Simon Dellicour1,2, Philippe Lemey1, Jean Artois2, Tommy T Lam3, Alice Fusaro4, Isabella Monne4, Giovanni Cattoli4,5, Dmitry Kuznetsov6, Ioannis Xenarios7, Gwenaelle Dauphin8, Wantanee Kalpravidh9, Sophie Von Dobschuetz10, Filip Claes9, Scott H Newman11, Marc A Suchard12,13,14, Guy Baele1, Marius Gilbert2. 1. Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, 3000 Leuven, Belgium. 2. Spatial Epidemiology Lab (SpELL), Université Libre de Bruxelles, 1050 Bruxelles, Belgium. 3. State Key Laboratory of Emerging Infectious Diseases, School of Public Health, The University of Hong Kong, Hong Kong SAR, China. 4. Department of Comparative Biomedical Sciences, Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Legnaro, Italy. 5. Animal Production and Health Laboratory, Joint FAO/IAEA Division, 2444 Seibersdorf, Austria. 6. Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland. 7. Center for Integrative Genomics, University of Lausanne, 1005 Lausanne, Switzerland. 8. Ceva Santé Animale, 33500 Libourne, France. 9. Food and Agriculture Organization of the United Nations, Regional Office for Asia and the Pacific, Emergency Center of the Transboundary Animal Diseases, Bangkok 10200, Thailand. 10. Food and Agriculture Organization of the United Nations, Headquarters, Rome, Italy. 11. Food and Agriculture Organization of the United Nations, Regional Office for Africa, Accra, Ghana. 12. Department of Biomathematics, David Geffen School of Medicine, Los Angeles, CA, USA. 13. Department of Biostatistics, Fielding School of Public Health, Los Angeles, CA, USA. 14. Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Abstract
MOTIVATION: The potentially low precision associated with the geographic origin of sampled sequences represents an important limitation for spatially explicit (i.e. continuous) phylogeographic inference of fast-evolving pathogens such as RNA viruses. A substantial proportion of publicly available sequences is geo-referenced at broad spatial scale such as the administrative unit of origin, rather than more precise locations (e.g. geographic coordinates). Most frequently, such sequences are either discarded prior to continuous phylogeographic inference or arbitrarily assigned to the geographic coordinates of the centroid of their administrative area of origin for lack of a better alternative. RESULTS: We here implement and describe a new approach that allows to incorporate heterogeneous prior sampling probabilities over a geographic area. External data, such as outbreak locations, are used to specify these prior sampling probabilities over a collection of sub-polygons. We apply this new method to the analysis of highly pathogenic avian influenza H5N1 clade data in the Mekong region. Our method allows to properly include, in continuous phylogeographic analyses, H5N1 sequences that are only associated with large administrative areas of origin and assign them with more accurate locations. Finally, we use continuous phylogeographic reconstructions to analyse the dispersal dynamics of different H5N1 clades and investigate the impact of environmental factors on lineage dispersal velocities. AVAILABILITY AND IMPLEMENTATION: Our new method allowing heterogeneous sampling priors for continuous phylogeographic inference is implemented in the open-source multi-platform software package BEAST 1.10. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
MOTIVATION: The potentially low precision associated with the geographic origin of sampled sequences represents an important limitation for spatially explicit (i.e. continuous) phylogeographic inference of fast-evolving pathogens such as RNA viruses. A substantial proportion of publicly available sequences is geo-referenced at broad spatial scale such as the administrative unit of origin, rather than more precise locations (e.g. geographic coordinates). Most frequently, such sequences are either discarded prior to continuous phylogeographic inference or arbitrarily assigned to the geographic coordinates of the centroid of their administrative area of origin for lack of a better alternative. RESULTS: We here implement and describe a new approach that allows to incorporate heterogeneous prior sampling probabilities over a geographic area. External data, such as outbreak locations, are used to specify these prior sampling probabilities over a collection of sub-polygons. We apply this new method to the analysis of highly pathogenic avian influenza H5N1 clade data in the Mekong region. Our method allows to properly include, in continuous phylogeographic analyses, H5N1 sequences that are only associated with large administrative areas of origin and assign them with more accurate locations. Finally, we use continuous phylogeographic reconstructions to analyse the dispersal dynamics of different H5N1 clades and investigate the impact of environmental factors on lineage dispersal velocities. AVAILABILITY AND IMPLEMENTATION: Our new method allowing heterogeneous sampling priors for continuous phylogeographic inference is implemented in the open-source multi-platform software package BEAST 1.10. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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