Age-dependent development and clinical characteristics of an experimental parrot bornavirus-4 (PaBV-4) infection in cockatiels (Nymphicus hollandicus)

References

• Baur, K., Rauer, M., Richter, K., Pagenstecher, A., Götz, J., Hausmann, J. & Staeheli, P. (2008). Antiviral CD8 T cells recognize Borna disease virus antigen transgenically expressed in either neurons or astrocytes. Journal of Virology, 82, 3099–3108.
   PubMed Web of Science ®Google Scholar
• Bautista, J.R., Rubin, S.A., Moran, T.H., Schwartz, G.J. & Carbone, K.M. (1995). Developmental injury to the cerebellum following perinatal Borna disease virus infection. Developmental Brain Research, 90, 45–53.
   PubMedGoogle Scholar
• Bautista, J.R., Schwartz, G.J., de la Torre, J.C., Moran, T.H. & Carbone, K.M. (1994). Early and persistent abnormalities in rats with neonatally acquired Borna disease virus infection. Brain Research Bulletin, 34, 31–40.
   PubMed Web of Science ®Google Scholar
• Berhane, Y., Smith, D.A., Newman, S., Taylor, M., Nagy, E., Binnington, B. & Hunter, B. (2001). Peripheral neuritis in psittacine birds with proventricular dilatation disease. Avian Pathology, 30, 563–570.
   PubMed Web of Science ®Google Scholar
• Briese, T., Hornig, M. & Lipkin, W.I. (1999). Bornavirus immunopathogenesis in rodents: models for human neurological diseases. Journal of Neurovirology, 5, 604–612.
   PubMed Web of Science ®Google Scholar
• Carbone, K.M., Park, S.W., Rubin, S.A., Waltrip II, R.W. & Vogelsang, G.B. (1991). Borna disease: association with a maturation defect in the cellular immune response. Journal of Virology, 65, 6154–6164.
   PubMed Web of Science ®Google Scholar
• Dahlhausen, R.D. & Orosz, S.E. (2018, September). Avian bornaviral ganglioneuritis in clinical practice. In Proceedings of the annual association of avian veterinarians, exotics conference. e veterinary clinics of North America (Vol. 21, pp. 33–67). Exotic Animal Practice.
   Google Scholar
• De Kloet, S.R. & Dorrestein, G.M. (2009). Presence of avian bornavirus RNA and anti-avian bornavirus antibodies in apparently healthy macaws. Avian Diseases, 53, 568–573.
   PubMed Web of Science ®Google Scholar
• de la Torre, J.C. (2002). Bornavirus and the brain. Journal of Infectious Diseases, 186, 241–247.
   PubMed Web of Science ®Google Scholar
• Eisenman, L.M., Brothers, R., Tran, M.H., Kean, R.B., Dickson, G.M., Dietzschold, B. & Hooper, D.C. (1999). Neonatal Borna disease virus infection in the rat causes a loss of Purkinje cells in the cerebellum. Journal of NeuroVirology, 5, 181–189.
   PubMed Web of Science ®Google Scholar
• Encinas-Nagel, N., Enderlein, D., Piepenbring, A., Herden, C., Heffels-Redmann, U., Felippe, P.A., Arns, C., Hafez, H.M. & Lierz, M. (2014). Avian bornavirus in free-ranging psittacine birds, Brazil. Emerging Infectious Diseases, 20, 2103–2106.
   PubMed Web of Science ®Google Scholar
• Furrer, E., Bilzer, T., Stitz, L. & Planz, O. (2001). Neutralizing antibodies in persistent Borna disease virus infection: prophylactic effect of gp94-specific monoclonal antibodies in preventing encephalitis. Journal of Virology, 75, 943–951.
   PubMed Web of Science ®Google Scholar
• Gancz, A.Y., Kistler, A.L., Clubb, S., Skewes-Cox, P., Fischer, K., Sorber, K., Chiu, C.Y., Lublin, A., Mechani, S., Farnoushi, Y., Greninger, A., Wen, C.C., Karlene, S.B., Ganem, D. & Derisi, J.L. (2009). Divergent Borna viruses are associated with proventricular dilatation disease. Proceedings of the 10th European Association of Avian Veterinarians (EAAV) Annual Conference (pp. 147–154), Antwerpen.
   Google Scholar
• Gancz, A.Y., Kistler, A.L., Greninger, A.L., Farnoushi, Y., Mechani, S., Perl, S., Berkowitz, A., Perez, N., Clubb, S., DeRisi, J.L., Ganem, D. & Lublin, A. (2009). Experimental induction of proventricular dilatation disease in cockatiels (Nymphicus hollandicus) inoculated with brain homogenates containing avian bornavirus 4. Virology Journal, 6, 100.
   PubMed Web of Science ®Google Scholar
• Gray, P., Hoppes, S., Suchodolski, P., Mirhosseini, N., Payne, S., Villanueva, I., Shivaprasad, H.L., Honkavuori, K.S., Briese, T., Reddy, S.M. & Tizard, I. (2010). Use of avian bornavirus isolates to induce proventricular dilatation disease in conures. Emerging Infectious Diseases, 16, 473–479.
   PubMed Web of Science ®Google Scholar
• Hallensleben, W., Schwemmle, M., Hausmann, J., Stitz, L., Volk, B., Pagenstecher, A. & Staeheli, P. (1998). Borna disease virus-induced neurological disorder in mice: infection of neonates results in immunopathology. Journal of Virology, 72, 4379–4386.
   PubMed Web of Science ®Google Scholar
• Hameed, S.S., Guo, J., Tizard, I., Shivaprasad, H.L. & Payne, S. (2018). Studies on immunity and immunopathogenesis of parrot bornaviral disease in cockatiels. Virology, 515, 81–91.
   PubMed Web of Science ®Google Scholar
• Heckmann, J., Enderlein, D., Gartner, A.M., Bücking, B., Malberg, S., Herzog, S., Heffels-Redmann, U., Herden, C. & Lierz, M. (2017, March 25–29). Investigations of natural transmission routes of a parrot bornavirus-4 isolate (PaBV-4) in cockatiels. 3rd International Conference on Avian, Herpetological and Exotic Mammal Medicine (ICARE), Venice, Italy (pp. 656–657).
   Google Scholar
• Heffels-Redmann, U., Enderlein, D., Herzog, S., Herden, C., Piepenbring, A., Neumann, D., Müller, H., Capelli, S., Müller, H., Oberhäuser, K., Gerlach, H., Kaleta, E.F. & Lierz, M. (2011). Occurrence of avian bornavirus infection in captive psittacines in various European countries and its association with proventricular dilatation disease. Avian Pathology, 40, 419–426.
   PubMed Web of Science ®Google Scholar
• Herden, C., Herzog, S., Wehner, T., Zink, C., Richt, J.A. & Frese, K. (1999). Comparison of different methods of diagnosing Borna disease in horses post mortem. In U. Wernery, J. Wade, J.A. Mumford & O.R. Kaaden (Eds.), Equine Infectious Diseases 8th edn (pp. 286–290). Newmarket: R&W Publications.
   Google Scholar
• Herzog, S., Enderlein, D., Heffels-Redmann, U., Piepenbring, A., Neumann, D., Kaleta, E.F., Müller, H., Lierz, M. & Herden, C. (2010). Indirect immunofluorescence assay for intra vitam diagnosis of avian bornavirus infection in psittacine birds. Journal of Clinical Microbiology, 48, 2282–2284.
   PubMed Web of Science ®Google Scholar
• Herzog, S., Kompter, C., Frese, K. & Rott, R. (1984). Replication of Borna disease virus in rats: age-dependent differences in tissue distribution. Medical Microbiolgy and Immunology, 173, 171–177.
   PubMed Web of Science ®Google Scholar
• Hirano, N., Kao, M. & Ludwig, H. (1983). Persistent, tolerant or subacute infection in Borna disease virus-infected rats. Journal of General Virology, 64, 1521–1530.
   PubMed Web of Science ®Google Scholar
• Hoffmann, B., Tappe, D., Höper, D., Herden, C., Boldt, A., Mawrin, C., Niederstraßer, O., Müller, T., Jenckel, M., van der Grinten, E., Lutter, C., Abendroth, B., Teifke, J.P., Cadar, D., Schmidt-Chanasit, J., Ulrich, R.G. & Beer, M. (2015). A variegated squirrel bornavirus associated with fatal human encephalitis. New England Journal of Medicine, 373, 154–162.
   PubMed Web of Science ®Google Scholar
• Högemann, C., Richter, R., Korbel, R. & Rinder, M. (2017). Plasma protein, haematologic and blood chemistry changes in African grey parrots (Psittacus erithacus) experimentally infected with bornavirus. Avian Pathology, 46, 556–570.
   PubMed Web of Science ®Google Scholar
• Honkavuori, K.S., Shivaprasad, H.L., Williams, B.L., Quan, P.L., Hornig, M., Street, C., Palacios, G., Hutchison, S.K., Franca, M., Egholm, M., Briese, T. & Lipkin, W.I. (2008). Novel Borna virus in psittacine birds with proventricular dilatation disease. Emerging Infectious Diseases, 14, 1883–1886.
   PubMed Web of Science ®Google Scholar
• Hoppes, S., Gray, P.L., Payne, S., Shivaprasad, H.L. & Tizard, I. (2010). The isolation, pathogenesis, diagnosis, transmission, and control of avian bornavirus and proventricular dilatation disease. Veterinary Clinics of North America – Exotic Animal Practice, 13, 495–508.
   PubMedGoogle Scholar
• Hornig, M., Weissenböck, H., Horscroft, N. & Lipkin, W.I. (1999). An infection-based model of neurodevelopmental damage. Proceedings of the National Academy of Sciences of the United States of America, 96, 12102–12107.
   PubMed Web of Science ®Google Scholar
• Kerski, A., de Kloet, A.H. & de Kloet, S.R. (2012). Vertical transmission of avian bornavirus in Psittaciformes: avian bornavirus RNA and anti-avian bornavirus antibodies in eggs, embryos, and hatchlings obtained from infected sun conures (Aratinga solstitialis). Avian Diseases, 56, 471–478.
   PubMed Web of Science ®Google Scholar
• Kistler, A.L., Smith, J.M., Greninger, A.L., DeRisi, J.L. & Ganem, D. (2010). Analysis of naturally occurring avian bornavirus infection and transmission during an outbreak of proventricular dilatation disease among captive psittacine birds. Journal of Virology, 84, 2176–2179.
   PubMed Web of Science ®Google Scholar
• Lierz, M., Hafez, H.M., Honkavuori, K.S., Gruber, A.D., Olias, P., Abdelwhab, E.M., Kohls, A., Lipkin, W.I. & Briese, T. (2009). Anatomical distribution of ABV in parrots, its occurrence in clinical healthy birds and ABV-antibody detection. Avian Pathology, 38, 491–496.
   PubMed Web of Science ®Google Scholar
• Lierz, M., Herden, C., Herzog, S. & Piepenbring, A. (2010). Die neuropathische Drüsenmagendilatation der Psittaziden und das aviare Bornavirus als potenzielle Ursache. Tierarztliche Praxis Ausgabe K: Kleintiere – Heimtiere, 38, 87–94.
   PubMed Web of Science ®Google Scholar
• Lierz, M., Piepenbring, A., Herden, C., Oberhäuser, K., Heffels-Redmann, U. & Enderlein, D. (2011). Vertical transmission of avian bornavirus in psittacines. Emerging Infectious Diseases, 17, 2390–2391.
   PubMed Web of Science ®Google Scholar
• Mannl, A., Gerlach, H. & Leipold, R. (1987). Neuropathic gastric dilatation in Psittaciformes. Avian Diseases, 31, 214–221.
   PubMed Web of Science ®Google Scholar
• Mirhosseini, N., Gray, P.L., Hoppes, S., Tizard, I., Shivaprasad, H.L. & Payne, S. (2011). Proventricular dilatation disease in cockatiels (Nymphicus hollandicus) after infection with a genotype 2 avian bornavirus. Journal of Avian Medicine and Surgery, 25, 199–204.
   PubMed Web of Science ®Google Scholar
• Narayan, O., Herzog, S., Frese, K., Scheefers, H. & Rott, R. (1983a). Behavioral disease in rats caused by immunopathological responses to persistent Borna virus in the brain. Science, 220, 1401–1403.
   PubMed Web of Science ®Google Scholar
• Narayan, O., Herzog, S., Frese, K., Scheefers, H. & Rott, R. (1983b). Pathogenesis of Borna disease in rats: immune-mediated viral ophthalmoencephalopathy causing blindness and behavioral abnormalities. Journal of Infectious Diseases, 148, 305–315.
   PubMed Web of Science ®Google Scholar
• Nöske, K., Bilzer, T., Planz, O. & Stitz, L. (1998). Virus-specific CD4+ T cells eliminate Borna disease virus from the brain via induction of cytotoxic CD8+ T cells. Journal of Virology, 72, 4387–4395.
   PubMed Web of Science ®Google Scholar
• Piepenbring, A.K., Enderlein, D., Herzog, S., Al-Ibadi, B., Heffels-Redmann, U., Heckmann, J., Lange-Herbst, H., Herden, C. & Lierz, M. (2016). Parrot bornavirus (PaBV)-2 isolate causes different disease patterns in cockatiels than PaBV-4. Avian Pathology, 45, 156–168.
   PubMed Web of Science ®Google Scholar
• Piepenbring, A.K., Enderlein, D., Herzog, S., Kaleta, E.F., Heffels-Redmann, U., Ressmeyer, S., Herden, C. & Lierz, M. (2012). Pathogenesis of avian bornavirus in experimentally infected cockatiels. Emerging Infectious Diseases, 18, 234–241.
   PubMed Web of Science ®Google Scholar
• Planz, O. & Bilzer, T. (1995). Immunopathogenic role of T-cell subsets in Borna disease virus-induced progressive encephalitis. Journal of Virology, 69, 896–903.
   PubMed Web of Science ®Google Scholar
• Pletnikov, M.V., Moran, T.H. & Carbone, K.M. (2002). Borna disease virus infection of the neonatal rat: developmental brain injury model of autism spectrum disorders. BioScience, 1, 80–89.
   Google Scholar
• Pletnikov, M.V., Rubin, S.A., Schwartz, G.J., Moran, T.H., Sobotka, T.J. & Carbone, K.M. (1999). Persistent neonatal Borna disease virus (BDV) infection of the brain causes chronic emotional abnormalities in adult rats. Physiology & Behavior, 66, 823–831.
   PubMed Web of Science ®Google Scholar
• Raghav, R., Taylor, M., DeLay, J., Ojkic, D., Pearl, D.L., Kistler, A.L., DeRisi, J.L., Ganem, D. & Smith, D.A. (2010). Avian bornavirus is present in many tissues of psittacine birds with histopathologic evidence of proventricular dilatation disease. Journal of Veterinary Diagnostic Investigation, 22, 495–508.
   PubMed Web of Science ®Google Scholar
• Richt, J.A., Schmeel, A., Frese, K., Carbone, K.M., Narayan, O. & Rott, R. (1994). Borna disease virus-specific T cells protect against or cause immunopathological Borna disease. Journal of Experimental Medicine, 179, 1467–1473.
   PubMed Web of Science ®Google Scholar
• Rinder, M., Ackermann, A., Kempf, H., Kaspers, B., Korbel, R. & Staeheli, P. (2009). Broad tissue and cell tropism of avian bornavirus in parrots with proventricular dilatation disease. Journal of Virology, 83, 5401–5407.
   PubMed Web of Science ®Google Scholar
• Rott, R., Herzog, S., Richt, J. & Stitz, L. (1988). Immune-mediated pathogenesis of Borna disease. Zentralbl Bakteriol Mikrobiol Hyg A, 270, 295–301.
   PubMedGoogle Scholar
• Rubbenstroth, D., Brosinski, K., Rinder, M., Olbert, M., Kaspers, B., Korbel, R. & Staeheli, P. (2014). No contact transmission of avian bornavirus in experimentally infected cockatiels (Nymphicus hollandicus) and domestic canaries (Serinus canaria forma domestica). Veterinary Microbiology, 172, 146–156.
   PubMed Web of Science ®Google Scholar
• Rubin, S.A., Waltrip II, R.W., Bautista, J.R. & Carbone, K.M. (1993). Borna disease virus in mice: host-specific differences in disease expression. Journal of Virology, 67, 548–552.
   PubMed Web of Science ®Google Scholar
• Schlottau, K., Forth, L., Angstwurm, K., Höper, D., Zecher, D., Liesche, F., Hoffmann, B., Kegel, V., Seehofer, D., Platen, S., Salzberger, B., Liebert, U.G., Niller, H.-H., Schmidt, B., Matiasek, K., Riemenschneider, M.J., Brochhausen, C., Banas, B., Renders, L., Moog, P., Wunderlich, S., Seifert, C.L., Barreiros, A., Rahmel, A., Weiss, J., Tappe, D., Herden, C., Schmidt-Chanasit, J., Schwemmle, M., Rubbenstroth, D., Schlegel, J., Pietsch, C., Hoffmann, D., Jantsch, J., Beer, M. (2018). Fatal encephalitic Borna disease virus 1 in solid-organ transplant recipients. New England Journal of Medicine, 379, 1377–1379.
   PubMed Web of Science ®Google Scholar
• Seto, F. (1981, September 1). Early development of the avian immune system. Poultry Science, 60, 1981–1995.
   PubMed Web of Science ®Google Scholar
• Stitz, L., Bilzer, T. & Planz, O. (2002). The immunopathogenesis of Borna disease virus infection. Frontiers in Bioscience, 7, 541–555.
   Web of Science ®Google Scholar
• Stitz, L., Nöske, K., Planz, O., Furrer, E., Lipkin, W.I. & Bilzer, T. (1998). A functional role for neutralizing antibodies in Borna disease: influence on virus tropism outside the central nervous system. Journal of Virology, 72, 8884–8892.
   PubMed Web of Science ®Google Scholar
• Stitz, L., Soeder, D., Deschl, U., Frese, K. & Rott, R. (1989). Inhibition of immune-mediated meningoencephalitis in persistently Borna disease virus-infected rats by cyclosporine A. Journal of Immunology, 143, 4250–4256.
   PubMed Web of Science ®Google Scholar
• Watanabe, M., Lee, B.J., Kamitani, W., Kobayashi, T., Taniyama, H., Tomonaga, K. & Ikuta, K. (2001). Neurological diseases and viral dynamics in the brains of neonatally Borna disease virus-infected gerbils. Virology, 282, 65–76.
   PubMed Web of Science ®Google Scholar
• Watanabe, M., Lee, B.J., Yamashita, M., Kamitani, W., Kobayashi, T., Tomonaga, K. & Ikuta, K. (2003). Borna disease virus induces acute fatal neurological disorders in neonatal gerbils without virus- and immune-mediated cell destructions. Virology, 310, 245–253.
   PubMed Web of Science ®Google Scholar
• Wüst, E.M. (2017). Untersuchungen zur vertikalen Übertragung des Parrot Bornavirus bei Psittaziden (Dissertation). Justus Liebig University Gießen.
   Google Scholar