Register      Login
Animal Production Science Animal Production Science Society
Food, fibre and pharmaceuticals from animals
RESEARCH ARTICLE

Pre- and peri-pubertal feed intake: effects on age at puberty and potential litter size of replacement gilts

W. H. E. J. van Wettere A E , M. Mitchell B , D. K. Revell C and P. E. Hughes D
+ Author Affiliations
- Author Affiliations

A School of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy Campus, Roseworthy, SA 5371, Australia.

B Research Centre for Reproductive Health, The University of Adelaide, Medical School South MSN6, Frome Road, SA 5005, Australia.

C CSIRO, Division of Animal Food and Health Sciences, Floreat, WA 6014, Australia.

D Pig and Poultry Production Institute, Roseworthy Campus, Roseworthy, SA 5371, Australia.

E Corresponding author. Email: william.vanwettere@adelaide.edu.au

Animal Production Science 57(6) 1040-1046 https://doi.org/10.1071/AN15871
Submitted: 16 December 2015  Accepted: 11 March 2016   Published: 11 July 2016

Abstract

The effect of moderate restriction of pre- and peri-pubertal liveweight gain on puberty attainment and potential litter size was investigated. At 69 days of age, 48 Large White/Landrace crossbred gilts (28.3 ± 0.3 kg), were fed to attain a liveweight of 70 kg (LIGHT) or 100 kg (HEAVY) at 161 days of age (n = 24 gilts/treatment). At 161 days of age, half the gilts in each group were fed to gain liveweight at 0.5 (LOW) or 1.0 (HIGH) kg/day until puberty (n = 12 gilts/treatment). From 175 days of age, gilts received 20 min/day of full, physical boar contact. Gilts were artificially inseminated at the pubertal oestrus, with reproductive tracts collected 22 ± 0.1 days later, and the number of corpora lutea and viable embryos recorded. LIGHT-LOW gilts were older (P < 0.05) at puberty compared with LIGHT-HIGH, HEAVY-LOW and HEAVY-HIGH gilts; 207.7 ± 3.50 versus 191.7 ± 3.65, 193.1 ± 3.50 and 192.5 ± 3.65, respectively. Treatment (HIGH vs LOW) increased (P < 0.05) pubertal ovulation rate (15.2 ± 0.43 vs 13.1 ± 0.47), oestradiol at oestrus (13.4 ± 1.87 vs 9.1 ± 1.22 pg/mL) and progesterone 72 h post-oestrus (7.1 ± 0.48 vs 4.6 ± 0.50 ng/mL). Embryo number (10.8 ± 0.46) and survival (77.0 ± 3.21) were unaffected (P > 0.05) by treatment. To conclude, puberty was delayed by chronic, but not acute, dietary restriction. Although short-term, moderate increases in feed intake increased pubertal ovulation rates, embryo numbers and survival were unaffected.

Additional keywords: nutrition, pig.


References

Almeida FR, Kirkwood RN, Aherne FX, Foxcroft GR (2000) Consequences of different patterns of feed intake during the estrous cycle in gilts on subsequent fertility. Journal of Animal Science 78, 1556–1563.

Ashworth CJ, Antipatis C, Beattie L (1999) Effects of pre- and post-mating nutritional status on hepatic function, progesterone concentration, uterine protein secretion and embryo survival in Meishan pigs. Reproduction, Fertility and Development 11, 67–73.
Effects of pre- and post-mating nutritional status on hepatic function, progesterone concentration, uterine protein secretion and embryo survival in Meishan pigs.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXlsVClsA%3D%3D&md5=0caa87088406802d79188b7d5bc767a0CAS |

Beltranena E, Aherne FX, Foxcroft GR (1993) Innate variability in sexual development irrespective of body fatness in gilts. Journal of Animal Science 71, 471–480.

Booth PJ, Graigon J, Foxcroft GR (1994) Nutritional manipulation of growth and metabolic and reproductive status in prepubertal gilts. Journal of Animal Science 72, 2415–2424.

Booth PJ, Cosgrove JR, Foxcroft GR (1996) Endocrine and metabolic responses to realimentation in feed-restricted prepubertal gilts: associations among gonadotropins, metabolic hormones, glucose, and uteroovarian development. Journal of Animal Science 74, 840–848.

Ferguson EM, Slevin J, Hunter MG, Edwards SA, Ashworth CJ (2003) Effect of different nutritional regimens before ovulation on plasma concentrations of metabolic and reproductive hormones and oocyte maturation in gilts. Reproduction (Cambridge, England) 126, 61–71.
Effect of different nutritional regimens before ovulation on plasma concentrations of metabolic and reproductive hormones and oocyte maturation in gilts.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXlvFCnurw%3D&md5=59b59a965da41c90b933efaf92210a6aCAS |

Ferguson EM, Slevin J, Edwards SA, Hunter MG, Ashworth CJ (2006) Effect of alterations in the quantity and composition of the pre-mating diet on embryo survival and foetal growth in the pig. Animal Reproduction Science 96, 89–103.
Effect of alterations in the quantity and composition of the pre-mating diet on embryo survival and foetal growth in the pig.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xps1Chsr0%3D&md5=5c54cc0a3feb73c04c492a0743c9beedCAS | 16426776PubMed |

Gaughan JB, Cameron RD, Dryden GM, Young BA (1997) Effect of body composition at selection on reproductive development in large white gilts. Journal of Animal Science 75, 1764–1772.

Geisert RD, Schmitt RA (2001) Early embryonic survival in the pig: can it be improved? Journal of Animal Science 80, E54–E65.

Hunter MG, Wiesak T (1990) Evidence for and implications of follicular heterogeneity in pigs. Journal of Reproduction and Fertility Supplement 40, 163–177.

Klindt J, Yen JT, Christenson RK (2001) Effect of prepubertal feeding regimen on reproductive development and performance of gilts through the first pregnancy. Journal of Animal Science 79, 787–795.

Kummer R, Bernardi ML, Schenkel AC, Amaral Filha WS, Wentz I, Bortolozzo FP (2009) Reproductive performance of gilts with similar age but different growth rates at the onset of puberty stimulation. Reproduction in Domestic Animals 44, 255–259.
Reproductive performance of gilts with similar age but different growth rates at the onset of puberty stimulation.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1M3jsVGqsg%3D%3D&md5=99395b0a0f5b266d72e887fe2e0e87fbCAS | 18694424PubMed |

Mao J, Foxcroft GR (1998) Progesterone therapy during early pregnancy and embryonal survival in primiparous weaned sows. Journal of Animal Science 76, 1922–1928.

Miller PS, Moreno R, Johnson RK (2011) Effects of restricting energy during the gilt developmental period on growth and reproduction of lines different in lean growth rate: responses in feed intake, growth and age at puberty. Journal of Animal Science 89, 342–354.
Effects of restricting energy during the gilt developmental period on growth and reproduction of lines different in lean growth rate: responses in feed intake, growth and age at puberty.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhvFSntbg%3D&md5=0a9f22912eaba5211b8958b603979f81CAS | 20971891PubMed |

Paterson AM, Hughes PE, Pearce GP (1989) The effect of season, frequency and duration of boar contact with boars on attainment of puberty in gilts. Animal Reproduction Science 21, 115–124.
The effect of season, frequency and duration of boar contact with boars on attainment of puberty in gilts.Crossref | GoogleScholarGoogle Scholar |

Philip G, Hughes PE (1995) The effects of contact frequency and season on the efficacy of the boar effect. Animal Reproduction Science 40, 143–150.
The effects of contact frequency and season on the efficacy of the boar effect.Crossref | GoogleScholarGoogle Scholar |

Prunier A, Quesnel H (2000) Influence of the nutritional status on ovarian development in female pigs. Animal Reproduction Science 60–61, 185–197.
Influence of the nutritional status on ovarian development in female pigs.Crossref | GoogleScholarGoogle Scholar | 10844194PubMed |

Rhodes MT, Davis DL, Stevenson JS (1991) Flushing and altenogest affect litter traits in gilts. Journal of Animal Science 69, 34–40.

Ronnekleiv OK, Ojeda SR, McCann SM (1978) Undernutrition, puberty and development of estrogen positive feedback in the female rat. Biology of Reproduction 19, 414–424.
Undernutrition, puberty and development of estrogen positive feedback in the female rat.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1cXmtFaksL0%3D&md5=ede3355e3198c3a7e00d6ae418ec0ed9CAS | 719097PubMed |

Schillo KK (1992) Effects of dietary energy control on luteinising hormone secretion in cattle and sheep. Journal of Animal Science 70, 1271–1282.

Schneider JE, Wade GN (1989) Availability of metabolic fuels controls estrus cyclicity in Siberian hamsters. Science 244, 1326–1328.
Availability of metabolic fuels controls estrus cyclicity in Siberian hamsters.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXkslGnsLg%3D&md5=c12b1a792a8eba29aff36190fb35f941CAS | 2734610PubMed |

van Wettere WHEJ, Hughes PE (2007) Gilt management, oocyte quality and embryo survival. In ‘Paradigms in pig science’. (Eds J Wiseman, MA Varley, S McOrist, B Kemp) pp. 329–358. (Nottingham University Press: Nottingham)

van Wettere WHEJ, Revell DK, Mitchell M, Hughes PE (2006) Increasing the age of gilts at first boar contact improves the timing and synchrony of the pubertal response but does not affect potential litter size. Animal Reproduction Science 95, 97–106.
Increasing the age of gilts at first boar contact improves the timing and synchrony of the pubertal response but does not affect potential litter size.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD28vlt1Sjtg%3D%3D&md5=b3f8013ef212680601b84d389b6aabb8CAS |

van Wettere WHEJ, Mitchell M, Revell DK, Hughes PE (2011) Nutritional restriction of pre-pubertal liveweight gain impairs ovarian follicle growth and oocyte developmental competence of replacement gilts. Theriogenology 75, 1301–1310.
Nutritional restriction of pre-pubertal liveweight gain impairs ovarian follicle growth and oocyte developmental competence of replacement gilts.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M3ot1WmsQ%3D%3D&md5=227a24d9e0831af187919dc4ca532484CAS |

Webb R, Garnsworthy PC, Gong J-G, Armstrong DG (2004) Control of follicular growth: local interactions and nutritional influences. Journal of Animal Science 82, E63–E74.