Spatial and Temporal Phylogeny of Border Disease Virus in Pyrenean Chamois (Rupicapra p. pyrenaica).

Autor: Luzzago C; Department of Veterinary Medicine, University of Milan, Milano, Italy.; Centro di Ricerca Coordinata Epidemiologia e Sorveglianza Molecolare delle Infezioni-EpiSoMI, University of Milan, Milano, Italy., Ebranati E; Centro di Ricerca Coordinata Epidemiologia e Sorveglianza Molecolare delle Infezioni-EpiSoMI, University of Milan, Milano, Italy.; Department of Biomedical and Clinical Sciences 'L.Sacco', University of Milan, Milano, Italy., Cabezón O; Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain., Fernández-Sirera L; Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain., Lavín S; Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain., Rosell R; Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.; Departament d'Agricultura, Alimentació i Acció Rural, Generalitat de Catalunya, Barcelona, Spain., Veo C; Department of Biomedical and Clinical Sciences 'L.Sacco', University of Milan, Milano, Italy., Rossi L; Department of Veterinary Sciences, University of Torino, Grugliasco, Torino, Italy., Cavallero S; Department of Public Health and Infectious Diseases, Section of Parasitology, Sapienza University of Rome, Roma, Italy., Lanfranchi P; Department of Veterinary Medicine, University of Milan, Milano, Italy., Marco I; Servei d'Ecopatologia de Fauna Salvatge, Departament de Medicina i Cirurgia Animals, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain., Zehender G; Centro di Ricerca Coordinata Epidemiologia e Sorveglianza Molecolare delle Infezioni-EpiSoMI, University of Milan, Milano, Italy.; Department of Biomedical and Clinical Sciences 'L.Sacco', University of Milan, Milano, Italy.
Jazyk: angličtina
Zdroj: PloS one [PLoS One] 2016 Dec 29; Vol. 11 (12), pp. e0168232. Date of Electronic Publication: 2016 Dec 29 (Print Publication: 2016).
DOI: 10.1371/journal.pone.0168232
Abstrakt: Border disease virus (BDV) affects a wide range of ruminants worldwide, mainly domestic sheep and goat. Since 2001 several outbreaks of disease associated to BDV infection have been described in Pyrenean chamois (Rupicapra pyrenaica pyrenaica) in Spain, France and Andorra. In order to reconstruct the most probable places of origin and pathways of dispersion of BDV among Pyrenean chamois, a phylogenetic analysis of 95 BDV 5'untranslated sequences has been performed on chamois and domestic ungulates, including novel sequences and retrieved from public databases, using a Bayesian Markov Chain Monte Carlo method. Discrete and continuous space phylogeography have been applied on chamois sequences dataset, using centroid positions and latitude and longitude coordinates of the animals, respectively. The estimated mean evolutionary rate of BDV sequences was 2.9×10-3 subs/site/year (95% HPD: 1.5-4.6×10-3). All the Pyrenean chamois isolates clustered in a unique highly significant clade, that originated from BDV-4a ovine clade. The introduction from sheep (dated back to the early 90s) generated a founder effect on the chamois population and the most probable place of origin of Pyrenean chamois BDV was estimated at coordinates 42.42 N and 1.9 E. The pathways of virus dispersion showed two main routes: the first started on the early 90s of the past century with a westward direction and the second arise in Central Pyrenees. The virus spread westward for more than 125 km and southward for about 50km and the estimated epidemic diffusion rate was about 13.1 km/year (95% HPD 5.2-21.4 km/year). The strong spatial structure, with strains from a single locality segregating together in homogeneous groups, and the significant pathways of viral dispersion among the areas, allowed to reconstruct both events of infection in a single area and of migrations, occurring between neighboring areas.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE
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