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Individual cage housing affects feed intake and induces sex-specific effects on body weight in Japanese quails

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2024-06-03
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Reda, G. K., Ndunguru, S. F., Csernus, B. ., Lugata, J. K., Knop, R., Szabó, C., & Czeglédi, L. (2024). Individual cage housing affects feed intake and induces sex-specific effects on body weight in Japanese quails. Acta Agraria Debreceniensis, 1, 137-142. https://doi.org/10.34101/actaagrar/1/13496
Abstract

Individual cage housing in poultry production could be a potentially stressful environment for the birds that can alter feed intake, consequently induce negative effects on performance. Previous studies used individual bird-based experiments to extract the detailed molecular, physiological, and fitness outcomes of treatments. Understanding sex-specific effects of isolation on social birds such as Japanese quails (Coturnix japonica) may reveal important considerations. To understand this phenomenon, birds were kept in groups of 10 for one week and they were kept in individual cages for another week.  Daily feed intake (DFI) was measured each day and body weight was measured at the beginning, middle, and end of group rearing and at the beginning and end of individual rearing. It was found that both males and females showed a reduction DFI in response to individual rearing (p<0.0001). Females consumed on average 29.38% higher amount of feed than males. Additionally, females showed a pronounced reduction in body weight after isolation, while the effect on males was not significant. Similarly, females had on average 17.61% higher body weight than males. The body weight to DFI ratio was higher in males than females. The finding of this research revealed an important implication of isolation and sex differences.

References
  1. Abou-Kassem, D.; El-Kholy, M.; Alagawany, M.; Laudadio, V.; Tufarelli, V. (2019): Age and sex-related differences in performance, carcass traits, hemato–biochemical parameters, and meat quality in Japanese quails. Poultry Science. 98(4), 1684–1691. https://doi.org/10.3382/ps/pey543
  2. Adkins-Regan, E. (2014): Male-male sexual behavior in Japanese quail: Being “on top” reduces mating and fertilization with females. Behavioural Processes. 108, 71–79. https://doi.org/10.1016/j.beproc.2014.09.027
  3. Balthazart, J.; Schumacher, M.; Ottinger, M.A. (1983): Sexual differences in the Japanese quail: behavior, morphology, and intracellular metabolism of testosterone. General and Comparative Endocrinology. 51(2), 191–207. https://doi.org/10.1016/0016-6480(83)90072-2
  4. Bates, D.; Mächler, M.; Bolker, B.; Walker, S. (2015): Fitting Linear Mixed-Effects Models Using lme4. Journal of Statistical Software. 67(1), 1–48. https://doi.org/10.18637/jss.v067.i01
  5. Chang, G.; Liu, X.; Chang, H.; Chen, G.; Zhao, W.; Ji, D.; Chen, R.; Qin, Y.; Shi, X.; Hu, G. (2009): Behavior differentiation between wild Japanese quail, domestic quail, and their first filial generation. Poultry Science. 88(6), 1137–1142. https://doi.org/10.3382/ps.2008-00320
  6. Du Preez, J.; Sales, J. (1997): Growth rate of different sexes of the European quail (Coturnix coturnix). British poultry science. 38(3), 314–315. https://doi.org/10.1080/00071669708417994
  7. Feltenstein, M.W.; Ford, N.G.; Freeman, K.B.; Sufka, K.J. (2002): Dissociation of stress behaviors in the chick social-separation-stress procedure. Physiology & Behavior. 75(5), 675–679. https://doi.org/10.1016/S0031-9384(02)00660-1
  8. Guzmán, D.A., Kembro, J.M.; Marin, R.H. (2021): Japanese quail classified by their permanence in proximity to a high or low density of conspecifics: a search for underpinning variables. Poultry Science. 100(3), 100950. https://doi.org/10.1016/j.psj.2020.12.047
  9. Guzmán, D.A.; Pellegrini, S.; Kembro, J.M.; Marin, R.H. (2013): Social interaction of juvenile Japanese quail classified by their permanence in proximity to a high or low density of conspecifics. Poultry Science. 92(10), 2567–2575. https://doi.org/10.3382/ps.2013-03206
  10. Health, E..P.o.A.; Welfare, A.; Nielsen, S.S.; Alvarez, J.; Bicout, D.J.; Calistri, P.; Canali, E.; Drewe, J.A.; Garin‐Bastuji, B.; Gonzales Rojas, J.L.; et al. (2023): Welfare of laying hens on farm. EFSA Journal. 21(2), e07789. https://doi.org/10.2903/j.efsa.2023.7789
  11. Hiyama, G.; Mizushima, S.; Matsuzaki, M.; Tobari, Y.; Choi, J.-H.; Ono, T.; Tsudzuki, M.; Makino, S.; Tamiya, G.; Tsukahara, N. (2018): Female Japanese quail visually differentiate testosterone-dependent male attractiveness for mating preferences. Scientific Reports. 8(1), 10012. https://doi.org/10.1038/s41598-018-28368-z
  12. Horváthová, T.; Nakagawa, S.; Uller, T. (2012): Strategic female reproductive investment in response to male attractiveness in birds. Proceedings of the Royal Society B. 279(1726), 163–170. https://doi.org/10.1098/rspb.2011.0663
  13. Kaya Başar, E.; Narinç, D. (2023): Genetic Parameter Estimates of Growth Curve and Feed Efficiency Traits in Japanese Quail. Animals. 13(11), 1765. https://doi.org/10.3390/ani13111765
  14. Kuznetsova, A.; Brockhoff, P.B.; Christensen, R.H.B. (2017): LmerTest package: Tests in linear mixed effects models. Journal of Statistical Software. 82(13), 1–26. https://doi.org/10.18637/jss.v082.i13
  15. Lukanov, H.; Genchev, A.; Kolev, P. (2018): Comparative investigation of egg production in WG, GG and GL Japanese quail populations. Trakia Journal of Sciences. 4, 334–343. https://doi.org/10.15547/tjs.2018.04.011
  16. Marn, N.; Lika, K.; Augustine, S.; Goussen, B.; Ebeling, M.; Heckmann, D.; Gergs, A. (2022): Energetic basis for bird ontogeny and egg-laying applied to the bobwhite quail. Conservation Physiology. 10(1), coac063. https://doi.org/10.1093/conphys/coac063
  17. Mills, A.D.; Jones, R.B.; Faure, J.-M.; Williams, J.B. (1993): Responses to isolation in Japanese quail genetically selected for high or low sociality. Physiology & Behavior. 53(1), 183–189. https://doi.org/10.1016/0031-9384(93)90029-F
  18. NRC (National Research Council). (1994): "Nutrient Requirements of Poultry," 9th Edition/Ed. National Academy Press, Washington, D. C.
  19. Ogbonna, A.C.; Chaudhry, A.S.; Asher, L. (2022): Effect of dietary vitamin D3 and Ultraviolet B light on growth performance, blood serum parameters, gut histology, and welfare indicators of broilers. Frontiers in Animal Science. 2, 806967. https://doi.org/10.3389/fanim.2021.806967
  20. Ojelade, O.; Iyasere, O.; Durosaro, S.; Abdulraheem, I.; Akinde, A. (2022): Social isolation impairs feed intake, growth and behavioural patterns of catfish under culture conditions. Animal. 16(5), 100521. https://doi.org/10.1016/j.animal.2022.100521
  21. R Core Team. (2022): R: A language and environment for statistical computing. Version 4.2.2. R Foundation for Statistical Computing. Vienna, Austria. https://www.R-project.org/
  22. Rathert, T.Ç.; Güven, İ.; Üçkardeş, F. (2017): Sex determination of Japanese quails (Coturnix coturnix Japonica) using with zoometric measurements. Turkish Journal of Agriculture-Food Science and Technology. 5(9), 1002–1005. https://doi.org/10.24925/turjaf.v5i9.1002-1005.1278
  23. Reda, G.K.; Ndunguru, S.F.; Csernus, B.; Knop, R.; Szabó, C.; Czeglédi, L.; Lendvai, Á.Z. (under review): Dietary restriction has sexually dimorphic effect on phenotype and nutrient sensing pathway genes. Unpublished manuscript. Original research paper. Evolutionary zoology and Human Biology. University of Debrecen, Hungary.
  24. Retes, P.L.; das Neves, D.G.; Bernardes, L.F.; de Rezende Lima, D.; Ribeiro, C.B.; de Castro Gonçalves, N.; Alvarenga, R.R.; Fassani, E.J.; Zangeronimo, M.G. (2019): Reproductive characteristics of male and female Japanese quails (Coturnix coturnix japonica) fed diets with different levels of crude protein during the growth and production phases. Livestock Science. 223, 124–132. https://doi.org/10.1016/j.livsci.2019.03.011
  25. Rezvannejad, E.; Pakdel, A.; Ashtianee, S.M.; Yeganeh, H.M.; Yaghoobi, M. (2013): Analysis of growth characteristics in short-term divergently selected Japanese quail lines and their cross. Journal of Applied Poultry Research. 22(4), 663–670. https://doi.org/10.3382/japr.2011-00332
  26. Schmid, I.; Wechsler, B. (1997): Behaviour of Japanese quail (Coturnix japonica) kept in semi-natural aviaries. Applied Animal Behaviour Science. 55(1-2), 103–112. https://doi.org/10.1016/S0168-1591(97)00039-7
  27. Schweitzer, C.; Arnould, C. (2010): Emotional reactivity of Japanese quail chicks with high or low social motivation reared under unstable social conditions. Applied Animal Behaviour Science. 125(3-4), 143–150. https://doi.org/10.1016/j.applanim.2010.04.005
  28. Seiwert, C.; Adkins-Regan, E. (1998): The foam production system of the male Japanese quail: characterization of structure and function. Brain Behavior and Evolution. 52(2), 61–80. https://doi.org/10.1159/000006553
  29. Sezer, M.; Berberoglu, E.; Ulutas, Z. (2006): Genetic association between sexual maturity and weekly live-weights in laying-type Japanese quail. South African Journal of Animal Science. 36(2), 142–148. https://doi.org/10.4314/sajas.v36i2.3997
  30. Sezer, M.; Tarhan, S. (2005): Model parameters of growth curves of three meat-type lines of Japanese quail. Czech Journal of Animal Science. 50(1), 22–30. https://doi.org/10.17221/3991-CJAS
  31. Weintraub, A.; Singaravelu, J.; Bhatnagar, S. (2010): Enduring and sex-specific effects of adolescent social isolation in rats on adult stress reactivity. Brain Research. 1343, 83–92. https://doi.org/10.1016/j.brainres.2010.04.068
  32. Weldon, K.B.; Fanson, K.V.; Smith, C.L. (2016): Effects of isolation on stress responses to novel stimuli in subadult chickens (Gallus gallus). Ethology. 122(10), 818–827. https://doi.org/10.1111/eth.12529
  33. Zhang, F.; Yang, J.; Liu, L.; Yu, Y. (2022): Generalized linear–quadratic model with a change point due to a covariate threshold. Journal of Statistical Planning and Inference. 216, 194–206. https://doi.org/10.1016/j.jspi.2021.05.012