Influence of infectious dose upon productive replication and transynaptic passage of pseudorabies virus in rat central nervous system

References

• Bartha. Experimental reduction if virulence of Aujeszky's disease virus. Magy. Allatorv Lapja 1961; 16: 43–45
   Google Scholar
• Becker. Zur primaren Schadingung vegetativer Ganglien nach Infektion mit dem Herpes suis virus bei verschiedenen Tierarten. Experentia 1967; 23: 209–217
   Google Scholar
• Card, Enquist. Use of pseudorabies virus for definition of synaptically linked populations of neurons. Methods Mol Genet 1994; 363–382
   Google Scholar
• Card, Enquist. Neurovirulence of pseudorabies virus. Critical Reviews in Neurobiology 1995, (in press)
   Google Scholar
• Card, Rinaman, Schwaber, Miselis, Whealy, Robbins, Enquist. Neurotropic properties of pseudorabies virus: uptake and transneuronal passage in the rat central nervous system. J Neurosci 1990; 10: 1974–1994
   PubMed Web of Science ®Google Scholar
• Card, Whealy, Robbins, Moore, Enquist. Two α-herpesvirus strains are transported differentially in the rodent visual system. Neuron 1991; 957–969
   Google Scholar
• Card, Whealy, Robbins, Enquist. Pseudorabies virus envelope glycoprotein gI influences both neurotropism and virulence during infection of the rat visual system. J Virol 1992; 66: 3032–3041
   Google Scholar
• Card, Rinaman, Lynn, Lee H, Meade, Miselis, Enquist. Pseudorabies virus infection of the rat central nervous system: ultrastructural characterization of viral replication, transport and pathogenesis. J Neurosci 1993; 13: 2515–2539
   PubMed Web of Science ®Google Scholar
• Carter, Pereira, Pax, La Vail. A quantitative assay of retrograde transported HSV in the trigeminal ganglion. Invest Ophthalmol Vis Sci 1992; 33: 1934–1939
   Google Scholar
• Dobbins, Feldman. Brainstem network controlling descending drive to phrenic motoneurons in rat. J Comp Neurol 1994; 347: 64–86
   Google Scholar
• Dolivo, Beretta, Bonifas, Foroglou. Ultrastructure and function in sympathetic ganglia isolated from rats infectd with pseudorabies virus. Brain Res 1978; 140: 111–123
   Google Scholar
• Enquist. Infection of the mammalian nervous system by pseudorabies virus (PRV). Semin Virol 1994; 221–231
   Google Scholar
• Enquist, Card. Pseudorabies virus: A tool for tracing neuronal connections and the responses of the CNS to neuronal infection. Gene Transfer into Postmitotic Neurones: Towards Gene Therapy of Human Neurological Disorders, Lowenstein, Enquist, 1995, (in press)
   Google Scholar
• Enquist, Dubin, Whealy, Card. Complementation analysis of pseudorabies virus gE and gI mutants in retinal ganglion cell neurotropism. J Virol 1994; 68: 5275–5279
   Google Scholar
• Jansen SP, Ter Horst, Mettenleiter, Loewy. CNS cell groups projecting to the submandibular parasympathetic preganglionic neurons in the rat: a retrograde transneuronal viral cell body labeling study. Brain Res 1992; 572: 253–260
   PubMed Web of Science ®Google Scholar
• Kuypers GJM, Ugolini. Viruses as transneuronal tracers. TINS 1990; 13: 71–75
   PubMed Web of Science ®Google Scholar
• Levine, Zhao S, Miselis. Direct and indirect retinohypothalamic projections to the supraoptic nucleus in the female albino rat. J Comp Neurol 1994; 341: 214–224
   Google Scholar
• Lomniczi, Watanabe, Ben-Porat, Kaplan. Genome location and identification of functions defective in the Bartha vaccine strain of pseudorabies virus. J Virol 1987; 61: 1796–801
   Google Scholar
• McLean, Nakane. Periodate-lysine-paraformaldehyde fixative. A new fixative for immunoelectron microscopy. J Histochem Cytochem 1974; 22: 1077–1083
   PubMed Web of Science ®Google Scholar
• Martin, Dolivo. Neuronal and transneuronal tracing in the trigeminal system of the rat using herpes virus suis. Brain Res 1983; 273: 253–276
   PubMed Web of Science ®Google Scholar
• Moore, Speh, Card. The retinohypothalamic tract originates from a distinct subset of retinal ganglion cells. J Comp Neurol 1995; 352: 351–366
   PubMed Web of Science ®Google Scholar
• Nadelhaft, Vera, Card, Miselis. Central nervous system neurons labeled following the injection of pseudorabies virus into the rat urinary bladder. Neurosci Lett 1992; 143: 271–274
   Google Scholar
• Rinaman, Card, Enquist. Spatiotemporal responses of astrocytes, ramified microglia, and brain macrophages to central neuronal infection with pseudorabies virus. J Neurosci 1993; 13: 685–702
   Google Scholar
• Robbins, Ryan, Whealy, Enquist. The gene encoding the gIII envelope glycoprotein of pseudorabies virus vaccine strain Bartha contains a mutation affecting protein localization. J Virol 1989; 63: 250–258
   Google Scholar
• Rock. The molecular basis of latent infections by alpha herpesviruses. Semin Virol 1993; 157–165
   Google Scholar
• Roizman. Herpesviridae: a brief introduction. Virology, Fields, Knipe, Chanock, Hirsch, Melnick, Monath, Roizman. Raven Press, New York 1990; 1787–1793
   Google Scholar
• Rotto-Percelay, Wheeler, Osorio, Platt, Loewy. Transneuronal labeling of spinal interneurons and sympathetic preganglionic neurons after pseudorabies virus injections in the rat medial gastrocnemius muscle. Brain Res 1992; 574: 291–306
   PubMed Web of Science ®Google Scholar
• Rouiller, Capt, Dolivo, De Ribaupierre. Tensor tympani reflex pathways studies horseradish peroxidase and transneuronal viral tracing techniques. Neurosci Lett 1986; 72: 247–252
   PubMed Web of Science ®Google Scholar
• Rouiller, Capt, Dolivo, De Ribaupierre. Neuronal organization of the stapedius reflex pathways in the rat: a retrograde HRP and viral transneuronal tracing study. Brain Res 1989; 476: 21–28
   PubMed Web of Science ®Google Scholar
• Schramm, Strack, Platt, Loewy. Peripheral and central pathways regulating the kidney: a study using pseudorabies virus. Brain Res 1993; 616: 251–262
   PubMed Web of Science ®Google Scholar
• Spencer, Sawyer, Wada, Platt, Loewy. CNS projections to the pterygopalatine parasympathetic preganglionic neurons in the rat: a retrograde transneuronal viral cell body labeling study. Brain Res 1990; 534: 149–169
   PubMed Web of Science ®Google Scholar
• Standish, Enquist, Schwaber. Innervation of the heart and its central medullary origin defined by viral tracing. Science 1994; 263: 232–234
   PubMedGoogle Scholar
• Standish, Enquist, Escardo, Schwaber. Central neuronal circuit innervating the rat heart defined by transneuronal transport of pseudorabies virus. J Neurosci 1995; 15: 1998–2012
   PubMed Web of Science ®Google Scholar
• Strack, Loewy. Pseudorabies virus: a highly specific transneuronal cell body marker in the sympathetic nervous system. J Neurosci 1990; 10: 2139–2147
   Google Scholar
• Strack, Sawyer, Platt, Loewy. CNS cell groups regulating the sympathetic outflow to adrenal gland as revealed by transneuronal cell body labeling with pseudorabies virus. Brain Res 1989a; 491: 274–296
   PubMed Web of Science ®Google Scholar
• Strack, Sawyer, Hughes, Platt, Loewy. A general pattern of CNS innervation of the sympathetic outflow demonstrated by transneuronal pseudorabies viral infections. Brain Res 1989b; 491: 156–162
   PubMed Web of Science ®Google Scholar
• Strick, Card. Transneuronal mapping of neural circuits with alpha herpesviruses. Experimental Neuroanatomy. A Practical Approach, Bolam. IRL Press, Oxford 1992; 81–101
   Google Scholar
• Ugolini, Kuypers GJM, Simmons. Retrograde transneuronal transfer of herpes simplex virus type 1 (HSV 1) from motoneurones. Brain Res 1987; 422: 242–256
   PubMed Web of Science ®Google Scholar
• Vizzard A., Erickson, Card, Roppolo, de Groat. Transneuronal labeling of neurons in the adult rat brainstem and spinal cord after injection of pseudorabies virus into the urethra. J Comp Neurol 1995; 355: 629–640
   PubMed Web of Science ®Google Scholar
• Whealy, Card, Robbins, Dubin, Rziha J, Enquist. Specific pseudrorabies virus infection of the rat visual system requires both gI and gp63 glycoproteins. J Virol 1993; 67: 3786–3797
   Google Scholar
• Zuckerman, Zsak, Mettenleiter, Ben-Porat. Pseudorabies virus glycoprotein gIII is a major target antigen for murine and swine virus-specific cytotoxic T lymphocytes. J Virol 1990; 64: 802–812
   Google Scholar