• This record comes from PubMed

Combined Effect of Dietary Protein, Ractopamine, and Immunocastration on Boar Taint Compounds, and Using Testicle Parameters as an Indicator of Success

. 2020 Nov 14 ; 9 (11) : . [epub] 20201114

Status PubMed-not-MEDLINE Language English Country Switzerland Media electronic

Document type Journal Article

Grant support
not available South African Pork Producers' Organisation
84633 South African Research Chairs in Meat Science Initiative

This study investigates the combined effect of immunocastration, dietary protein level (low, medium or high) and ractopamine hydrochloride supplementation (0 or 10 mg/kg) on the adipose concentrations of androstenone, skatole and indole in pigs, and explores whether body mass, carcass fatness or testicular parameters may be indicators of boar taint in these carcasses. Immunocastration was successful in decreasing testicle functioning, and adipose androstenone and skatole concentrations, in all individuals. Immunocastration decreased testicle weight and length, seminiferous tubule circumference and epithelium thickness. Testicle tissue from immunocastrates was also paler, and less red in color, in comparison to non-castrated controls. Dietary protein level and ractopamine hydrochloride supplementation had no influence on the adipose concentration of androstenone, skatole and indole. Testicle size and color were moderate to strong indicators of androstenone and skatole concentrations in the carcasses, and thus vaccination success. Immunocastration together with the adjustment of dietary protein and ractopamine hydrochloride supplementation, is successful in preventing boar taint while maintaining growth performance.

See more in PubMed

Patterson R.L.S. 5a-Androst-16-ene-3-one: Compound responsible for taint in boar fat. J. Sci. Food Agric. 1968;19:31–37. doi: 10.1002/jsfa.2740190107. DOI

Vold E. Fleischproduktionseigenschaften bei Ebern und Kastraten. IV. Organoleptische und Gaschromatographische Untersuchungen Wasserdampfflüchtiger Stoffe des Rückenspeckes von Ebern. Meld. Nor. Landbrukshogsk. 1970;49:1–25.

Bonneau M. Compounds responsible for boar taint, with special emphasis on androstenone: A review. Livest. Prod. Sci. 1982;9:687–705. doi: 10.1016/0301-6226(82)90017-3. DOI

Garcia-Regueiro J.A., Diaz I. Evaluation of the contribution of skatole, indole, androstenone and androstenols to boar-taint in back fat of pigs by HPLC and capillary gas chromatography (CGC) Meat Sci. 1989;25:307–316. doi: 10.1016/0309-1740(89)90048-X. PubMed DOI

Rault J.L., Lay D.C., Jr., Marchant-Fordel J.N. Castration induced pain in pigs and other livestock. Appl. Anim. Behav. Sci. 2011;135:214–225. doi: 10.1016/j.applanim.2011.10.017. DOI

Needham T., van Zyl K., Hoffman L.C. Correlations between PORCUS classification and androstenone in boars, and effects of cooking methods thereon. S. Afr. J. Anim. Sci. 2020;50:120–128. doi: 10.4314/sajas.v50i1.13. DOI

Fuchs T., Nathues H., Koehrmann A., Andrews S., Brock F., Sudhaus N., Klein G., Beilage E.G. A comparison of the carcase characteristics of pigs immunized with a ‘gonadotrophin-releasing factor (GnRF)’ vaccine against boar taint with physically castrated pigs. Meat Sci. 2009;83:702–705. doi: 10.1016/j.meatsci.2009.08.007. PubMed DOI

Font-i-Furnols M., Gispert M., Diestre A., Oliver M.A. Acceptability of boar meat by consumers depending on their age, gender, culinary habits, sensitivity and appreciation of androstenone smell. Meat Sci. 2003;64:433–440. doi: 10.1016/S0309-1740(02)00212-7. PubMed DOI

Bonneau M., Denmat M., Vaudelet C., Veloso-Nunes J.R., Mortensen A.B., Mortensen H.P. Contribution of fat androstenone and skatole to boar taint I. Sensory attributes of fat and pork meat. Livest. Prod. Sci. 1992;32:63–80. doi: 10.1016/S0301-6226(12)80012-1. DOI

Font-i-Furnols M. Consumer studies on sensory acceptability of boar taint: A review. Meat Sci. 2012;92:319–329. doi: 10.1016/j.meatsci.2012.05.009. PubMed DOI

Keller A., Zhuang H., Chi Q., Vosshall L.B., Matsunami H. Genetic variation in a human odorant receptor alters odour perception. Nature. 2007;449:468–472. doi: 10.1038/nature06162. PubMed DOI

De Kock H.L., van Heerden S.M., Heinze P.H., Dijksterhuis B.B., Minnaar A. Reaction to boar odour by different South African consumer groups. Meat Sci. 2001;59:353–362. doi: 10.1016/S0309-1740(01)00087-0. PubMed DOI

Gilbert A.N., Wysocki C.J. Results of the smell survey. Natl. Geogr. 1987;172:514–525.

Annor-Frempong I.E., Nute G.R., Whittington F.W., Wood J.D. The problem of taint in pork: 1. Detection thresholds and odour profiles of androstenone and skatole in a model system. Meat Sci. 1997;46:45–55. doi: 10.1016/S0309-1740(97)00003-X. PubMed DOI

Wysocki C.J., Dorries K.M., Beauchamp G.K. Ability to perceive androstenone can be acquired by ostensibly anosmic people. Proc. Natl. Acad. Sci. USA. 1989;86:7976–7978. doi: 10.1073/pnas.86.20.7976. PubMed DOI PMC

Bonneau M., Weiler U. Pros and Cons of Alternatives to Piglet Castration: Welfare, Boar Taint, and Other Meat Quality Traits. Animals. 2019;9:884. doi: 10.3390/ani9110884. PubMed DOI PMC

Zamaratskaia G., Gilmore W.J., Lundström K., Squires E.J. Effect of testicular steroids on catalytic activities of cytochrome P450 enzymes in porcine liver microsomes. Food Chem. Toxicol. 2007;45:676–681. doi: 10.1016/j.fct.2006.10.023. PubMed DOI

Font-i-Furnols M., Martín-Bernal R., Aluwé M., Bonneau M., Haugen J.-E., Mörlein D., Mörlein J., Panella-Riera N., Škrlep M. Feasibility of on/at Line Methods to Determine Boar Taint and Boar Taint Compounds: An Overview. Animals. 2020;10:1886. doi: 10.3390/ani10101886. PubMed DOI PMC

Squires E.J., Bone C., Cameron J. Pork Production with Entire Males: Directions for Control of Boar Taint. Animals. 2020;10:1665. doi: 10.3390/ani10091665. PubMed DOI PMC

Needham T., Lambrechts H., Hoffman L. Castration of male livestock and the potential of immunocastration to improve animal welfare and production traits: Invited Review. S. Afr. J. Anim. Sci. 2017;47:731–742. doi: 10.4314/sajas.v47i6.1. DOI

Škrlep M., Tomašević I., Mörlein D., Novaković S., Egea M., Garrido M.D., Linares M.B., Peñaranda I., Aluwé M., Font-i-Furnols M. The Use of Pork from Entire Male and Immunocastrated Pigs for Meat Products—An Overview with Recommendations. Animals. 2020;10:1754. doi: 10.3390/ani10101754. PubMed DOI PMC

Needham T., Hoffman L.C., Gous R. Growth responses of entire and immunocastrated male pigs to dietary protein with and without ractopamine hydrochloride. Animal. 2017;11:1482–1487. doi: 10.1017/S1751731117000271. PubMed DOI

Needham T., Hoffman L.C. Carcass traits and cutting yields of entire and immunocastrated pigs fed increasing protein levels with and without ractopamine hydrochloride supplementation. J. Anim. Sci. 2015;93:4545–4556. doi: 10.2527/jas.2015-9183. PubMed DOI

Needham T., Hoffman L.C. Physical meat quality and chemical composition of the Longissimus thoracis of entire and immunocastrated pigs fed varying dietary protein levels with and without ractopamine hydrochloride. Meat Sci. 2015;110:101–108. doi: 10.1016/j.meatsci.2015.06.017. PubMed DOI

Lealiifano A., Pluske J.R., Nicholls R., Dunshea F., Campbell R., Hennessy D., Miller D., Hansen C.F., Mullan B. Reducing the length of time between slaughter and the secondary gonadotropin-releasing factor immunization improves growth performance and clears boar taint compounds in male finishing pigs. J. Anim. Sci. 2011;89:2782–2792. doi: 10.2527/jas.2010-3267. PubMed DOI

Verheyden K., Noppe H., Aluwé M., Millet S., Vanden Bussche J., De Brabander H. Development and validation of a method for simultaneous analysis of the boar taint compounds indole, skatole and androstenone in pig fat using liquid chromatography-multiple mass spectrometry. J. Chromatogr. A. 2007;1174:132–137. doi: 10.1016/j.chroma.2007.08.075. PubMed DOI

Kubale V., Batorek N., Škrlep M., Prunier A., Bonneau M., Fazarinc G., Čandek-Potokar M. Steroid hormones, boar taint compounds, and reproductive organs in pigs according to the delay between immunocastration and slaughter. Theriogenology. 2013;79:69–80. doi: 10.1016/j.theriogenology.2012.09.010. PubMed DOI

Ülker H., Kanter M., Gökdal Ö., Aygün T., Karakus F., Sakarya M., De Avila D., Reeves J. Testicular development, ultrasonographic and histological appearance of the testis in ram lambs immunized against recombinant LHRH fusion proteins. Anim. Reprod. Sci. 2005;86:205–219. doi: 10.1016/j.anireprosci.2004.07.011. PubMed DOI

Ülker H., Küçük M., Yilmaz A., Yörük M., Arslan L., deAvila D., Reeves J. LHRH fusion protein immunization alters testicular development, ultrasonographic and histological appearance of ram testis. Reprod. Domest. Anim. 2009;44:593–599. doi: 10.1111/j.1439-0531.2007.01024.x. PubMed DOI

Needham T., Lambrechts H., Hoffman L. Extending the interval between second vaccination and slaughter: II. Changes in the reproductive capacity of immunocastrated ram lambs. Animal. 2019;13:1962–1971. doi: 10.1017/S1751731118003609. PubMed DOI

Huxsoll C.C., Price E.O., Adams T.E. Testis function, carcass traits, and aggressive behavior of beef bulls actively immunized against gonadotropin-releasing hormone. J. Anim. Sci. 1998;76:1760–1766. doi: 10.2527/1998.7671760x. PubMed DOI

Janett F., Gerig T., Tschuor A.C., Amatayakul-Chantler S., Walker J., Howard R., Bollwein H., Thun R. Vaccination against gonadotropin-releasing factor (GnRF) with Bopriva significantly decreases testicular development, serum testosterone levels and physical activity in pubertal bulls. Theriogenology. 2012;78:182–188. doi: 10.1016/j.theriogenology.2012.01.035. PubMed DOI

Weiler U., Götz M., Schmidt A., Otto M., Müller S. Influence of sex and immunocastration on feed intake behavior, skatole and indole concentrations in adipose tissue of pigs. Animal. 2013;7:300–308. doi: 10.1017/S175173111200167X. PubMed DOI

Doran E., Whittington F.W., Wood J.D., McGivan J.D. Cytochrome P450IIE1 (CYP2E1) is induced by skatole and this induction is blocked by androstenone in isolated pig hepatocytes. Chem. Biol. Interact. 2002;140:81–92. doi: 10.1016/S0009-2797(02)00015-7. PubMed DOI

Jensen M.T., Cox R.P., Jensen B.B. 3-Methylindole (skatole) and indole production by mixed populations of pig fecal bacteria. Appl. Environ. Microb. 1995;61:3180–3184. doi: 10.1128/AEM.61.8.3180-3184.1995. PubMed DOI PMC

Wesoly R., Weiler U. Nutritional Influences on Skatole Formation and Skatole Metabolism in the Pig. Animals. 2012;2:221–242. doi: 10.3390/ani2020221. PubMed DOI PMC

Heyrman E., Kowalski E., Millet S., Tuyttens F.A.M., Ampe B., Janssens S., Buys N., Wauters J., Vanhaecke L., Aluwé M. Monitoring of behavior, sex hormones and boar taint compounds during the vaccination program for immunocastration in three sire lines. Res. Vet. Sci. 2019;124:293–302. doi: 10.1016/j.rvsc.2019.04.010. PubMed DOI

Pieterse E. Ph.D. Thesis. University of Stellenbosch; Western Cape, South Africa: Apr, 2006. Effects of Increased Slaughter Weight of Pigs on Pork Production.

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...