Detection of adeno-associated virus 2 and parvovirus B19 in the human dorsolateral prefrontal cortex

References

• Altschul S F, Madden T L, et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 1997; 25: 3389–3402, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 4th ed. American Psychiatric Association, Washington, DC 2000, text revision
   Google Scholar
• Balfour H H, Schiff G M, et al. Encephalitis associated with erythema infectiosum. J Pediatr 1970; 77: 133–136, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Bakhshi S, Sarnaik S A, et al. Acute encephalopathy with parvovirus B19 infection in sickle cell disease. Arch Dis Child 2002; 87: 541–542, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Barah F, Vallely P J, et al. Association of human parvovirus B19 infection with acute meningoencephalitis. Lancet 2001; 358: 729–730, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Barah F, Vallely P J, et al. Neurological manifestations of human parvovirus B19 infection. Rev Med Virol 2003; 13: 185–199, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Bilge I, Sadikoglu B, et al. Central nervous system vasculitis secondary to parvovirus B19 infection in a pediatric renal transplant patient. Pediatr Nephrol 2005; 20: 529–533, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Brown K E, Anderson S M, et al. Erythrocyte P antigen: cellular receptor for B19 parvovirus. Science 1993; 262: 114–117, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Bruemmer A, Scholari F, et al. Structure of an insect parvovirus (Junonia coenia densovirus) determined by cryo-electron microscopy. J Mol Biol 2005; 347: 791–801, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Buka S L, Tsuang M T, et al. Maternal infections and subsequent psychosis among offspring. Arch Gen Psychiatry 2001; 58: 1032–1037, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Burger C, Nash K, et al. Recombinant adeno-associated viral vectors in the nervous system. Hum Gene Ther 2005; 16: 781–791, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Cassinotti P, Burtonboy G, et al. Evidence for persistence of human parvovirus B19 DNA in bone marrow. J Med Virol 1997; 53: 229–232, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Druschky K, Walloch J, et al. Chronic parvovirus B-19 meningoencephalitis with additional detection of Epstein-Barr virus DNA in the cerebrospinal fluid of an immuncompetent patient. J Neuro Virol 2000; 6: 418–422, [CSA]
   Web of Science ®Google Scholar
• Erles K, Sebokova P, et al. Update on the prevalence of serum antibodies (IgG and IgM) to adeno-associated virus (AAV). J Med Virol 1999; 59: 406–411, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Farkas S L, Zadori Z, et al. A parvovirus isolated from royal python (Python regius) is a member of the genus dependovirus. J Gen Virol 2004; 85: 555–561, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Gao G, Vandenberghe L H, et al. Clades of adeno-associated viruses are widely disseminated in human tissues. J Virol 2004; 78: 6381–6388, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Gao G, Vandenberghe L H, et al. New recombinant serotypes of AAV vectors. Curr Gene Ther 2005; 5: 285–297, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Hadaczek P, Mirek H, et al. Basic fibroblast growth factor enhances transduction, distribution, and axonal transport of adeno-associated virus type 2 vector in rat brain. Hum Gene Ther 2004; 15: 469–479, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Heegaard E D, Brown K E. Human parvovirus B19. Clin Microbiol Rev 2002; 15: 485–505, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Heegaard E D, Peterslund N A, et al. Parvovirus B19 infection associated with encephalitis in a patient suffering from malignant lymphoma. Scand J Infect Dis 1995; 27: 631–633, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Hokynar K, Brunstein J, et al. Integrity and full coding sequence of B19 virus DNA persisting in human synovial tissue. J Gen Virol 2000; 81: 1017–1025, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Hsu D, Sandborg C, et al. Frontal lobe seizures and uveitis associated with acute human parvovirus B19 infection. J Child Neurol 2004; 19: 304–306, [INFOTRIEVE], [CSA]
   Google Scholar
• Hueffer K, Parrish C R. Parvovirus host range, cell tropism and evolution. Curr Opin Microbiol 2003; 6: 392–398, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Isumi H, Nunoue T, et al. Fetal brain infection with human parvovirus B19. Pediatr Neurol 1999; 21: 661–663, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Jarskog L F, Glantz L A, et al. Apoptotic mechanisms in the pathophysiology of schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2005; 29: 846–858, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Johnson R H, Margolis G, et al. Identity of feline ataxia virus with feline panleucopenia virus. Nature 1967; 217: 175–177, [CSA], [CROSSREF]
   Google Scholar
• Kaufmann B, Baxa U, et al. Parvovirus B19 does not bind to membrane-associated bloboside in vitro. Virology 2005; 332: 189–198, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Kerr J R. Pathogenesis of human parvovirus B19 in rheumatic disease. Ann Rheum Dis 2000; 59: 672–683, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Kerr J R, Barah F, et al. Evidence for the role of demyelination, HLA-DR alleles, and cytokines in the pathogenesis of parvovirus B19 meningoencephalitis and its sequelae. J Neurol Neurosurg Psychiatry 2002; 73: 739–746, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Kilham L. Mongolism associated with rat virus (RV) infection in hamsters. Virology 1961; 13: 141–143, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Kilham L, Margolis G. Problems of human concern arising from animal models of intrauterine and neonatal infections due to viruses: a review. Prog Med Virol 1975; 20: 113–179, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Koduri P R, Naides S J. Aseptic meningitis caused by parvovirus B19. Clin Infect Dis 1995; 27: 631–633, [CSA]
   Google Scholar
• Kotin R M, Linden R M, et al. Characterization of a preferred site on human chromosome 19q for integration of adeno-associated virus DNA by non-homologous recombination. EMBO J 1992; 11: 5071–5078, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Kuhl U, Pauschinger M, et al. Viral persistence in the myocardium is associated with progressive cardiac dysfunction. Circulation 2005; 112: 1965–1970, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Landauer K, Kilham L, et al. Behavioral characteristics associated with the rat-virus-induced “hamster mongolism” syndrome. J Psychiat Res 1967; 5: 95–106, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Manaye K F, Lei D L, et al. Selective neuron loss in the paraventricular neucleus of hypothalamus in patients suffering from major depression and bipolar disorder. J Neuropathol Exp Neurol 2005; 64: 224–229, [INFOTRIEVE], [CSA]
   Google Scholar
• Mandrioli J, Portolani M, et al. Middle cerebral artery thrombosis in course of parvovirus B19 infection in a young adult: a new risk factor for stroke?. J NeuroVirol 2004; 10: 71–74, [INFOTRIEVE], [CSA], [CROSSREF]
   Web of Science ®Google Scholar
• McCombie W R, Heiner C, et al. Rapid and reliable flouresent cycle sequencing of double stranded templates. DNA Sequence 1992; 2: 289–296, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Mortensen P B, Pedersen C B, et al. Effects of family history and place and season of birth on the risk of schizophrenia. N Engl J Med 1999; 340: 603–608, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Munakata Y, Saito-Ito T, et al. Ku80 autoantigen as a cellular coreceptor for human parvovirus B19 infection. Blood 2005; 106: 3449–3456, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Muzyczka N, Berns K I. Parvoviridae: the viruses and their replication. Field's virology, D M Knipe, P M Howley. Lippincott Williams & Wilkins, Philadelphia 2001; 2327–2359
   Google Scholar
• Nikkari S, Lappalainen H, et al. Detection of parvovirus B19 in skin biopsy, serum, and bone marrow of a patient with fever, rash, and polyarthritis followed by pneumonia, pericardial effusion, and hepatitis. Eur J Clin Microbiol Infect Dis 1996; 15: 954–957, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Nolan R C, Chidlow G, et al. Parvovirus B19 encephalitis presenting as immune restoration disease after highly active antiretroviral therapy for human immunodeficiency virus infection. Clin Infect Dis 2003; 36: 1191–1194, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Okumura A, Ichikawa T. Aseptic meningitis caused by human parvovirus B19. Arch Dis Child 1993; 68: 784–785, [INFOTRIEVE], [CSA]
   PubMedGoogle Scholar
• Qing K, Mah C, et al. Human fibroblast growth factor receptor 1 is a co-receptor for infection by adeno-associated virus 2. Nat Med 1999; 5: 71–77, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Ramirez J C, Fairen A, et al. Parvovirus minute virus of mice strain I multiplication and pathogenesis in the newborn mouse brain are restricted to proliferative areas and to migratory cerebellar young neurons. J Virol 1996; 70: 8109–8116, [INFOTRIEVE], [CSA]
   Google Scholar
• Sambrook J, Russell D W. Preparation of genomic DNA from mouse tails and other small samples. Alternative protocol: isolation of DNA from mouse tails without extraction by organic solvents. Molecular cloning: a laboratory manual, 3rd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York 2001; 6, 26
   Google Scholar
• Schennach H, Lanthaler A J, et al. Human parvovirus B19 detection in asymptomatic blood donors: associated with increased neopterin concentrations. J Infect Dis 2002; 186: 1494–1497, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Schnepp B C, Jensen R L, et al. Characterization of adeno-associated virus genomes isolated from human tissues. J Virol 2005; 79: 14793–14803, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Selemon L D, Rajkowska G. Cellular pathology in the dorsolateral prefrontal cortex distinguishes schizophrenia from bipolar disorder. Curr Mol Med 2003; 3: 427–436, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Shade R O, Blundell M C, et al. Nucleotide sequence and genome organization of human parvovirus B19 isolated from the serum of a child during aplastic crisis. J Virol 1986; 58: 921–936, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Shimizu Y, Ueno T, et al. Acute cerebellar ataxia with human parvovirus B19 infection. Arch Dis Child 1999; 80: 72–73, [INFOTRIEVE], [CSA]
   Google Scholar
• Skaff P T, Labiner D M. Status epilepticus due to human parvovirus B19 encephalitis in an immunocompetent adult. Neurology 2001; 57: 1336–1337, [INFOTRIEVE], [CSA]
   Google Scholar
• Smith L M, Sander J Z, et al. Flouresence detection in automated DNA sequence analysis. Nature 1986; 321: 674–679, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Song S, Embury J, Laipis P J, Berns K I, Crawford J M, Flotte T R. Stable therapeutic serum levels of human alpha-1 antitrypsin (AAT) after portal vein injection of recombinant adeno-associated virus (rAAV) vectors. Gene Ther 2001; 8: 1299–1306, [INFOTRIEVE], [CSA]
   Google Scholar
• Srivastava A, Lusby E W, et al. Nucleotide sequence and organization of the adeno-associated virus 2 genome. J Virol 1983; 45: 555–564, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Sukhumsirichart W, Attasart P, et al. Complete nucleotide sequence and genomic organization of hepatopancreatic parvovirus (HPV) of Panaeus monodon. Virology 2005; 346: 266–277, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Summerford C, Bartlett J S, et al. AlphaVbeta5 integrin: a co-receptor for adeno-associated virus type 2 infection. Nat Med 1999; 5: 78–82, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Summerford C, Samulski R J. Membrane-associated heparan sulfate proteoglycan is a receptor for adeno-asociated virus type 2 virions. J Virol 1998; 72: 1438–1445, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Tabak F, Mert A, et al. Prolonged fever caused by parvovirus B19-induced meningitis: case report and review. Clin Infect Dis 1999; 29: 446–447, [INFOTRIEVE], [CSA]
   Google Scholar
• Taller A M, Asher D M, et al. Search for viral nucleic acid sequences in brain tissues of patients with schizophrenia using nested polymerase chain reaction. Arch Gen Psychiatry 1996; 53: 32–40, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Thompson P M, Vidal C, et al. Mapping adolescent brain change reveals dynamic wave of accelerated gray matter loss in very early-onset schizophrenia. Proc Natl Acad Sci U S A 2001; 98: 11650–11655, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Tobiasch E, Burguete T, et al. Discrimination between different types of human adeno-associated viruses in clinical samples by PCR. J Virol Methods 1998; 71: 17–25, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Torok T J. Human Parvovirus B19. Infectious diseases of the fetus and newborn infant, J S Remington, J O Klein. W.B. Saunders, Philadelphia 2001; 779–811
   Google Scholar
• Torrey E F, Webster M J, et al. The Stanley Foundation Brain Collection and Neuropathology Consortium. Schizophr Res 2000; 44: 151–155, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Umene K, Nunoue T. A new genome type of human parvovirus B19 present in sera of patients with encephalopathy. J Gen Virol 1995; 76: 2645–2651, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Weigel-Kelley K A, Yoder M C, et al. α 5β 1 integrin as a cellular coreceptor for human parvovirus 19: requirement of functional activation of β 1 integrin for viral entry. Blood 2003; 102: 3927–3933, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Wierenga K J, Serjeant B E, et al. Cerebrovascular complications and parvovirus infection in homozygous sickle cell disease. J Pediatr 2001; 139: 438–442, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Woolf A D, Campion G V, et al. Clinical manifestations of human parvovirus B19 in adults. Arch Intern Med 1989; 149: 1153–1156, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMedGoogle Scholar
• Yolken R H, Torrey E F. Viruses, schizophrenia, and bipolar disorder. Clin Microbiol Rev 1995; 8: 131–145, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Yoto Y, Kudoh T, et al. Human parvovirus B19 and meningoencephalitis. Lancet 2001; 358: 2168, [INFOTRIEVE], [CSA], [CROSSREF]
   Google Scholar
• Young N S, Brown K E. Mechanisms of disease: parvovirus B19. N Engl J Med 2004; 350: 586–597, [INFOTRIEVE], [CSA], [CROSSREF]
   PubMed Web of Science ®Google Scholar
• Zhi N, Zadori Z, et al. Construction and sequencing of an infectious clone of the human parvovirus B19. Virology 2004; 31: 142–152, [CSA], [CROSSREF]
   Google Scholar