Abstract
Bovine tuberculosis (bTB), widely considered a disease of livestock, can also affect large game species despite their poorly understood role in the epidemiology of the endemic state of the disease. The Idanha-a-Nova County, situated in the eastern region of central Portugal, is one of the most important regions for large game hunting activity. In order to investigate the role of large game and the presence of bTB in Idanha-a-Nova, 132 wild boar (Sus scrofa) and 339 red deer (Cervus elaphus) were inspected for bTB-compatible lesions (bTBCL) during the 2008–2009 hunting season. Tissue samples with bTBCL were collected and processed for bacteriological confirmation and spoligotyping of Mycobacterium bovis isolates. In wild boar, bTB lesions were single, mostly calcified (21/29, 72.4%) and situated in the mandibular lymph nodes. Lesions were more severe and largely non-calcified (36/40, 90%) in red deer. Wild boar presented a consistently higher bTB infection rate than the red deer; however, the difference was only significant in the southern B area. This area was significantly affected by bTB for both animal species (up to 72.7% in wild boar and 34.8% in red deer) and requires the urgent implementation of intervention measures to contain the disease. Wild boar may assume an important role in the emergence of new disease foci in distant areas that infected red deer cannot reach. Spoligotyping of M. bovis isolates grouped the strains into three clusters, revealing patterns common to wild boar, red deer, and also to local cattle, indicating possible transmission among different animal species.
Similar content being viewed by others
References
Anonymous (2009) Lazer/Caça e Pesca. http://www.cm-idanhanova.pt/lazer/caca_pesca.html [accessed 25 November 2009]
Anonymous (2010) Tuberculose bovina: relatório técnico. Direcção Geral de Veterinária, DGV, Portugal.
Aranaz A, Juan L, Montero N, Sánchez C, Galka M, Delso C, Álvarez J, Romero B, Bezos J, Vela A, Briones V, Mateos A, Dominguez L (2004) Bovine tuberculosis (Mycobacteria bovis) in wildlife in Spain. J Clin Microbiol 42(6):2602–2608
Bollo E, Ferroglio E, Dini V, Mignone W, Biolatti B, Rossi L (2000) Detection of Mycobacterium tuberculosis complex in lymph nodes of wild boar (Sus scrofa) by a target-amplified test system. J Vet Med B 47:337–342
Corner LAL (2006) The role of wild animal populations in the epidemiology of tuberculosis in domestic animals: How to assess the risk. Vet Microbiol 112:303–312
Daniel WW (1987) Biostatistics: A Foundation for Analysis in the Health Sciences. Wiley, Canada, p 734
Duarte EL, Domingos M, Amado A, Botelho A (2008) Spoligotype diversity of Mycobacterium bovis and Mycobacterium caprae animal isolates. Vet Microbiol 130(3–4):415–421
ESRI (2010) http://www.esri.com/software/arcgis/extensions/networkanalyst
European Regulation (EC) Nº 853/2004 of the European Parliament and of the Council of 29 April 2004. (2004) Laying down specific hygiene rules for food of animal origin. Official Journal of the European Union L 139/55
Goodchild MF, Haining RP (2004) GIS and spatial data analysis: covering perspectives. Pap Reg Sci 83:363–385
Goovaerts P (1997) Geoestatistics for Natural Resources Evaluation. Oxford University Press, New York
Gortázar C, Ferroglio E, Höfle U, Frölich K, Vicente J (2007) Diseases shared between wildlife and livestock: a European perspective. Eur J Wildl Res 53:241–256
Hengl T (2007) A Practical guide to Geoestatistical Mapping of Environmental Variables. European Commission, Joint Research Center–Institute for Environment and Sustainability, Office for Official Publications oh the European Communities, Luxembourg
Hoef JM, Johnston K, Lucas N, Krivoruchko K (2001) Using ArcGIS Geostatistical Analyst. ESRI, USA
Kamerbeek J, Schouls L, Kolk A, Van Agterveld M, Van Soolingen D, Kuijper S, Bunschoten A, Molhuizen H, Shaw R, Goyal M, Van Embden J (1997) Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol 35:907–914
Kremer K, Van Soolingen D, Frothingham R, Haas WH, Hermans PWM, Martin C, Palittapongarnpim P, Plikaytis BB, Riley LW, Yakrus MA, Musser JM, Van Embden JDA (1999) Comparison of methods based on different molecular epidemiological markers for typing Mycobacterium tuberculosis complex strains: interlaboratory study power and reproducibility. J Clin Microbiol 37:2607–2618
Martín-Hernando MP, Hofle U, Vicente J, Ruiz-Fons F, Vidal D, Barral M, Garrido JM, de la Fuente J, Gortázar C (2007) Lesions associated with Mycobacterium tuberculosis complex infection in the European wild boar. Tuberculosis 87:360–367
Matos F, Cunha MV, Canto A, Albuquerque T, Amado A, Botelho A (2010) Snapshot of Mycobacterium bovis and Mycobacterium caprae infections in livestock in an area with a low incidence of bovine tuberculosis. J Clin Microbiol 48:4337–4339
Mendoza JH, Parra A, Tato A, Alonso JM, Rey JM, Peña J, Garcia Sánchez A, Larrasa J, Teixidó J, Manzano G, Cerrato R, Pereira G, Fernandez-Llario P, Hermoso de Mendoza M (2006) Bovine tuberculosis in wild boar (Sus scrofa), red deer (Cervus elaphus) and cattle (Bos taurus) in a Mediterranean ecosystem (1992–2004). Prev Vet Med 74:239–247
Niemann S, Harmsen D, Rusch-Gerdes S, Richter E (2000) Differentiation of clinical Mycobacterium tuberculosis complex isolates by gyr B DNA sequence polymorphism analysis. J Clin Microbiol 38:3231–3234
OIE (2004) Manual of diagnostic tests and vaccines for terrestrial animals, 5th edn. Word Organisation for Animal Health-OIE, Paris
Parra A, Larrasa J, Garcia A, Alonso JM, Hermoso de Mendoza J (2005) Molecular epidemiology of bovine tuberculosis in wild animals in Spain: a first approach to risk factor analysis. Vet Microbiol 110(3–4):293–300
Phillips CJ, Foster CR, Morris PA, Teverson R (2003) The transmission of Mycobacterium bovis infection to cattle. Res Vet Sci 74:1–15
Santos N, Correia-Neves M, Ghebremichael S, Kallenius G, Svenson SB, Almeida V (2009) Epidemiology of Mycobacterium bovis infection in wild boar (Sus scrofa) from Portugal. J Wildl Dis 45(4):1048–1061
Schröder W (2006) GIS, geostatistics, metada banking, and tree-based models for data analysis and mapping in environmental monitoring and epidemiology. Int J Med Microbiol 296(1):23–36
Serraino A, Marche IG, Sanguine V, Rossi MC, Zanoni RG, Catozzi L, Bandera A, Dini W, Mignone W, Franze IF, Gori A (1999) Monitoring of transmission of tuberculosis between wild boar and cattle: genotypical analysis, of strains by molecular epidemiology techniques. J Clin Microbiol 37:2766–2771
Snedecor GW, Cochran WG (1995) Statistical Methods, 8th edn. Iowa State University Press, AMES, p 503
Van Embden JDA, Van Gorkom T, Kremer K, Jansen R, Vander Zeijst BAM, Schouls LM (2000) Genetic variation and evolutionary origin of the Direct Repeat locus of Mycobacterium tuberculosis complex bacteria. J Bacteriol 182:2393–2401
Vicente J, Höfle U, Garrido JM, Fernández-De-Mera IG, Acevedo P, Juste R, Barral M, Gortázar C (2006) Wild boar and red deer display high prevalences of tuberculosis-like lesions in Spain. Vet Res 37:107–119
Zanella G, Duvauchelle JH, Moutou ML, Durand B (2008) Patterns of lesions of bovine tuberculosis in wild red deer and wild boar. Vet Rec 163(2):43–47
Acknowledgments
The authors would like to thank to Dr. António Manteigas, from Veterinary Services of Castelo-Branco–DIVCB, for all the help provided during the development of this study. Thanks are also due to the anonymous referee for valuable comments to the improvement of the manuscript.
Author information
Authors and Affiliations
Corresponding author
Additional information
Communicated by C. Gortázar
Rights and permissions
About this article
Cite this article
Vieira-Pinto, M., Alberto, J., Aranha, J. et al. Combined evaluation of bovine tuberculosis in wild boar (Sus scrofa) and red deer (Cervus elaphus) from Central-East Portugal. Eur J Wildl Res 57, 1189–1201 (2011). https://doi.org/10.1007/s10344-011-0532-z
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10344-011-0532-z