Analyze Diet
Interdisciplinary perspectives on infectious diseases2010; 2010; 709791; doi: 10.1155/2010/709791

Animal models of CNS viral disease: examples from borna disease virus models.

Abstract: Borna disease (BD), caused by the neurotropic RNA virus, Borna Disease virus, is an affliction ranging from asymptomatic to fatal meningoencephalitis across naturally and experimentally infected warmblooded (mammalian and bird) species. More than 100 years after the first clinical descriptions of Borna disease in horses and studies beginning in the 1980's linking Borna disease virus to human neuropsychiatric diseases, experimentally infected rodents have been used as models for examining behavioral, neuropharmacological, and neurochemical responses to viral challenge at different stages of life. These studies have contributed to understanding the role of CNS viral injury in vulnerability to behavioral, developmental, epileptic, and neurodegenerative diseases and aided evaluation of the proposed and still controversial links to human disease.
Publication Date: 2010-02-24 PubMed ID: 20204069PubMed Central: PMC2829629DOI: 10.1155/2010/709791Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research discusses how rodent models infected with Borna Disease virus have been used to understand behavioural, neurochemical, and neuropharmacological responses at different life stages, therefore, aiding in the understanding of viral injury’s role in behavioural, developmental, epileptic, and neurodegenerative diseases.

Overview of Borna Disease Virus

  • Borna disease (BD), an affliction caused by Borna Disease virus, a neurotropic RNA virus, can range from asymptomatic to fatal meningoencephalitis.
  • This disease affects both mammalian and bird species that are naturally and experimentally infected.
  • The disease was first clinically described in horses over a century ago and has been linked to human neuropsychiatric diseases since the 1980s.

Use of Animal Models

  • Rodents have been experimentally infected as models to examine behavioral, neuropharmacological, and neurochemical responses at different stages of life.
  • The results from these animal model studies contribute to the understanding of the role of CNS viral injury in various diseases.

Contribution to Behavioral, Epileptic, and Neurodegenerative Diseases Comprehension

  • The research on rodent models infected by Borna Disease virus has improved understanding of the role of CNS viral injuries in vulnerability to behavioral, developmental, epileptic, and neurodegenerative disorders.
  • Such research is vital in developing effective treatments and preventative measures.

Controversial Links to Human Disease

  • The study also examines controversial proposals linking Borna Disease virus to human disease.
  • The outcomes from such explorations can help shape future research and inform strategies to address these diseases.

Cite This Article

APA
Solbrig MV. (2010). Animal models of CNS viral disease: examples from borna disease virus models. Interdiscip Perspect Infect Dis, 2010, 709791. https://doi.org/10.1155/2010/709791

Publication

ISSN: 1687-7098
NlmUniqueID: 101496545
Country: Egypt
Language: English
Volume: 2010
Pages: 709791
PII: 709791

Researcher Affiliations

Solbrig, Marylou V
  • Department of Internal Medicine (Neurology) and Medical Microbiology, University of Manitoba, Winnipeg, MB, Canada R3A 1R9.

Grant Funding

  • R01 NS042307 / NINDS NIH HHS

References

This article includes 64 references
  1. Rott R, Herzog S, Fleischer B, Winokur A, Amsterdam J, Dyson W, Koprowski H. Detection of serum antibodies to Borna disease virus in patients with psychiatric disorders.. Science 1985 May 10;228(4700):755-6.
    pubmed: 3922055doi: 10.1126/science.3922055google scholar: lookup
  2. Bode L, Riegel S, Ludwig H, Amsterdam JD, Lange W, Koprowski H. Borna disease virus-specific antibodies in patients with HIV infection and with mental disorders.. Lancet 1988 Sep 17;2(8612):689.
    pubmed: 2901550doi: 10.1016/s0140-6736(88)90505-3google scholar: lookup
  3. Zwick W. Borna’sche krankheit und encephalomyelitis der tiere. Handbuch der Viruskrankheiten Vol. 2. Jena, Germany: Fischer; 1939. pp. 252–354.
  4. Ludwig H, Thein P. Demonstration of specific antibodies in the central nervous system of horses naturally infected with Borna disease virus.. Med Microbiol Immunol 1977 Dec 27;163(4):215-26.
    pubmed: 604728doi: 10.1007/bf02125505google scholar: lookup
  5. Waelchli RO, Ehrensperger F, Metzler A, Winder C. Borna disease in a sheep.. Vet Rec 1985 Nov 9;117(19):499-500.
    pubmed: 4082400doi: 10.1136/vr.117.19.499google scholar: lookup
  6. Ludwig H, Bode L, Gosztonyi G. Borna disease: a persistent virus infection of the central nervous system.. Prog Med Virol 1988;35:107-51.
    pubmed: 3051132
  7. Solbrig MV, Fallon JH, Lipkin WI. Behavioral disturbances and pharmacology of Borna disease.. Curr Top Microbiol Immunol 1995;190:93-101.
    pubmed: 7789152doi: 10.1007/978-3-642-78618-1_6google scholar: lookup
  8. Nitzschke E. Investigation about the experimental Bornavirus-infection in the rat. Journal of Veterinary Medicine B 1963;10:470–527.
  9. Narayan O, Herzog S, Frese K, Scheefers H, Rott R. Behavioral disease in rats caused by immunopathological responses to persistent borna virus in the brain.. Science 1983 Jun 24;220(4604):1401-3.
    pubmed: 6602380doi: 10.1126/science.6602380google scholar: lookup
  10. Narayan O, Herzog S, Frese K, Scheefers H, Rott R. Pathogenesis of Borna disease in rats: immune-mediated viral ophthalmoencephalopathy causing blindness and behavioral abnormalities.. J Infect Dis 1983 Aug;148(2):305-15.
    pubmed: 6604114doi: 10.1093/infdis/148.2.305google scholar: lookup
  11. Hirano N, Kao M, Ludwig H. Persistent, tolerant or subacute infection in Borna disease virus-infected rats.. J Gen Virol 1983 Jul;64 (Pt 7):1521-30.
    pubmed: 6408221doi: 10.1099/0022-1317-64-7-1521google scholar: lookup
  12. Dittrich W, Bode L, Ludwig H, Kao M, Schneider K. Learning deficiencies in Borna disease virus-infected but clinically healthy rats.. Biol Psychiatry 1989 Dec;26(8):818-28.
    pubmed: 2511930doi: 10.1016/0006-3223(89)90122-4google scholar: lookup
  13. Rubin SA, Waltrip RW 2nd, Bautista JR, Carbone KM. Borna disease virus in mice: host-specific differences in disease expression.. J Virol 1993 Jan;67(1):548-52.
    pmc: PMC237392pubmed: 8416380doi: 10.1128/jvi.67.1.548-552.1993google scholar: lookup
  14. Stitz L, Krey H, Ludwig H. Borna disease in rhesus monkeys as a models for uveo-cerebral symptoms.. J Med Virol 1981;6(4):333-40.
    pubmed: 7241097doi: 10.1002/jmv.1890060408google scholar: lookup
  15. Sprankel H, Richarz K, Ludwig H, Rott R. Behavior alterations in tree shrews (Tupaia glis, Diard 1820) induced by Borna disease virus.. Med Microbiol Immunol 1978 May 26;165(1):1-18.
    pubmed: 566371doi: 10.1007/bf02121228google scholar: lookup
  16. Lipkin WI, Briese T. Bornaviridae. Field’s Virology 5th edition. Vol. 2. Philadelphia, Pa, USA: Lippincott Williams & Wilkins; 2007. pp. 1829–1851.
  17. . From animals to man--50 years of development. Proceedings of the International Berlin Symposium on Bornavirus Infections. January 26-28, 2008. Berlin, Germany.. APMIS Suppl 2008;(124):3-97.
    pubmed: 18828206
  18. Solbrig MV, Koob GF. Neuropharmacological sequelae of persistent CNS viral infections: lessons from Borna disease virus.. Pharmacol Biochem Behav 2003 Mar;74(4):777-87.
    pubmed: 12667891doi: 10.1016/s0091-3057(03)00019-4google scholar: lookup
  19. Solbrig MV, Koob GF, Fallon JH, Lipkin WI. Tardive dyskinetic syndrome in rats infected with Borna disease virus.. Neurobiol Dis 1994 Dec;1(3):111-9.
    pubmed: 9173990doi: 10.1006/nbdi.1994.0014google scholar: lookup
  20. Gosztonyi G, Ludwig H. Borna disease--neuropathology and pathogenesis.. Curr Top Microbiol Immunol 1995;190:39-73.
    pubmed: 7789150
  21. Solbrig MV, Koob GF, Lipkin WI. Cocaine sensitivity in Borna disease virus-infected rats.. Pharmacol Biochem Behav 1998 Apr;59(4):1047-52.
    pubmed: 9586866doi: 10.1016/s0091-3057(97)00507-8google scholar: lookup
  22. Solbrig MV, Koob GF, Parsons LH, Kadota T, Horscroft N, Briese T, Lipkin WI. Neurotrophic factor expression after CNS viral injury produces enhanced sensitivity to psychostimulants: potential mechanism for addiction vulnerability.. J Neurosci 2000 Nov 1;20(21):RC104.
  23. Solbrig MV, Koob GF, Joyce JN, Lipkin WI. A neural substrate of hyperactivity in borna disease: changes in brain dopamine receptors.. Virology 1996 Aug 15;222(2):332-8.
    pubmed: 8806517doi: 10.1006/viro.1996.0430google scholar: lookup
  24. Solbrig MV, Koob GF, Fallon JH, Reid S, Lipkin WI. Prefrontal cortex dysfunction in Borna disease virus (BDV)--infected rats.. Biol Psychiatry 1996 Oct 1;40(7):629-36.
    pubmed: 8886296doi: 10.1016/0006-3223(95)00480-7google scholar: lookup
  25. Gies U, Bilzer T, Stitz L, Staiger JF. Disturbance of the cortical cholinergic innervation in Borna disease prior to encephalitis.. Brain Pathol 1998 Jan;8(1):39-48.
  26. Gies U, Görcs TJ, Mulder J, Planz O, Stitz L, Bilzer T, Luiten PG, Harkany T. Cortical cholinergic decline parallels the progression of Borna virus encephalitis.. Neuroreport 2001 Dec 4;12(17):3767-72.
  27. Bautista JR, Schwartz GJ, De La Torre JC, Moran TH, Carbone KM. Early and persistent abnormalities in rats with neonatally acquired Borna disease virus infection.. Brain Res Bull 1994;34(1):31-40.
    pubmed: 8193931doi: 10.1016/0361-9230(94)90183-xgoogle scholar: lookup
  28. Hornig M, Weissenböck H, Horscroft N, Lipkin WI. An infection-based model of neurodevelopmental damage.. Proc Natl Acad Sci U S A 1999 Oct 12;96(21):12102-7.
    pmc: PMC18419pubmed: 10518583doi: 10.1073/pnas.96.21.12102google scholar: lookup
  29. Pletnikov MV, Moran TH, Carbone KM. Borna disease virus infection of the neonatal rat: developmental brain injury model of autism spectrum disorders.. Front Biosci 2002 Mar 1;7:d593-607.
    pubmed: 11861216doi: 10.2741/a797google scholar: lookup
  30. Weissenböck H, Hornig M, Hickey WF, Lipkin WI. Microglial activation and neuronal apoptosis in Bornavirus infected neonatal Lewis rats.. Brain Pathol 2000 Apr;10(2):260-72.
  31. Pletnikov MV, Rubin SA, Schwartz GJ, Carbone KM, Moran TH. Effects of neonatal rat Borna disease virus (BDV) infection on the postnatal development of the brain monoaminergic systems.. Brain Res Dev Brain Res 2000 Feb 7;119(2):179-85.
    pubmed: 10675767doi: 10.1016/s0165-3806(99)00168-6google scholar: lookup
  32. Pletnikov MV, Rubin SA, Vogel MW, Moran TH, Carbone KM. Effects of genetic background on neonatal Borna disease virus infection-induced neurodevelopmental damage. II. Neurochemical alterations and responses to pharmacological treatments.. Brain Res 2002 Jul 19;944(1-2):108-23.
    pubmed: 12106671doi: 10.1016/s0006-8993(02)02724-5google scholar: lookup
  33. Dietz D, Vogel M, Rubin S, Moran T, Carbone K, Pletnikov M. Developmental alterations in serotoninergic neurotransmission in Borna disease virus (BDV)-infected rats: a multidisciplinary analysis.. J Neurovirol 2004 Oct;10(5):267-77.
    pubmed: 15385249doi: 10.1080/13550280490499506google scholar: lookup
  34. Eisenman LM, Brothers R, Tran MH, Kean RB, Dickson GM, Dietzschold B, Hooper DC. Neonatal Borna disease virus infection in the rat causes a loss of Purkinje cells in the cerebellum.. J Neurovirol 1999 Apr;5(2):181-9.
    pubmed: 10321982doi: 10.3109/13550289909022000google scholar: lookup
  35. Pletnikov MV, Rubin SA, Moran TH, Carbone KM. Exploring the cerebellum with a new tool: neonatal Borna disease virus (BDV) infection of the rat's brain.. Cerebellum 2003;2(1):62-70.
    pubmed: 12882236doi: 10.1080/14734220309425google scholar: lookup
  36. Williams BL, Lipkin WI. Endoplasmic reticulum stress and neurodegeneration in rats neonatally infected with borna disease virus.. J Virol 2006 Sep;80(17):8613-26.
    pmc: PMC1563873pubmed: 16912310doi: 10.1128/jvi.00836-06google scholar: lookup
  37. Williams BL, Yaddanapudi K, Kirk CM, Soman A, Hornig M, Lipkin WI. Metallothioneins and zinc dysregulation contribute to neurodevelopmental damage in a model of perinatal viral infection.. Brain Pathol 2006 Jan;16(1):1-14.
  38. Williams BL, Yaddanapudi K, Hornig M, Lipkin WI. Spatiotemporal analysis of purkinje cell degeneration relative to parasagittal expression domains in a model of neonatal viral infection.. J Virol 2007 Mar;81(6):2675-87.
    pmc: PMC1865998pubmed: 17182680doi: 10.1128/jvi.02245-06google scholar: lookup
  39. Williams BL, Hornig M, Yaddanapudi K, Lipkin WI. Hippocampal poly(ADP-Ribose) polymerase 1 and caspase 3 activation in neonatal bornavirus infection.. J Virol 2008 Feb;82(4):1748-58.
    pmc: PMC2258717pubmed: 18057239doi: 10.1128/jvi.02014-07google scholar: lookup
  40. Pletnikov MV, Jones ML, Rubin SA, Moran TH, Carbone KM. Rat model of autism spectrum disorders. Genetic background effects on Borna disease virus-induced developmental brain damage.. Ann N Y Acad Sci 2001 Jun;939:318-9.
    pubmed: 11462786
  41. Avishai-Eliner S, Brunson KL, Sandman CA, Baram TZ. Stressed-out, or in (utero)?. Trends Neurosci 2002 Oct;25(10):518-24.
  42. Ovanesov MV, Moldovan K, Smith K, Vogel MW, Pletnikov MV. Persistent Borna Disease Virus (BDV) infection activates microglia prior to a detectable loss of granule cells in the hippocampus.. J Neuroinflammation 2008 May 19;5:16.
    pmc: PMC2397384pubmed: 18489759doi: 10.1186/1742-2094-5-16google scholar: lookup
  43. Sauder C, de la Torre JC. Cytokine expression in the rat central nervous system following perinatal Borna disease virus infection.. J Neuroimmunol 1999 Apr 1;96(1):29-45.
    pubmed: 10227422doi: 10.1016/s0165-5728(98)00272-0google scholar: lookup
  44. Plata-Salamán CR, Ilyin SE, Gayle D, Romanovitch A, Carbone KM. Persistent Borna disease virus infection of neonatal rats causes brain regional changes of mRNAs for cytokines, cytokine receptor components and neuropeptides.. Brain Res Bull 1999 Aug;49(6):441-51.
    pubmed: 10483922doi: 10.1016/s0361-9230(99)00081-7google scholar: lookup
  45. Sauder C, Hallensleben W, Pagenstecher A, Schneckenburger S, Biro L, Pertlik D, Hausmann J, Suter M, Staeheli P. Chemokine gene expression in astrocytes of Borna disease virus-infected rats and mice in the absence of inflammation.. J Virol 2000 Oct;74(19):9267-80.
  46. Hooper DC, Ohnishi ST, Kean R, Numagami Y, Dietzschold B, Koprowski H. Local nitric oxide production in viral and autoimmune diseases of the central nervous system.. Proc Natl Acad Sci U S A 1995 Jun 6;92(12):5312-6.
    pmc: PMC41684pubmed: 7539914doi: 10.1073/pnas.92.12.5312google scholar: lookup
  47. Hooper DC, Kean RB, Scott GS, Spitsin SV, Mikheeva T, Morimoto K, Bette M, Röhrenbeck AM, Dietzschold B, Weihe E. The central nervous system inflammatory response to neurotropic virus infection is peroxynitrite dependent.. J Immunol 2001 Sep 15;167(6):3470-7.
    pubmed: 11544340doi: 10.4049/jimmunol.167.6.3470google scholar: lookup
  48. Gonzalez-Dunia D, Watanabe M, Syan S, Mallory M, Masliah E, De La Torre JC. Synaptic pathology in Borna disease virus persistent infection.. J Virol 2000 Apr;74(8):3441-8.
  49. Köster-Patzlaff C, Hosseini SM, Reuss B. Loss of connexin36 in rat hippocampus and cerebellar cortex in persistent Borna disease virus infection.. J Chem Neuroanat 2009 Mar;37(2):118-27.
  50. Kamitani W, Shoya Y, Kobayashi T, Watanabe M, Lee BJ, Zhang G, Tomonaga K, Ikuta K. Borna disease virus phosphoprotein binds a neurite outgrowth factor, amphoterin/HMG-1.. J Virol 2001 Sep;75(18):8742-51.
  51. Diamond A. Rate of maturation of the hippocampus and the developmental progression of children's performance on the delayed non-matching to sample and visual paired comparison tasks.. Ann N Y Acad Sci 1990;608:394-426; discussion 426-33.
  52. Plata-Salamán CR, Ilyin SE, Gayle D, Romanovitch A, Carbone KM. Persistent Borna disease virus infection of neonatal rats causes brain regional changes of mRNAs for cytokines, cytokine receptor components and neuropeptides.. Brain Res Bull 1999 Aug;49(6):441-51.
    pubmed: 10483922doi: 10.1016/s0361-9230(99)00081-7google scholar: lookup
  53. Thorsell A, Michalkiewicz M, Dumont Y, Quirion R, Caberlotto L, Rimondini R, Mathé AA, Heilig M. Behavioral insensitivity to restraint stress, absent fear suppression of behavior and impaired spatial learning in transgenic rats with hippocampal neuropeptide Y overexpression.. Proc Natl Acad Sci U S A 2000 Nov 7;97(23):12852-7.
    pmc: PMC18853pubmed: 11058155doi: 10.1073/pnas.220232997google scholar: lookup
  54. Kamitani W, Ono E, Yoshino S, Kobayashi T, Taharaguchi S, Lee BJ, Yamashita M, Kobayashi T, Okamoto M, Taniyama H, Tomonaga K, Ikuta K. Glial expression of Borna disease virus phosphoprotein induces behavioral and neurological abnormalities in transgenic mice.. Proc Natl Acad Sci U S A 2003 Jul 22;100(15):8969-74.
    pmc: PMC166422pubmed: 12857949doi: 10.1073/pnas.1531155100google scholar: lookup
  55. Rauer M, Götz J, Schuppli D, Staeheli P, Hausmann J. Transgenic mice expressing the nucleoprotein of Borna disease virus in either neurons or astrocytes: decreased susceptibility to homotypic infection and disease.. J Virol 2004 Apr;78(7):3621-32.
  56. Hausmann J, Hallensleben W, de la Torre JC, Pagenstecher A, Zimmermann C, Pircher H, Staeheli P. T cell ignorance in mice to Borna disease virus can be overcome by peripheral expression of the viral nucleoprotein.. Proc Natl Acad Sci U S A 1999 Aug 17;96(17):9769-74.
    pmc: PMC22285pubmed: 10449769doi: 10.1073/pnas.96.17.9769google scholar: lookup
  57. Kao M, Ludwig H, Gosztonyi G. Adaptation of Borna disease virus to the mouse.. J Gen Virol 1984 Oct;65 ( Pt 10):1845-9.
    pubmed: 6436435doi: 10.1099/0022-1317-65-10-1845google scholar: lookup
  58. Hallensleben W, Schwemmle M, Hausmann J, Stitz L, Volk B, Pagenstecher A, Staeheli P. Borna disease virus-induced neurological disorder in mice: infection of neonates results in immunopathology.. J Virol 1998 May;72(5):4379-86.
  59. Sauder C, Hallensleben W, Pagenstecher A, Schneckenburger S, Biro L, Pertlik D, Hausmann J, Suter M, Staeheli P. Chemokine gene expression in astrocytes of Borna disease virus-infected rats and mice in the absence of inflammation.. J Virol 2000 Oct;74(19):9267-80.
  60. Sauder C, Wolfer DP, Lipp HP, Staeheli P, Hausmann J. Learning deficits in mice with persistent Borna disease virus infection of the CNS associated with elevated chemokine expression.. Behav Brain Res 2001 May;120(2):189-201.
    pubmed: 11182167doi: 10.1016/s0166-4328(00)00370-3google scholar: lookup
  61. Sauder C, Herpfer I, Hässler C, Staeheli P. Susceptibility of Borna disease virus to the antiviral action of gamma-interferon: evidence for species-specific differences.. Arch Virol 2004 Nov;149(11):2171-86.
    pubmed: 15503205doi: 10.1007/s00705-004-0360-5google scholar: lookup
  62. Stögmann E, Zimprich A, Baumgartner C, Aull-Watschinger S, Höllt V, Zimprich F. A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy.. Ann Neurol 2002 Feb;51(2):260-3.
    pubmed: 11835385doi: 10.1002/ana.10108google scholar: lookup
  63. Simonato M, Romualdi P. Dynorphin and epilepsy.. Prog Neurobiol 1996 Dec;50(5-6):557-83.
    pubmed: 9015827doi: 10.1016/s0301-0082(96)00045-7google scholar: lookup
  64. Solbrig MV, Adrian R, Baratta J, Lauterborn JC, Koob GF. Kappa opioid control of seizures produced by a virus in an animal model.. Brain 2006 Mar;129(Pt 3):642-54.
    pubmed: 16399805doi: 10.1093/brain/awl008google scholar: lookup

Citations

This article has been cited 8 times.
  1. Widerspick L, Steffen JF, Tappe D, Muñoz-Fontela C. Animal Model Alternatives in Filovirus and Bornavirus Research.. Viruses 2023 Jan 4;15(1).
    doi: 10.3390/v15010158pubmed: 36680198google scholar: lookup
  2. Castro E Silva JH, Souza JT, Schitine C, Júnior AFS, Bastos EMS, Costa SL. Pharmacological Potential of Flavonoids against Neurotropic Viruses.. Pharmaceuticals (Basel) 2022 Sep 15;15(9).
    doi: 10.3390/ph15091149pubmed: 36145370google scholar: lookup
  3. Schlottau K, Feldmann F, Hanley PW, Lovaglio J, Tang-Huau TL, Meade-White K, Callison J, Williamson BN, Rosenke R, Long D, Wylezich C, Höper D, Herden C, Scott D, Hoffmann D, Saturday G, Beer M, Feldmann H. Development of a nonhuman primate model for mammalian bornavirus infection.. PNAS Nexus 2022 Jul;1(3):pgac073.
    doi: 10.1093/pnasnexus/pgac073pubmed: 35860599google scholar: lookup
  4. Hopkins HK, Traverse EM, Barr KL. Methodologies for Generating Brain Organoids to Model Viral Pathogenesis in the CNS.. Pathogens 2021 Nov 19;10(11).
    doi: 10.3390/pathogens10111510pubmed: 34832665google scholar: lookup
  5. He P, Sun L, Zhu D, Zhang H, Zhang L, Guo Y, Liu S, Zhou J, Xu X, Xie P. Knock-Down of Endogenous Bornavirus-Like Nucleoprotein 1 Inhibits Cell Growth and Induces Apoptosis in Human Oligodendroglia Cells.. Int J Mol Sci 2016 Mar 24;17(4):435.
    doi: 10.3390/ijms17040435pubmed: 27023521google scholar: lookup
  6. Liu X, Bode L, Zhang L, Wang X, Liu S, Zhang L, Huang R, Wang M, Yang L, Chen S, Li Q, Zhu D, Ludwig H, Xie P. Health care professionals at risk of infection with Borna disease virus - evidence from a large hospital in China (Chongqing).. Virol J 2015 Mar 12;12:39.
    doi: 10.1186/s12985-015-0239-ypubmed: 25888756google scholar: lookup
  7. Smeal RM, Stewart KA, Iacob E, Fujinami RS, White HS, Wilcox KS. The activity within the CA3 excitatory network during Theiler's virus encephalitis is distinct from that observed during chronic epilepsy.. J Neurovirol 2012 Feb;18(1):30-44.
    doi: 10.1007/s13365-012-0082-5pubmed: 22328242google scholar: lookup
  8. Rackova S, Janu L, Kabickova H. Borna disease virus (BDV) circulating immunocomplex positivity in addicted patients in the Czech Republic: a prospective cohort analysis.. BMC Psychiatry 2010 Sep 8;10:70.
    doi: 10.1186/1471-244X-10-70pubmed: 20825673google scholar: lookup