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Early development and reproductive lifespan of rabbit females: implications of growth rate, rearing diet and body condition at first mating

Published online by Cambridge University Press:  20 February 2018

E. Martínez-Paredes ,
L. Ródenas ,
J. J. Pascual  and
D. Savietto
E. Martínez-Paredes
Affiliation:
Instituto de Ciencia y Tecnología Animal, Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain
L. Ródenas
Affiliation:
Instituto de Ciencia y Tecnología Animal, Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain
J. J. Pascual
Affiliation:
Instituto de Ciencia y Tecnología Animal, Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain
D. Savietto*
Affiliation:
GenPhySE, Université de Toulouse, INRA, ENVT, 31326 Castanet Tolosan, France
*
†E-mail: [email protected]
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Abstract

Factors influencing early development such as birth weight, nest competition, and the diet received during rearing have been proposed as elements conditioning the future reproductive performance of European rabbit (Oryctolagus cuniculus) females. To evaluate their effects, we followed the life of 1513 females from birth to time of death, culling or censoring (animals alive at a fixed date). Between 0 and 63 days of age 353 females died. From the remaining 1160 females, 864 were chosen based on their birth weight to be transferred from the selection to the production farm. At this farm, 431 females received the control diet (184 g of CP, 381 g of NDF and 11.8 MJ of DE per kg DM), while the other 433 received the fibrous diet (134 g of CP, 436 g of NDF and 10.0 MJ of DE per kg DM). Throughout the rearing period, we checked for the individual live weight and body condition (perirenal fat thickness) at first artificial insemination. Reproductive lifespan was defined as the number of days between the first parturition and the time of death, culling or censoring. Birth weight affected the survival of newborn females during lactation and the presence of a milk spot at birth (related to nest competition) increased the survivability of newborns weighing <45 g (P<0.001). Rearing diet altered the growth curve of females and their body condition at first insemination. The diet also altered the relative risk of death during the rearing period, which was lower among females fed on the fibrous diet (−12.5%; P<0.001). Therefore, a higher number of females fed with this diet reached their reproductive life, directly affecting the productivity measured per housed female. Fatter females at first insemination had smaller litter sizes and a higher risk of being culled than lean ones (P<0.05). In general, the fibrous diet reduced the risk of leaving the herd at early rearing, and both birth weight and perirenal fat thickness affected female’s reproductive lifespan. An excess of fat (positive change in one unit of perirenal fat) at their first insemination represented an increased the risk of death or elimination of 13%.

Keywords

Oryctolagus cuniculusbirth weightnutritionreproductionsurvival
Type
Research Article
Information
animal , Volume 12 , Issue 11 , November 2018 , pp. 2347 - 2355
Copyright
© The Animal Consortium 2018 

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References

Argente, M, Santacreu, MA, Climent, A and Blasco, A 1999. Phenotypic and genetic parameters of birth weight and weaning weight of rabbits born from unilaterally ovariectomized and intact does. Livestock Production Science 57, 159–167.Google Scholar
Arias-Álvarez, M, García-García, RM, Rebollar, PG, Nicodemus, N, Revuelta, L, Millán, P and Lorenzo, PL 2009. Effects of a lignin-rich fibre diet on productive, reproductive and endocrine parameters in nulliparous rabbit does. Livestock Science 123, 107–115.Google Scholar
Bautista, A, Zepeda, JA, Reyes-Meza, V, Martínez-Gómez, M, Rödel, HG and Hudson, R 2015. Contribution of within-litter interactions to individual differences in early postnatal growth in the domestic rabbit. Animal Behaviour 108, 145–153.Google Scholar
Coureaud, G, Fortun-Lamothe, L, Langlois, D and Schaal, B 2007. The reactivity of neonatal rabbits to the mammaty pheromone as a probe for viability. Animal 1, 1026–1032.Google Scholar
Coureaud, G, Schaal, B, Coudert, P, Rideaud, P, Fortun-Lamothe, L, Hudson, R and Orgeur, P 2000. Immediate postnatal sucking in the rabbit: its influence on pup survival and growth. Reproduction Nutrition and Development 40, 19–32.Google Scholar
De Blas, C and Mateos, GG 2010. Feed formulation. In Nutrition of the rabbit (ed. C De Blas and J Wiseman), pp 222–232. CABI Publishing, Wallingford, UK.Google Scholar
Drummond, H, Vázquez, E and Sánchez-Colón, S 2000. Competition for milk in the domestic rabbits: survivors benefit from littermate deaths. Ethology 106, 511–526.Google Scholar
Fontana, L, Partridge, L and Longo, VD 2010. Extending healthy life span: from yeast to humans. Science 328, 321–326.Google Scholar
Fortun-Lamothe, L, Prunier, A, Bolet, G and Lebas, F 1999. Physiological mechanisms involved in the effects of concurrent pregnancy and lactation on foetal growth and mortality in the rabbit. Livestock Production Science 60, 229–241.Google Scholar
Fox, J 2002. Cox proportional hazard regression for survival data. Appendix to an R and S-Plus companion to applied regression. In An R and S-plus companion to applied regression (ed. J Fox), pp 1–18. Sage Publications, Inc, London, UK.Google Scholar
García-Torres, E, Hudson, R, Castelán, F, Martínez-Gómez, M and Bautista, A 2015. Differential metabolism of brown adipose tissue in newborn rabbits in relation to position in the litter huddle. Journal of Thermal Biology 51, 33–41.Google Scholar
Gidenne, T 2015. Dietary fibres in the nutrition of the growing rabbit and recommendations to preserve digestive health: a review. Animal 9, 227–242.Google Scholar
Hardman, MJ, Hull, D and Oyesiku, J 1970. The influence of birth weight and nutrition on postnatal growth of rabbits. Neonatology 16, 306–312.Google Scholar
Jilge, B, Kuhnt, B, Landerer, W and Rest, S 2001. Circadian temperature rhythms in rabbit pups and in their does. Laboratory animals 35, 364–373.Google Scholar
Martínez-Paredes, E, Ródenas, L, Martínez-Vallespín, B, Cervera, C, Blas, E, Brecchia, G, Boiti, C and Pascual, JJ 2012. Effects of feeding programme on the performance and energy balance of nulliparous rabbit does. Animal 6, 1086–1095.Google Scholar
O’Downd, S, Hoste, S, Mercer, JT, Fowler, VR and Edwards, SA 1997. Nutritional modification of body composition and the consequences for reproductive performance and longevity in genetically lean sows. Livestock Production Science 52, 155–165.Google Scholar
Pascual, JJ, Blanco, J, Piquer, O, Quevedo, F and Cervera, C 2004. Ultrasound measurements of perirenal fat thickness to estimate the body condition of reproducing rabbit does in different physiological states. World Rabbit Science 12, 7–21.Google Scholar
Pascual, JJ, Cervera, C and Fernández-Carmona, J 2002a. A feeding programme for young rabbit does based on lucerne. World Rabbit Science 10, 7–13.Google Scholar
Pascual, JJ, Motta, W, Cervera, C, Quevedo, F, Blas, E and Fernández-Carmona, J 2002b. Effect of dietary energy source on the performance and perirenal fat thickness evolution of primiparous rabbit does. Animal Science 75, 267–279.Google Scholar
Pascual, JJ, Savietto, D, Cervera, C and Baselga, M 2013. Resources allocation in reproductive rabbit does: a review of feeding and genetic strategies for suitable performances. World Rabbit Science 21, 123–144.Google Scholar
Poigner, J, Szendrö, Z, Lévai, A, Radnai, I and Biró-Németh, E 2000. Effect of birth weight and litter size at suckling age on reproductive performance in does as adults. World Rabbit Science 8, 103–109.Google Scholar
Quevedo, F, Cervera, C, Blas, E, Baselga, M, Costa, C and Pascual, JJ 2005. Effect of selection for litter size and feeding programme on the performance of young rabbit females during rearing and first pregnancy. Animal Science 80, 161–168.Google Scholar
R Core Team 2016. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Retrieved on 10 December 2016, from http://www.R-project.org.Google Scholar
Rommers, JM, Meijerhof, R, Noordhuizen, JPTM and Kemp, B 2004a. Effect of feeding program during rearing and age at first insemination on performances during subsequent reproduction in young rabbit does. Reproduction Nutrition and Development 44, 321–332.Google Scholar
Rommers, JM, Meijerhof, R, Noordhuizen, JPTM and Kemp, B 2004b. The effect of level of feeding in early gestation on reproductive success in young rabbit does. Animal Reproduction Science 81, 151–158.Google Scholar
Rosell, JM and de la Fuente, LF 2009. Culling and mortality in breeding rabbits. Preventive Veterinary Medicine 88, 120–127.Google Scholar
Ross, MH 1972. Length of life and caloric restriction. The American Journal of Clinical Nutrition 25, 834–834.Google Scholar
Savietto, D, Marono, S, Martínez, I, Martínez-Paredes, E, Ródenas, L, Cervera, C and Pascual, JJ 2016. Patterns of body condition use and its impact on fertility. World Rabbit Science 24, 39–45.Google Scholar
Sonnenburg, ED, Smits, SA, Tikhonov, M, Higginbottom, SK, Wingreen, NS and Sonnenburg, JL 2016. Diet-induced extinctions in the gut microbiota compound over generations. Nature 529, 212–215.Google Scholar
Szendrö, Zs, Gyovai, M, Maertens, L, Biró-Németh, E, Radnai, I, Matics, Zs, Princz, Z, Gerencser, Zs and Horn, P 2006. Influence of birth weight and nutrient supply before and after weaning on the performance of rabbit does to age of the first mating. Livestock Science 103, 54–64.Google Scholar
Tamburini, S, Shen, N, Wu, HC and Clemente, JC 2016. The microbiome in early life: implications for health outcomes. Nature Medicine 22, 713–722.Google Scholar
Tarrés, J, Tibau, J, Piedrafita, J, Fábrega, E and Reixach, J 2006. Factors affecting longevity in maternal Duroc swine lines. Livestock Science 100, 121–131.Google Scholar
Theilgaard, P, Sánchez, JP, Pascual, JJ, Friggens, NC and Baselga, M 2006. Effect of body fatness and selection for prolificacy on survival of rabbit does assessed using a cryopreserved control population. Livestock Science 103, 65–73.Google Scholar
Vicente, JS, Llobat, L, Viudes-de-Castro, MP, Lavara, R, Baselga, M and Marco-Jiménez, F 2012. Gestational losses in a rabbit line selected for growth rate. Theriogenology 77, 81–88.Google Scholar
Villamide, MJ, Carabaño, R, Maertens, L, Pascual, JJ, Gidenne, T, Falcao-e-Cunha, L and Xiccato, G 2009. Prediction of the nutritional value of European compound feeds for rabbits by chemical components and in vitro analysis. Animal Feed Science and Technology 150, 283–294.Google Scholar
Wells, K, O’Hara, RB, Cooke, BD, Mutze, GJ, Prowse, TA and Fordham, DA 2016. Environmental effects and individual body condition drive seasonal fecundity of rabbits: identifying acute and lagged processes. Oecologia 181, 853–864.Google Scholar
Xiccato, G, Bernardini, M, Castellini, C, Dalle Zotte, A, Queaque, PI and Trocino, A 1999. Effect of postweaning feeding on the performance and energy balance of female rabbits at different physiological states. Journal of Animal Science 77, 416–426.Google Scholar
Xiccato, G, Parigi-Bini, R, Dalle Zotte, A, Carazzolo, A and Cossu, ME 1995. Effect of dietary energy level, addition of fat and physiological state on performance and energy balance of lactating and pregnant rabbit does. Animal Science 61, 387–398.Google Scholar
Xiccato, G and Trocino, A 2010. Energy and protein metabolism and requirements. In Nutrition of the Rabbit (ed. C De Blas and J Wiseman), pp 83–118. CABI Publishing, Wallingford, UK.Google Scholar
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