Few eQTL studies have focused on animal tissues sampled from outbred populations to reflect natural genetic variation of gene expression levels in animals. In this work, we analyzed gene expression in a whole tissue, pig skeletal muscle sampled from individuals from a half sib F2 family shortly after slaughtering.RESULTS:QTL detection on transcriptome measurements was performed on a family structured population. The analysis identified 335 eQTLs affecting the expression of 272 transcripts. The ontologic annotation of these eQTLs revealed an over-representation of genes encoding proteins involved in processes that are expected to be induced during muscle development and metabolism, cell morphology, assembly and organization and also in stress response and apoptosis. A gene functional network approach was used to evidence existing biological relationships between all the genes whose expression levels are influenced by eQTLs. eQTLs localization revealed a significant clustered organization of about half the genes located on segments of chromosome 1, 2, 10, 13, 16, and 18. Finally, the combined expression and genetic approaches pointed to putative cis-drivers of gene expression programs in skeletal muscle as COQ4 (SSC1), LOC100513192 (SSC18) where both the gene transcription unit and the eQTL affecting its expression level were shown to be localized in the same genomic region. This suggests cis-causing genetic polymorphims affecting gene expression levels, with (e.g. COQ4) or without (e.g. LOC100513192) potential pleiotropic effects that affect the expression of other genes (cluster of trans-eQTLs).CONCLUSION:Genetic analysis of transcription levels revealed dependence among molecular phenotypes as being affected by variation at the same loci. We observed the genetic variation of molecular phenotypes in a specific situation of cellular stress thus contributing to a better description of muscle physiologic response. In turn, this suggests that large amounts of genetic variation, mediated through transcriptional networks, can drive transient cell response phenotypes and contribute to organismal adaptative potential.

Understanding the genetic structure of domestic species provides a window into the process of domestication and motivates the design of studies aimed at making links between genotype and phenotype. Rabbits exhibit exceptional phenotypic diversity, are of great commercial value, and serve as important animal models in biomedical research. Here, we provide the first comprehensive survey of nucleotide polymorphism and linkage disequilibrium (LD) within and among rabbit breeds. We resequenced 16 genomic regions in population samples of both wild and domestic rabbits and additional 35 fragments in 150 rabbits representing six commonly used breeds. Patterns of genetic variation suggest a single origin of domestication in wild populations from France, supporting historical records that place rabbit domestication in French monasteries. Levels of nucleotide diversity both within and among breeds were ~0.2%, but only 60% of the diversity present in wild populations from France was captured by domestic rabbits. Despite the recent origin of most breeds, levels of population differentiation were high (F(ST) = 17.9%), but the majority of polymorphisms were shared and thus transferable among breeds. Coalescent simulations suggest that domestication began with a small founding population of less than 1,200 individuals. Taking into account the complex demographic history of domestication with two successive bottlenecks, two loci showed deviations that were consistent with artificial selection, including GPC4, which is known to be associated with growth rates in humans. Levels of diversity were not significantly different between autosomal and X-linked loci, providing no evidence for differential contributions of males and females to the domesticated gene pool. The structure of LD differed substantially within and among breeds. Within breeds, LD extends over large genomic distances. Markers separated by 400 kb typically showed r(2) higher than 0.2, and some LD extended up to 3,200 kb. Much less LD was found among breeds. This advantageous LD structure holds great promise for reducing the interval of association in future mapping studies.

Le but du programme est de combler les deficits en marqueurs observes pour trois especes aviaires : la caille, le canard et la poule. La strategie choisie est l'obtention, a partir de plusieurs individus de lignees d'interet, de SNP (Single Nucleotide Polymorphism, polymorphisme d'un nucleotide) par une nouvelle technologie de sequencage a haut debit (sequenceur 454 GS-FLX, Roche). Nous sequencons des representations reduites du genome, en selectionnant d'une part des fragments de restriction d'ADN genomique - les memes chez tous les individus - et d'autre part les transcrits qui representent globalement la partie du genome correspondant aux genes exprimes. Ces experimentations sont realisees a partir d'echantillons d'ADN ou d'ARN issus d'individus de lignees a l'origine de croisements existants, pour chacune des trois especes. Les donnees generees par plusieurs runs de sequence seront traitees in silico : contigage a haut debit, recherche de SNP, comparaison avec les banques de sequences connues...En plus de l'interet que represente la production d'un tres grand nombre de SNP nouveaux, cette technologie devrait permettre de mieux sequencer les regions riches en (G+C) correspondant aux plus petits des microchromosomes pour lesquels il n'y a pas de sequence chez la poule. La comparaison des sequences des transcrits obtenues chez la caille et le canard avec la sequence du genome de la poule permettra d'etablir une cartographie virtuelle des SNP obtenus, grâce a la grande conservation de syntenie existant entre ces trois especes.