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Assessing introgression of Sahelian zebu genes into native Bos taurus breeds in Burkina Faso

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Abstract

A total of 350 samples were analyzed to estimate zebu gene proportions into two different taurine cattle breeds of Burkina Faso (Lobi and N’Dama) using 38 microsatellites and various statistical methodologies. West African and East African zebu samples were sequentially used as reference parental populations. Furthermore, N’Dama cattle from Congo, the composite South African Bonsmara cattle breed and a pool of European cattle were used successively as second parental populations. Independently of the methodology applied: (a) the use of West African zebu samples gave higher admixture coefficients than the East African zebu; (b) the higher zebu proportions were estimated when the European cattle was used as parental population 2; and (c) the use of the N’Dama population from Congo as parental population 2 gave the more consistent zebu proportion estimates for both the Lobi and the N’Dama breeds. In any case, the zebu admixture proportions estimated were not negligible and were always higher in the N’Dama cattle than in the Lobi cattle of Burkina Faso. This suggested that the introgression of Sahelian zebu genes into the taurine cattle of Southern West Africa can follow a complex pattern that can depend on local agro-ecological features. The current research pointed out that the estimation of admixture coefficients is highly dependent on both the assumptions underlying the methodologies applied and the selection of parental populations. Our analyses suggest that either too high or nil genetic identity between the parental and the expectedly derived populations must be avoided.

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References

  1. Toure SM (1997) Trypanotolerance. Review of knowledge. Rev Elev Med Vet Pay 30:157–174

    Google Scholar 

  2. Hanotte O, Ronin Y, Agaba M, Nilsson P, Gelhaus A, Horstmann R, Sugimoto Y, Kemp S, Gibson J (2003) Mapping of quantitative trait loci controlling trypanotolerance in a cross of tolerant West African N’Dama and susceptible East African Boran cattle. PNAS 100:7443–7448

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  3. Freeman AR, Meghen CM, Machugh DE, Loftus RT, Achukwi MD, Bado A, Sauveroche B, Bradley DG (2004) Admixture and diversity in West African cattle populations. Mol Ecol 13:3477–3487

    Article  CAS  PubMed  Google Scholar 

  4. Agyemang K (2005) Trypanotolerant livestock in the context of trypanosomiasis intervention strategies. PAAT technical and scientific series 7. Food and Agriculture Organisation of the United Nations, Rome, Italy

  5. Soudré A, Ouédraogo-Koné S, Wurzinger M, Müller S, Hanotte O, Ouédraogo AG, Sölkner J (2013) Trypanosomosis: a priority disease in tsetse-challenged areas of Burkina Faso. Trop Anim Health Prod 45:497–503

    Article  PubMed  Google Scholar 

  6. MacHugh DE, Shriver MD, Loftus RT, Cunningham P, Bradley DG (1997) Microsatellite DNA variation and the evolution, domestication and phylogeography of taurine and zebu cattle (Bos taurus and Bos indicus). Genetics 146:1071–1086

    PubMed Central  CAS  PubMed  Google Scholar 

  7. Dayo GK, Thevenon S, Berthier D, Moazami-Goudrazi K, Denis C, Cuny G, Eggen A, Gautier M (2009) Detection of selection signatures within candidate regions underlying trypanotolerance in outbred cattle populations. Mol Ecol 18:1801–1813

    Article  CAS  PubMed  Google Scholar 

  8. Dayo GK, Gautier M, Berthier D, Poivey JP, Sidibe I, Bengaly Z, Eggen A, Boichard D, Thevenon S (2011) Association studies in QTL regions linked to bovine trypanotolerance in a West African crossbred population. Anim Genet 43:123–132

    Article  PubMed  Google Scholar 

  9. Álvarez I, Traoré A, Tambourá HH, Kaboré A, Royo LJ, Fernández I, Ouédraogo-Sanou G, Sawadogo L, Goyache F (2009) Microsatellite analysis characterizes Burkina Faso as a genetic contact zone between Sahelian and Djallonké sheep. Anim Biotechnol 20:47–57

    Article  PubMed  Google Scholar 

  10. Traoré A, Álvarez I, Tambourá HH, Fernández I, Kaboré A, Royo LJ, Gutiérrez JP, Ouédraogo-Sanou G, Sawadogo L, Goyache F (2009) Genetic characterisation of Burkina Faso goats using microsatellite polymorphism. Livest Sci 123:322–328

    Article  Google Scholar 

  11. Achukwi MD, Tanya VN, Hill EW, Bradley DG, Meghen C, Sauveroche B, Banser JT, Ndoki JN (1997) Susceptibility of the Namchi and Kapsiki cattle of Cameroon to trypanosome infection. Trop Anim Health Prod 4:219–226

    Article  Google Scholar 

  12. Orenge CO, Munga L, Kimwele VN, Kemp S, Korol A, Gibson JP, Hanotte O, Soller M (2012) Trypanotolerance in N’Dama x Boran crosses under natural trypanosome challenge: effect of test-year environment, gender, and breed composition. BMC Genetics 13:87 http://www.biomedcentral.com/1471-2156/13/87

    Google Scholar 

  13. Ruane J (1999) A critical review of the value of genetic distance studies in conservation of animal genetic resources. J Anim Breed Genet 116:317–323

    Article  Google Scholar 

  14. Jordana J, Alexandrino P, Beja-Pereira A, Bessa I, Cañon J, Carretero Y, Dunner S, Laloë D, Moazami-Gourdarzi K, Sanchez A, Ferrand N (2003) Genetic structure of eighteen local south European beef cattle breeds by comparative F-statistics analysis. J Anim Breed Genet 120(2):73–87

    Article  Google Scholar 

  15. Mahgoub O, Babiker HA, Kadim IT, Al-Kindi M, Hassan S, Al-Marzooqi W, Eltahir YE, Al-Abri MA, Al-Khayat A, Al-Sinani KR, Al-Khanjari H, Costa V, Chen S, Beja-Pereira A (2012) Disclosing the origin and diversity of Omani cattle. Anim Genet doi: 10.1111/j.1365-2052.2012.02399.x

  16. Ibeagha-Awemu E, Erhardt G (2005) Genetic structure and differentiation of 12 African Bos indicus and Bos taurus cattle breeds, inferred from protein and microsatellite polymorphisms. J Anim Breed Genet 122:12–20

    Article  CAS  PubMed  Google Scholar 

  17. Ndumu DB, Baumung R, Hanotte O, Wurzinger M, Okeyo MA, Jianlin H, Kibogo H, Sölkner J (2008) Genetic and morphological characterisation of the Ankole Longhorn cattle in the African Great Lakes region. Genet Sel Evol 40:467–490

    PubMed Central  PubMed  Google Scholar 

  18. Missohou A, Poutya MR, Nenonene A, Dayo G-K, Ayssiwede SB, Talaki E, Issa Y, Fané A (2011) Genetic diversity and differentiation in nine West African local goat breeds assessed via microsatellite polymorphism. Small Rum Res 99:20–24

    Article  Google Scholar 

  19. Zerabruk M, Li M-H, Kantanen J, Olsaker I, Ibeagha-Awemu EM, Erhardt G, Vangen O (2012) Genetic diversity and admixture of indigenous cattle from North Ethiopia: implications of historical introgressions in the gateway region to Africa. Anim Genet 43:257–266

    Article  CAS  PubMed  Google Scholar 

  20. Dadi H, Tibbo M, Takahashi Y, Nomura K, Hanada H, Amano T (2008) Microsatellite analysis reveals high genetic diversity but low genetic structure in Ethiopian indigenous cattle populations. Anim Genet 39:425–431

    Article  CAS  PubMed  Google Scholar 

  21. Hanotte O, Bradley DG, Ochieng JW, Verjee Y, Hill EW, Rege JE (2002) African pastoralism: genetic imprints of origins and migrations. Science 296:336–339

    Article  CAS  PubMed  Google Scholar 

  22. Traoré A, Álvarez I, Fernández I, Pérez-Pardal L, Kaboré A, Ouédraogo-Sanou GMS, Zaré Y, Tamboura HH, Goyache F (2012) Ascertaining gene flow patterns in livestock populations of developing countries: a case study in Burkina Faso goat. BMC Genet 13:35. doi:10.1186/1471-2156-13-35

    Article  PubMed Central  PubMed  Google Scholar 

  23. Bouyer J, Balenghien T, Ravel S, Vial L, Sidibé I, Thévenon S, Solano P, De Meeûs T (2009) Population sizes and dispersal patterns of tsetse flies: rolling on the river? Mol Ecol 18:2787–2797

    Article  CAS  PubMed  Google Scholar 

  24. Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor

    Google Scholar 

  25. Bozzi R, Álvarez I, Crovetti A, Fernández I, De Petris D, Goyache F (2012) Assessing priorities for conservation in Tuscan cattle breeds using microsatellites. Animal 6:203–211

    Article  CAS  PubMed  Google Scholar 

  26. Gutiérrez JP, Royo LJ, Álvarez I, Goyache F (2005) MolKin v2.0: a computer program for genetic analysis of populations using molecular coancestry information. J Hered 96:718–721

    Article  PubMed  Google Scholar 

  27. Caballero A, Toro MA (2002) Analysis of genetic diversity for the management of conserved subdivided populations. Conserv Genet 3:289–299

    Article  CAS  Google Scholar 

  28. Álvarez I, Gutiérrez JP, Royo LJ, Fernández I, Gómez E, Arranz JJ, Goyache F (2005) Testing the usefulness of the molecular coancestry information to assess genetic relationships on livestock using a set of Spanish sheep breeds. J Anim Sci 83:737–744

    PubMed  Google Scholar 

  29. Eding H, Meuwissen THE (2001) Marker-based estimates of between and within population kinships for the conservation of genetic diversity. J Anim Breed Genet 118:141–159

    Article  CAS  Google Scholar 

  30. Eding H, Crooijmans RPMA, Groenen MAM, Meuwissen THE (2002) Assessing the contribution of breeds to genetic diversity in conservation schemes. Genet Sel Evol 34:613–633

    Article  PubMed Central  PubMed  Google Scholar 

  31. Simianer H (2002) Molekulargenetische Differenzierung verschiedener Rotviehpopulationen. Schriftenreihe des Bundesministeriums für Verbraucherschutz, Ernährung und Landwirtschaft. Heft 493. Landwirtschaftsverlag GmbH. Münster-Hiltrup, Germany

  32. Baumung R, Cubric-Curik V, Schwend K, Achmann R, Sölkner J (2006) Genetic characterisation and breed assignment in Austrian sheep breeds using microsatellite marker information. J Anim Breed Genet 123:265–271

    Article  CAS  PubMed  Google Scholar 

  33. Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959

    PubMed Central  CAS  PubMed  Google Scholar 

  34. Beaumont M, Barret EM, Gotelli D, Kitchener AC, Daniels J, Pritchard J (2001) Genetic diversity and introgression in the Scottish wildcat. Mol Ecol 10:319–336

    Article  CAS  PubMed  Google Scholar 

  35. Kumar P, Freeman AR, Loftus RT, Gaillard C, Fuller DQ, Bradley DG (2003) Admixture analysis of South Asian cattle. Heredity 91:43–50

    Article  CAS  PubMed  Google Scholar 

  36. Wang J (2003) Maximum-likelihood estimation of admixture proportions from genetic data. Genetics 164:747–765

    PubMed Central  PubMed  Google Scholar 

  37. Chikhi L, Bruford MW, Beaumont MA (2001) Estimation of admixture proportions: a likelihood-based approach using Markov chain Monte Carlo. Genetics 158:1347–1362

    PubMed Central  CAS  PubMed  Google Scholar 

  38. Bray TC, Chikhi L, Sheppy AJ, Bruford MW (2009) The population genetic effects of ancestry and admixture in a subdivided cattle breed. Anim Genet 40:393–400

    Article  CAS  PubMed  Google Scholar 

  39. Ibeagha-Awemu E, Jann O, Weimann C, Erhardt G (2004) Genetic diversity, introgression and relationships among West/Central African cattle breeds. Genet Sel Evol 36:673–690

    Article  PubMed Central  PubMed  Google Scholar 

  40. Itard J, Cuisance D (2003) Vecteurs cycliques des trypanosomoses. In: Lefèvre PC, editor. Principales Maladies Infectieuses et Parasitaires du Bétail. Europe et Régions Chaudes. Lavoisier, pp 139–165

  41. Pérez-Pardal L, Royo LJ, Beja-Pereira A, Chen S, Cantet RJC, Traoré A, Curik I, Sölkner J, Bozzi R, Fernández I, Álvarez I, Gutiérrez JP, Gómez E, Ponce de León FA, Goyache F (2010) Multiple paternal origins of domestic cattle revealed by Y-specific interspersed multilocus microsatellites. Heredity 105:511–519

    Article  PubMed  Google Scholar 

  42. Bertorelle G, Excoffier L (1998) Inferring admixture proportions from molecular data. Mol Biol Evol 15:1298–1311

    Article  CAS  PubMed  Google Scholar 

  43. Dupanloup I, Bertorelle G (2001) Inferring admixture proportions from molecular data: extension to any number of parental populations. Mol Biol Evol 18:672–675

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This paper was partially funded by grants from CORAF/WECARD-World Bank no. 03/GRN/16 and from MICIN-FEDER No. AGL2011-27585. No ethics statement was required for the collection of DNA samples. DNA was extracted from blood samples obtained from different veterinary practitioners visiting farms with the permission of the owners.

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Correspondence to F. Goyache.

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Álvarez, I., Traoré, A., Fernández, I. et al. Assessing introgression of Sahelian zebu genes into native Bos taurus breeds in Burkina Faso. Mol Biol Rep 41, 3745–3754 (2014). https://doi.org/10.1007/s11033-014-3239-x

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  • DOI: https://doi.org/10.1007/s11033-014-3239-x

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