Calisher CH, Childs JE, Field HE, Holmes KV, Schountz T. Bats: important reservoir hosts of emerging viruses. Clin Microbiol Rev. 2006;19:531–45.
Article
Google Scholar
Amarasinghe GK, Ayllon MA, Bao Y, Basler CF, Bavari S, Blasdell KR, Briese T, Brown PA, Bukreyev A, Balkema-Buschmann A, et al. Taxonomy of the order Mononegavirales: update 2019. Arch Virol. 2019;164:1967–80.
Article
CAS
Google Scholar
Korn K, Coras R, Bobinger T, Herzog SM, Lucking H, Stohr R, Huttner HB, Hartmann A, Ensser A. Fatal encephalitis associated with Borna disease virus 1. N Engl J Med. 2018;379:1375–7.
Article
Google Scholar
Schlottau K, Forth L, Angstwurm K, Hoper D, Zecher D, Liesche F, Hoffmann B, Kegel V, Seehofer D, Platen S, et al. Fatal encephalitic Borna disease virus 1 in solid-organ transplant recipients. N Engl J Med. 2018;379:1377–9.
Article
Google Scholar
Kolodziejek J, Dürrwald R, Herzog S, Ehrensperger F, Lussy H, Nowotny N. Genetic clustering of Borna disease virus natural animal isolates, laboratory and vaccine strains strongly reflects their regional geographical origin. J Gen Virol. 2005;86:385–98.
Article
CAS
Google Scholar
Weissenbock H, Bago Z, Kolodziejek J, Hager B, Palmetzhofer G, Durrwald R, Nowotny N. Infections of horses and shrews with Bornaviruses in Upper Austria: a novel endemic area of Borna disease. Emerg Microbes Infect. 2017;6:e52.
Article
Google Scholar
Dürrwald R, Kolodziejek J, Muluneh A, Herzog S, Nowotny N. Epidemiological pattern of classical Borna disease and regional genetic clustering of Borna disease viruses point towards the existence of to-date unknown endemic reservoir host populations. Microbes Infect. 2006;8:917–29.
Article
Google Scholar
Hilbe M, Herrsche R, Kolodziejek J, Nowotny N, Zlinszky K, Ehrensperger F. Shrews as reservoir hosts of Borna disease virus. Emerg Infect Dis. 2006;12:675–7.
Article
Google Scholar
Bourg M, Herzog S, Encarnacao JA, Nobach D, Lange-Herbst H, Eickmann M, Herden C. Bicolored white-toothed shrews as reservoir for Borna disease virus, Bavaria, Germany. Emerg Infect Dis. 2013;19:2064–6.
Article
Google Scholar
Kinnunen PM, Inkeroinen H, Ilander M, Kallio ER, Heikkilä HP, Koskela E, Mappes T, Palva A, Vaheri A, Kipar A, Vapalahti O. Intracerebral Borna disease virus infection of Bank voles leading to peripheral spread and reverse transcription of viral RNA. PLoS One. 2011;6:e23622.
Article
CAS
Google Scholar
Kinnunen PM, Billich C, Ek-Kommonen C, Henttonen H, Kallio RK, Niemimaa J, Palva A, Staeheli P, Vaheri A, Vapalahti O. Serological evidence for Borna disease virus infection in humans, wild rodents and other vertebrates in Finland. J Clin Virol. 2007;38:64–9.
Article
Google Scholar
Puorger ME, Hilbe M, Muller JP, Kolodziejek J, Nowotny N, Zlinszky K, Ehrensperger F. Distribution of Borna disease virus antigen and RNA in tissues of naturally infected bicolored white-toothed shrews, Crocidura leucodon, supporting their role as reservoir host species. Vet Pathol. 2010;47:236–44.
Article
CAS
Google Scholar
Nobach D, Bourg M, Herzog S, Lange-Herbst H, Encarnacao JA, Eickmann M, Herden C. Shedding of infectious Borna disease Virus-1 in living bicolored white-toothed shrews. PLoS One. 2015;10:e0137018.
Article
Google Scholar
Omatsu T, Watanabe S, Akashi H, Yoshikawa Y. Biological characters of bats in relation to natural reservoir of emerging viruses. Comp Immunol Microbiol Infect Dis. 2007;30:357–74.
Article
Google Scholar
Han HJ, Wen HL, Zhou CM, Chen FF, Luo LM, Liu JW, Yu XJ. Bats as reservoirs of severe emerging infectious diseases. Virus Res. 2015;205:1–6.
Article
CAS
Google Scholar
Plowright RK, Eby P, Hudson PJ, Smith IL, Westcott D, Bryden WL, Middleton D, Reid PA, McFarlane RA, Martin G, et al. Ecological dynamics of emerging bat virus spillover. Proc Biol Sci. 2015;282:20142124.
Article
Google Scholar
International Union for Conservation of Nature and nature Resources (IUCN): The IUCN Red List of Threatened Species. 2013 Available online: http://www.iucnredlist.org/. Accessed 27 June 2019).
Kohl C, Kurth A. European bats as carriers of viruses with zoonotic potential. Viruses. 2014;6:3110–28.
Article
Google Scholar
Haupt H, Ludwig G, Gruttke H, Binot-Hafke M, Otto C, Pauly A: Rote Liste gefährdeter Tiere, Pflanzen und Pilze Deutschlands Band 1: Wirbeltiere. Naturschutz und Biologische Vielfalt 70 (1) edn. Bonn - Bad Godesberg: Bundesamt für Naturschutz; 2009.
Smith PG, Racey PA. The itinerant Natterer: physical and therman characteristics of summer roosts Myotis nattereri (Mammalia: Chiroptera). J Zool. 2005;266:171–80.
Article
Google Scholar
Cui J, Wang LF. Genomic mining reveals deep evolutionary relationships between Bornaviruses and bats. Viruses. 2015;7:5792–800.
Article
CAS
Google Scholar
Horie M, Kobayashi Y, Honda T, Fujino K, Akasaka T, Kohl C, Wibbelt G, Muhldorfer K, Kurth A, Muller MA, et al. An RNA-dependent RNA polymerase gene in bat genomes derived from an ancient negative-strand RNA virus. Sci Rep. 2016;6:25873.
Article
CAS
Google Scholar
Mukai Y, Horie M, Tomonaga K. Systematic estimation of insertion dates of endogenous bornavirus-like elements in vesper bats. J Vet Med Sci. 2018;80(8):1356-63. https://doi.org/10.1292/jvms.18-0211.
Article
CAS
Google Scholar
Dacheux L, Cervantes-Gonzalez M, Guigon G, Thiberge JM, Vandenbogaert M, Maufrais C, Caro V, Bourhy H. A preliminary study of viral metagenomics of French bat species in contact with humans: identification of new mammalian viruses. PLoS One. 2014;9:e87194.
Article
Google Scholar
Belyi VA, Levine AJ, Skalka AM. Unexpected inheritance: multiple integrations of ancient bornavirus and ebolavirus/marburgvirus sequences in vertebrate genomes. PLoS Pathog. 2010;6:e1001030.
Article
Google Scholar
Horie M, Honda T, Suzuki Y, Kobayashi Y, Daito T, Oshida T, Ikuta K, Jern P, Gojobori T, Coffin JM, Tomonaga K. Endogenous non-retroviral RNA virus elements in mammalian genomes. Nature. 2010;463:84–7.
Article
CAS
Google Scholar
Horie M. The biological significance of bornavirus-derived genes in mammals. Curr Opin Virol. 2017;25:1–6.
Article
CAS
Google Scholar
Muhldorfer K, Speck S, Wibbelt G. Diseases in free-ranging bats from Germany. BMC Vet Res. 2011;7:61.
Article
Google Scholar
Bourg M, Nobach D, Herzog S, Lange-Herbst H, Nesseler A, Hamann HP, Becker S, Hoper D, Hoffmann B, Eickmann M, Herden C. Screening red foxes (Vulpes vulpes) for possible viral causes of encephalitis. Virol J. 2016;13:151.
Article
Google Scholar
Piepenbring AK, Enderlein D, Herzog S, Kaleta EF, Heffels-Redmann U, Ressmeyer S, Herden C, Lierz M. Pathogenesis of avian bornavirus in experimentally infected cockatiels. Emerg Infect Dis. 2012;18:234–41.
Article
Google Scholar
Hoffmann B, Tappe D, Hoper D, Herden C, Boldt A, Mawrin C, Niederstrasser O, Muller T, Jenckel M, van der Grinten E, et al. A variegated squirrel Bornavirus associated with fatal human encephalitis. N Engl J Med. 2015;373:154–62.
Article
CAS
Google Scholar
Werner-Keišs N, Garten W, Richt JA, Porombka D, Algermissen D, Herzog S, Baumgärtner W, Herden C. Restricted expression of Borna disease virus glycoprotein in brains of experimentally infected Lewis rats. Neuropathol Appl Neurobiol. 2008;34:590–602.
Article
Google Scholar
Fereidouni S, Kwasnitschka L, Balkema Buschmann A, Muller T, Freuling C, Schatz J, Pikula J, Bandouchova H, Hoffmann R, Ohlendorf B, et al. No virological evidence for an influenza a - like virus in European bats. Zoonoses Public Health. 2015;62:187–9.
Article
CAS
Google Scholar
VSG C, Jovanovic J, Siljic M, Paunovic M, Stanojevic M. Failure to detect viral RNA in bat samples collected in the Balkan region. Trop Biomed. 2016;33:780–5.
Google Scholar
Kurth A, Kohl C, Brinkmann A, Ebinger A, Harper JA, Wang LF, Muhldorfer K, Wibbelt G. Novel paramyxoviruses in free-ranging European bats. PLoS One. 2012;7:e38688.
Article
CAS
Google Scholar
Schindler AR, Vögtlin A, Hilbe M, Puorger M, Zlinszky K, Ackermann M, Ehrensperger F. Reverse transcription real-time PCR assays for detection and quantification of Borna disease virus in diseased hosts. Mol Cell Probes. 2007;21:47–55.
Article
CAS
Google Scholar
Hyndman TH, Shilton CM, Stenglein MD, Wellehan JFX Jr. Divergent bornaviruses from Australian carpet pythons with neurological disease date the origin of extant Bornaviridae prior to the end-cretaceous extinction. PLoS Pathog. 2018;14:e1006881.
Article
Google Scholar
Horie M, Tomonaga K. Paleovirology of bornaviruses: what can be learned from molecular fossils of bornaviruses. Virus Res. 2019;262:2–9.
Article
CAS
Google Scholar
Schneider U, Naegele M, Staeheli P, Schwemmle M. Active Borna disease virus polymerase complex requires a distinct nucleoprotein-to-phosphoprotein ratio but no viral X protein. J Virol. 2003;77:11781–9.
Article
CAS
Google Scholar