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West Nile virus spread in Europe: Phylogeographic pattern analysis and key drivers.
Lu, Lu; Zhang, Feifei; Oude Munnink, Bas B; Munger, Emmanuelle; Sikkema, Reina S; Pappa, Styliani; Tsioka, Katerina; Sinigaglia, Alessandro; Dal Molin, Emanuela; Shih, Barbara B; Günther, Anne; Pohlmann, Anne; Ziegler, Ute; Beer, Martin; Taylor, Rachel A; Bartumeus, Frederic; Woolhouse, Mark; Aarestrup, Frank M; Barzon, Luisa; Papa, Anna; Lycett, Samantha; Koopmans, Marion P G.
Afiliação
  • Lu L; Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Zhang F; Usher Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Oude Munnink BB; Usher Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Munger E; Erasmus MC, Viroscience and Pandemic and Disaster Preparedness Centre, Rotterdam, the Netherlands.
  • Sikkema RS; Erasmus MC, Viroscience and Pandemic and Disaster Preparedness Centre, Rotterdam, the Netherlands.
  • Pappa S; Erasmus MC, Viroscience and Pandemic and Disaster Preparedness Centre, Rotterdam, the Netherlands.
  • Tsioka K; Department of Microbiology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Sinigaglia A; Department of Microbiology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Dal Molin E; Department of Molecular Medicine, University of Padova, Padua, Italy.
  • Shih BB; Department of Molecular Medicine, University of Padova, Padua, Italy.
  • Günther A; Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Pohlmann A; Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Riems, Germany.
  • Ziegler U; Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Riems, Germany.
  • Beer M; Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, Greifswald-Riems, Germany.
  • Taylor RA; Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Riems, Germany.
  • Bartumeus F; Department of Epidemiological Sciences, Animal and Plant Health Agency, United Kingdom.
  • Woolhouse M; Centre for Advanced Studies of Blanes (CEAB-CSIC), Girona, Spain.
  • Aarestrup FM; Centre for Research on Ecology and Forestry Applications (CREAF), Barcelona, Spain.
  • Barzon L; Catalan Institution for Research and Advanced Studies (ICREA), Barcelona, Spain.
  • Papa A; Usher Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Lycett S; Research Group for Genomic Epidemiology, Technical University of Denmark, Kongens Lyngby, Denmark.
  • Koopmans MPG; Department of Molecular Medicine, University of Padova, Padua, Italy.
PLoS Pathog ; 20(1): e1011880, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38271294
ABSTRACT

BACKGROUND:

West Nile virus (WNV) outbreaks in birds, humans, and livestock have occurred in multiple areas in Europe and have had a significant impact on animal and human health. The patterns of emergence and spread of WNV in Europe are very different from those in the US and understanding these are important for guiding preparedness activities.

METHODS:

We mapped the evolution and spread history of WNV in Europe by incorporating viral genome sequences and epidemiological data into phylodynamic models. Spatially explicit phylogeographic models were developed to explore the possible contribution of different drivers to viral dispersal direction and velocity. A "skygrid-GLM" approach was used to identify how changes in environments would predict viral genetic diversity variations over time.

FINDINGS:

Among the six lineages found in Europe, WNV-2a (a sub-lineage of WNV-2) has been predominant (accounting for 73% of all sequences obtained in Europe that have been shared in the public domain) and has spread to at least 14 countries. In the past two decades, WNV-2a has evolved into two major co-circulating clusters, both originating from Central Europe, but with distinct dynamic history and transmission patterns. WNV-2a spreads at a high dispersal velocity (88km/yr-215 km/yr) which is correlated to bird movements. Notably, amongst multiple drivers that could affect the spread of WNV, factors related to land use were found to strongly influence the spread of WNV. Specifically, the intensity of agricultural activities (defined by factors related to crops and livestock production, such as coverage of cropland, pasture, cultivated and managed vegetation, livestock density) were positively associated with both spread direction and velocity. In addition, WNV spread direction was associated with high coverage of wetlands and migratory bird flyways.

CONCLUSION:

Our results suggest that-in addition to ecological conditions favouring bird- and mosquito- presence-agricultural land use may be a significant driver of WNV emergence and spread. Our study also identified significant gaps in data and the need to strengthen virological surveillance in countries of Central Europe from where WNV outbreaks are likely seeded. Enhanced monitoring for early detection of further dispersal could be targeted to areas with high agricultural activities and habitats of migratory birds.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre do Nilo Ocidental / Vírus do Nilo Ocidental Tipo de estudo: Prognostic_studies / Screening_studies Limite: Animals / Humans País/Região como assunto: Europa Idioma: En Revista: PLoS Pathog Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Febre do Nilo Ocidental / Vírus do Nilo Ocidental Tipo de estudo: Prognostic_studies / Screening_studies Limite: Animals / Humans País/Região como assunto: Europa Idioma: En Revista: PLoS Pathog Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido