Skip to main content

Population structure and genetic variability in the Murrah dairy breed of water buffalo in Brazil accessed via pedigree analysis

Abstract

The objective of this study was to use pedigree analysis to evaluate the population structure and genetic variability in the Murrah dairy breed of water buffalo (Bubalus bubalis) in Brazil. Pedigree analysis was performed on 5,061 animals born between 1972 and 2002. The effective number of founders (fe) was 60, representing 6.32 % of the potential number of founders. The effective number of ancestors (fa) was 36 and the genetic contribution of the 17 most influent ancestors explained 50 % of the genetic variability in the population. The ratio fe/fa (effective number of founders/effective number of ancestors), which expresses the effect of population bottlenecks, was 1.66. Completeness level for the whole pedigree was 76.8, 49.2, 27.7, and 12.8 % for, respectively, the first, second, third, and fourth known parental generations. The average inbreeding values for the whole analyzed pedigree and for inbreed animals were, respectively, 1.28 and 7.64 %. The average relatedness coefficient between individuals of the population was estimated to be 2.05 %—the highest individual coefficient was 10.31 %. The actual inbreeding and average relatedness coefficient are probably higher than estimated due to low levels of pedigree completeness. Moreover, the inbreeding coefficient increased with the addition of each generation to the pedigree, indicating that incomplete pedigrees tend to underestimate the level of inbreeding. Introduction of new sires with the lowest possible average relatedness coefficient and the use of appropriate mating strategies are recommended to keep inbreeding at acceptable levels and increase the genetic variability in this economically important species, which has relatively low numbers compared to other commercial cattle breeds. The inclusion of additional parameters, such as effective number of founders, effective number of ancestors, and fe/fa ratio, provides better resolution as compared to the inclusion of inbreeding coefficient and may help breeders and farmers adopt better precautionary measures against inbreeding depression and other deleterious genetic effects.

This is a preview of subscription content, access via your institution.

Fig. 1
Fig. 2
Fig. 3

References

  • Alderson, G.H.L. 1991. A system to maximize the maintenance of genetic variability in small populations. In Conservation of Domestic Livestock (ed. L. Alderson & L. Bodo), 18-19. Wallingford, UK: CAB International.

    Google Scholar 

  • Boichard, D., Maignel, L. and Verriel, E., 1997. The value of using probabilities of gene origin to measure genetic variability in a population. Genetics Selection Evolution, 29, 5--23.

    Article  Google Scholar 

  • Carneiro, P.L.S., Malhado, C.H.M., Martins Filho, R., Carneiro, A.P.S., Silva F.F. and Torres R.A., 2009. The Indubrasil breed in the Brazilian Northeast: breeding and population structure. Revista Brasileira de Zootecnia, 38, 2327--2334.

    Article  Google Scholar 

  • Dunner S., Checa M.L., Gutiérrez J.P., Martín J.P., Cañón J. 1998. Genetic analysis and management in small populations: the Asturcon pony as an example. Genetic Selection Evolution, 30, 397–405.

    Article  Google Scholar 

  • Faria, F.J.C., Vercesi Filho, A.E., Madalena, F.E. and Josahkian, L.A., 2002. Population structure of the polled Nelore breed. Arquivo Brasileiro Medicina Veterinária Zootecnia, 54, 501--509.

    Article  Google Scholar 

  • Faria, F.J.C., Vercesi Filho, A.E., Madalena, F.E. and Josahkian, L.A, 2004. Population structure of the Sindi breed from Brazil. Revista Brasileira de Zootecnia, 33, 852--857.

    Article  Google Scholar 

  • FAO, 2000. Water buffalo: an asset undervalued. FAO Regional Office for Asia and the Pacific, Bangkok, Thailand.

    Google Scholar 

  • Frankham, R. 1995. Conservation genetics. Annual Review of Genetics. 29, 305-327.

    PubMed  Article  CAS  Google Scholar 

  • Głażewska, I. and Jezierski, T., 2004. Pedigree analysis of Polish Arabian Horses based on founder contributions. Livestock Production Science, 90, 293--298.

    Article  Google Scholar 

  • Goyache, F., Gutierrez, J.P., Fernandez, I., Gomes, E., Alvarez, I., Díez, J. and Royo, L.J., 2003. Using pedigree information to monitor genetic variability of endangered population: the Xalda sheep breed of Asturias as an example. Journal of Animal Breeding and Genetics, 120, 95--105.

    Article  Google Scholar 

  • Goyache, F., Fernández, I., Espinosa, M.A., Payeras, L., Pérez-Pardal, L., Gutiérrez, J.P., Royo, L.J. and Álvarez, I, 2010. Análisis demográfico y genético de la raza ovina Mallorquin. ITEA, 106, 3--14.

    Google Scholar 

  • Gutiérrez, J.P., Altarriba, J., Díaz, C., Quintanilla, R. Cañón, J. and Piedrafita, J. 2003. Pedigree analysis of eight Spanish beef cattle breeds. Genetic Selection Evolution, 35, 43–64.

    Article  Google Scholar 

  • Gutiérrez J.P. and Goyache, F., 2005. A note on ENDOG: a computer program for analysing pedigree information. Journal Animal Breeding and Genetics, 122, 172--176.

    Article  Google Scholar 

  • Jain, A.K., Kumar, R., Mehra, M.L. and Trehan, P.K., 2007. Incidence of inbreeding and its effect on production traits in a graded Murrah herd. Indian Journal of Animal Sciences, 77, 1155--1157.

    Google Scholar 

  • Kumar, R. and Singh, R., 2010. Buffalo production system in India. Revista Veterinaria, 21, 32—37.

    Google Scholar 

  • Lacy, R.C. 1989. Analysis of founder representation in pedigrees: founder equivalents and founder genome equivalents. Zoo Biology, 8, 111-123.

    Article  Google Scholar 

  • Maccluer, J.W., Boyce, A.J., Dyke, B., Weitkamp, L.R., Fenning, D.W. and Parsons, C.J., 1983. Inbreeding and pedigree structure in Standard bred horses. Journal of Heredity, 74, 394--399.

    Google Scholar 

  • Maignel, L., Boichard, D. and Verrier, E., 1996. Genetic variability of French dairy breeds estimated from pedigree information. Interbull Bull, 14, 49—54.

    Google Scholar 

  • Malécot, G., 1969. The mathematics of heredity, translated by DM Yermanos. Freeman, San Francisco

    Google Scholar 

  • Malhado, C.H.M., Ramos, A.A., Carneiro, P.L.S., Souza, J.C. and Piccinin, A., 2007. Genetic and phenotypic parameters for milk production of Murrah buffaloes. Revista Brasileira de Zootecnia, 36, 376--379.

    Article  Google Scholar 

  • Malhado, C.H.M, Ramos, A.A., Carneiro, P.L.S., Azevedo, D.M.M.R., Souza, J.C., Martins and Filho. R., 2008. Improvement and population structure of Mediterranean water buffaloes raised in Brazil. Pesquisa Agropecuária Brasileira, 43, 215--220.

    Google Scholar 

  • Malhado, C.H.M., Carneiro, P.L.S., Malhado, A.C.M., Martins Filho, R., Bozzi, R. and Ladle, R.J., 2010. Genetic improvement and population structure of the Nelore breed in Northern Brazil. Pesquisa Agropecuária Brasileira, 45, 1109--1116.

    Article  Google Scholar 

  • Marcondes, C.R, Vozzi, P.A, Cunha, B.R.N, Lôbo, R.B, Araújo, C.V. and Marques, J.R.F., 2010. Genetic variability in water buffalo from nucleous herd by pedigree analysis. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 62, 706--711.

    Article  Google Scholar 

  • Martínez, R.A., García, D., Gallego, J.L., Onofre, G., Pérez, J. and Cañón, J., 2008. Genetic variability in Colombian Creole cattle populations estimated by pedigree information. Journal of Animal Science, 86, 545--552.

    PubMed  Article  Google Scholar 

  • Mcparland, S., Kearney, J.F., Rath, M. and Berry, D.P., 2007. Inbreeding effects on milk production, calving performance, fertility, and conformation in Irish Holstein-Friesians. Journal of Dairy Science, 90, 4411--4419.

    Article  CAS  Google Scholar 

  • Meuwissen, T.H.E. and Luo, Z., 1992. Computing inbreeding coefficients in large populations. Genetic Selection Evolution, 24, 305--313.

    Article  Google Scholar 

  • Miglior, F., Burnside, E.B. Dekkers, J.C. 1995. Nonadditive genetic effects and inbreeding depression for somatic cell counts of Holstein cattle. Journal of Dairy Science, 78, 168-1173.

    Google Scholar 

  • Ramos, A.A., Wechsler, F.S., Van Onselen, V.J., Goncalves and H.C. Promebul, 2002. Summary of buffalo Sire. Botucatu: Unesp, 39p.

  • Ramos, A.A., Malhado, C.H.M., Carneiro, P.L.S., Azêvedo, D.M.M.R. and Gonçalves, H.C., 2006. Phenotypic and genetic characterization of the milk yield and calving interval in buffalo of the Murrah breed. Pesquisa Agropecuária Brasileira, 41, 1261--1267.

    Article  Google Scholar 

  • Sheikh, P.A., Merry, F.D. and McGrath D.G., 2006. Water buffalo and cattle ranching in the Lower Amazon Basin: Comparisons and conflicts. Agricultural Systems, 87, 313–330.

    Article  Google Scholar 

  • Valera, M., Molina, A., Gutierréz, J.P., Gómez, J. and Goyache F., 2005. Pedigree analysis in the Andalusian horse: population structure, genetic variability and influence of the Carthusian strain. Livestock Production Science, 95, 57--66.

    Article  Google Scholar 

  • Vassalo, J.M., Diaz, C., Garcia-Medina, J.R., 1986. A note on the population structure of the Avileña breed of cattle in Spain. Livestock Production Science, 15, 285-288.

    Article  Google Scholar 

  • Vercesi F.A.E., Faria, F.J.C., Madalena, F.E. and Josahkian, L.A., 2002. Population structure of the registered Tabapuã cattle in Brazil. Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 54, 609--617.

    Article  Google Scholar 

  • Vijh, R.K.: Tantia, M.S., Mishra, B. and Bharani Kumar, S.T., 2008. Genetic relationship and diversity analysis of Indian water buffalo (Bubalus bubalis). Journal of Animal Science, 86, 1495--1450.

    PubMed  Article  CAS  Google Scholar 

  • Vozzi, P.A., Marcondes, C.R, Magnabosco, C.U., Bezerra, L.A.F. and Lôbo, R.B., 2006. Structure and genetic variability in Nellore (Bos indicus) cattle by pedigree analysis. Genetic Molecular Biology, 29, 482--485.

    Article  CAS  Google Scholar 

  • Vozzi, P.A., Marcondes, C.R., Bezerra, L.A. and Lôbo, R.B., 2007. Pedigree analyses in the Breeding Program for Nellore Cattle. Genetics and Molecular Research, 6, 1044--1050.

    PubMed  CAS  Google Scholar 

  • Wall, E., Brotherstone, S., Kearney, J.F., Woolliams, J.A., Coffey, M.P. 2005. Impact of nonadditive genetic effects in the estimation of breeding values for fertility and correlated traits. Journal of Dairy Science, 88, 376-385

    PubMed  Article  CAS  Google Scholar 

Download references

Acknowledgments

This research was supported by the National Counsel of Technological and Scientific Development (CNPq). The authors thank Dr. Richard Ladle for the insightful comments and proofreading the manuscript.

Author information

Affiliations

Authors

Corresponding author

Correspondence to Akin Pala.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Malhado, C.H.M., Malhado, A.C.M., Carneiro, P.L.S. et al. Population structure and genetic variability in the Murrah dairy breed of water buffalo in Brazil accessed via pedigree analysis. Trop Anim Health Prod 44, 1891–1897 (2012). https://doi.org/10.1007/s11250-012-0153-x

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11250-012-0153-x

Keywords

  • Average relatedness coefficient
  • Completeness pedigree
  • Inbreeding coefficient