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West Nile Virus and Tick-Borne Encephalitis Virus Are Endemic in Equids in Eastern Austria
P. de Heus, J. Kolodziejek, Z. Hubálek, K. Dimmel, V. Racher, N. Nowotny, JV. Cavalleri
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2009
Free Medical Journals
od 2009
PubMed Central
od 2009
Europe PubMed Central
od 2009
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
34578454
DOI
10.3390/v13091873
Knihovny.cz E-zdroje
- MeSH
- endemické nemoci veterinární MeSH
- Equidae virologie MeSH
- Flavivirus imunologie MeSH
- infekce viry z rodu Flavivirus epidemiologie veterinární MeSH
- klíšťová encefalitida epidemiologie veterinární MeSH
- koně MeSH
- nemoci koní epidemiologie MeSH
- protilátky virové krev MeSH
- průřezové studie MeSH
- rizikové faktory MeSH
- séroepidemiologické studie MeSH
- virus západního Nilu imunologie MeSH
- viry klíšťové encefalitidy imunologie MeSH
- západonilská horečka epidemiologie veterinární MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Rakousko MeSH
The emergence of West Nile virus (WNV) and Usutu virus (USUV) in addition to the autochthonous tick-borne encephalitis virus (TBEV) in Europe causes rising concern for public and animal health. The first equine case of West Nile neuroinvasive disease in Austria was diagnosed in 2016. As a consequence, a cross-sectional seroprevalence study was conducted in 2017, including 348 equids from eastern Austria. Serum samples reactive by ELISA for either flavivirus immunoglobulin G or M were further analyzed with the plaque reduction neutralization test (PRNT-80) to identify the specific etiologic agent. Neutralizing antibody prevalences excluding vaccinated equids were found to be 5.3% for WNV, 15.5% for TBEV, 0% for USUV, and 1.2% for WNV from autochthonous origin. Additionally, reverse transcription quantitative polymerase chain reaction (RT-qPCR) was performed to detect WNV nucleic acid in horse sera and was found to be negative in all cases. Risk factor analysis did not identify any factors significantly associated with seropositivity.
Department of Mathematics University of Salzburg Hellbrunner Straße 34 5020 Salzburg Austria
Institute for Vertebrate Biology Czech Academy of Sciences Kvĕtná 8 60365 Brno Czech Republic
Citace poskytuje Crossref.org
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