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, Richardson RI: Shelf life and quality of pork and pork products with raised n-3 PUFA. Meat Sci 2000, 55 : 213-221. 30. Kouba M, Enser M, Whittington F, Nute GR, Wood JD: Effect of a high-linoleic acid diet on lipogenic enzyme activities, fatty acid composition, and meat quality in the growing pig. J Anim Sci 2003, 81: 1967-1979. 31. Fontanillas R, Barroeta A, Baucells MD, Guardiola F: Backfat fatty acid evolution in swine fed diets high in either cis-monounsaturated, trans, or (n-3) fats. J Anim Sci 1998, 76: 1045-1055. 32. Enser M, Richardson RI, Wood JD, Gill BP, Sheard

linoleic acids alter adipose tissue and milk lipids of pregnant and lactating sows. J. Nutr., 130 (9): 2292-2298. Bolton-Smith C., Woodward M., Smith W. C. S., Tunstall-Pedoe H. (1991). Dietary and non dietary predictors of serum total HDL cholesterol in men and women: results from the Scottish Heart Health Study. Int. J. Epidemiol., 20, 95-104. Grześkowiak E., Borzuta K., Tratwal Z. (2002). Effect of feeding pigs with concentrates supplemented with linseeds on fatty acid profile in backfat. Ann. Anim. Sci. Suppl., 2: 289-292. Hoffman L. C., Kroucamp M., Manley M. (2007

Abstract

The aim of this study was to verify the hypothesis that carcass traits, quality and oxidative stability of meat, and fatty acids profile in intramuscular fat (IMF) of M. longissimus lumborum et thoracis (MLLT) and backfat (BF) are different between the observed genotypes of pigs. A total of 64 animals were included in the experiment, 32 pigs of native breed Prestice Black-Pied breed (PBP) and 32 pigs of hybrid combination Large White × Landrace sows × Duroc × Pietrain boars (LWLDP). PBP pigs showed higher values of IMF (P≤0.01) and BF, lower lean meat content and drip loss value (P≤0.001) than the LWLDP hybrid. The value of pH45,24 was higher (P≤0.05) in PBP pigs. The analysis of fatty acid profile in MLLT showed higher content of C8:0 (P≤0.01), C10:0 (P≤0.01), C15:0 (P≤0.01), C22:0 (P≤0.05), C18:1 n-9 (P≤0.01), C18:3 n-6 (P≤0.001), C20:3 n-3 (P≤0.05), C20:4 n-6 (P≤0.01), C22:4 n-6 (P≤0.05), C22:5 n-3 (P≤0.01) and C22:6 n-3 (P≤0.01) in LWLDP than in PBP pigs. The opposite trend was observed in C18:1 n-9 (P≤0.01) and C20:5 n-3 (P≤0.01). Higher content of MUFA as well as the MUFA/SFA ratio were found in PBP breed (P≤0.01). Higher levels of C10:0 (P≤0.01), C12:0 (P≤0.01), C14:0 (P≤0.001), C16:0 (P≤0.001), C14:1 n-5 (P≤0.01), C16:1 n-7 (P≤0.05), C18:1 n-7 (P≤0.001), C20:5 n-3 (P≤0.01) and C22:6 n-3 (P≤0.05) in BF were found in LWLDP pigs, however the content of C24:1 n-9 (P≤0.01), C18:2 n-6 (P≤0.05), C18: n-3 (P≤0.05), C20:4 n-6 (P≤0.01) and C22:5 n-3 (P≤0.01) was higher in PBP pigs. SFA content was higher (P≤0.001) in LWLDP hybrid, but PUFA (P≤0.01), n-6 PUFA (P≤0.05) and mainly n-3 PUFA (P≤0.01) were higher in PBP pigs. In BF, the MUFA/SFA (P≤0.05) and PUFA/SFA (P≤0.001) ratios were higher in PBP pigs; on the contrary the MUFA/PUFA (P≤0.05) ratio was higher in LWLDP pigs.

Abstract

The objective of the study was to identify the impact of selection on genetic resistance against scrapie disease related to lamb growth performance attributes for Suffolk, Kent, Charollais, and Texel lambs.The allelic genotypes were grouped according to the presence of scrapie resistant allele (ARR): ARR homozygotes, ARR heterozygotes, no presence of ARR allele. The influence of these groups on lamb live weight (LW), musculus longissimus lumborum et thoracis depth (MLLT), and back-fat thickness at 100 days of age was investigated using SAS software. No significant differences for Suffolk and Charollais breeds were detected. Significantly highest LW (34.41 kg) and MLLT (27.80 mm) were noticed for Kent ARR homozygotes lambs, while significantly lowest values were estimated at lambs with absent ARR allele (LW = 33.42 kg, MLLT = 26.68 mm). Significantly lower muscle depth (–0.69 mm) was detected for Texel ARR homozygote compared to ARR heterozygote lambs. As a result, we were unable to detect a consistent evidence for reduced growth performance traits in relation to genetic resistance against scrapie disease. However, the number of animals in some groups caused as a limiting factor. This can be a potential reason of opposed trends in Texel and Kent lambs.

composition of backfat and intramuscular fat. Meat Sci., 93: 507–516. Brzóska F., Śliwinski B., Michalik-Rutkowska O. (2010). Rapeseed-based feeds and their contribution to the national protein supply and nutritional value (in Polish). Part 1. Wiad. Zoot., 48: 11–18. Chen C.C., Chiou P.W.S., Yu B. (2010). Evaluating nutritional quality of single stage- and two stage-fermented soybean meal. Asian-Australas. J. Anim. Sci., 23: 598–606. Choct M., Dersjant -Li Y., McLeish J., Peisker M. (2010). Soy oligosaccharides and soluble non-starch polysaccharides: a review of digestion

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carcasses by Ultra-Fom 300 and CGMdevices (in Polish). Ann. of Meat and Fat Res. Inst., XLI, pp. 95-108. Fox J.B. (1980). Diffusion of chloride nitrite and nitrate in beef and pork. J. Food Sci., 45: 177-178. Grześkowiak E., Borys A., Borzuta K., Buczyński J.T., Lisiak D. (2009). Slaughter value, meat quality and backfat fatty acid profile in Złotnicka White and Złotnicka Spotted fatteners. Anim. Sci. Pap. Rep., 2: 115-125. Grześkowiak E., Borzuta K., Lisiak D., Strzelecki J., Janiszewski P. (2010). Physical-chemical and sensory properties, as well as composition of fatty

DGAT1 toaregion of chromosome 4 that contains QTLfor growth and fatness. Anim. Genet., 33: 472-473. Rekiel A., Więcek J., Beyga K. (2011). Analysis of the relationship between fatness of late pregnant and lactating sows and selected lipid parameters of blood, colostrum and milk. Ann. Anim. Sci., 11: 487-495. Rekiel A., Więcek J., Kuczyńska B., Bartosik J., Warda A., Furman K. (2015). Effect of the backfat thickness at point P2 during insemination on the selected parameters of colostrum and milk of the sows. Ann. Warsaw Univ. Live Sci. - SGGW Anim. Sci., 54: 153