Differential anterograde transport of HSV type 1 viral strains in the murine optic pathway

References

• Burleson F G, Chambers T, Wiedbrauk D L. Virology: A Laboratory Manual. Academic Press, Inc., San Diego 1992
   Google Scholar
• Cook M L, Stevens J G. Pathogenesis of herpetic neuritis and ganglionitis in mice: Evidence for intra-axonal transport of infection. Inf Immun 1973; 7: 272–288
   PubMed Web of Science ®Google Scholar
• Davison A J, Elliot R M. Molecular Virology: a practical app roach. Oxford University Press, New York 1993; 315
   Google Scholar
• Dix R D, McKendall R R, Baringer J R. Comparative neurovirulence of herpes simplex virus type 1 strains after peripheral or intracerebral inoculation of BALB/c mice. Inf Immun 1983; 40: 103–112
   PubMed Web of Science ®Google Scholar
• Dobson A T, Margolis T P, Sedarati F, Stevens J G, Feldman L T. A latent, nonpathogenic HSV-1 derived vector stably expresses B-galactosidase in mouse neurons. Neuron 1990; 5: 353–360
   PubMed Web of Science ®Google Scholar
• Enquist L W, Husack P J, Banfield B W, Smith G A. Infection and spread of Alphaherpesviruses in the Nervous System. Advances in Virus Research 1998, in press
   Google Scholar
• Garner J A, Linse K D, Polk R K. Type I Brain hexokinase, axonal transport and membrane associations within central nervous system presynaptic terminals. J Neurochem 1996; 67: 845–856
   Google Scholar
• Gompels U, Minson A. The properties and sequence of glycoprotein H of herpes simplex type 1. Virol 1986; 153: 230–247
   PubMed Web of Science ®Google Scholar
• Haarr L, Skulstadt S. The herpes simplex virus type 1 protein structure and molecular functions. APMIS 1994; 102: 321–346
   Google Scholar
• Hamasaki D I, Rix R D, Atherton S S. Bilateral alterations of the ERG and retinal histology following unilateral HSV-1 inoculation. Invest Ophthalmol Vis Sci 1988; 29: 1242–1254
   Google Scholar
• Harlow E, Lane D. Antibodies: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY 1988
   Google Scholar
• Javier R T, Thompson R L, Stevens J G. Genetic and biological analyses of a herpes simplex virus inter-typic recombinant reduced specifically for neurovirulence. J Virol 1987; 61: 1978–1984
   Google Scholar
• Kistler H B, LaVail J H. Penetration of horseradish peroxidase into the optic nerve after vitreal or vascular injections in the developing chick. Invest Ophthalmol Vis Sci 1981; 20: 705–716
   Google Scholar
• Kristensson K, Ghetti B, Wisniewski H M. Study on the propagation of Herpes Simplex Virus (Type 2) into the brain after intraocular injection. Br Res 1974; 69: 189–201
   PubMedGoogle Scholar
• Kristensson K, Lycke E, Roytta M, Svennerholm B, Vahine A. Neuritic transport of herpes simplex virus in rat sensory neurons in vitro. Effects of substances interacting with microtubular function and axonal flow ‘Nocodazole, taxol, and erythro-9–3-(2-hydroxynonvl)adenine’. J Gen Virol 1986; 67: 2023–2028
   PubMed Web of Science ®Google Scholar
• LaVail J H, Nixon R A, Sidman R S. Genetic control of retinal ganglion cell projection. J Comp Neurol 1978; 182: 399–422
   PubMed Web of Science ®Google Scholar
• LaVail J H, Topp K S, Giblin P A, Garner J A. Factors that contribute to the efficiency of transneuronal spread of herpes simplex virus. J Neurosci Res 1997; 49: 485–496
   Google Scholar
• LaVail J H, Zhan J, Margolis T P. HSV (Type1) infection of the trigeminal complex. Br Res 1990; 514: 181–188
   PubMed Web of Science ®Google Scholar
• Lumb W W. Small Animal Anesthesia. Lea and Feibiger, Philadelphia, PA 1963
   Google Scholar
• Penfold M E T, Armati P, Cunningham A L. Axonal transport of herpes simplex virions to epidermal cells: Evidence for a specialized mode of virus transport and assembly. Proc Natl Acad Sci USA 1994; 91: 6529–6533
   Google Scholar
• Richards J T, Kern E R, Overall J C, Glasgow L A. Differences in neurovirulence among isolates of Herpes simplex virus types 1 and 2 in mice using four routes of infection. J Infect Dis 1981; 144: 464–471
   PubMed Web of Science ®Google Scholar
• Roizman B. Herpesviridae: a brief introduction. Fundamental Virology2nd ed., B N Fields, D M Knipe. Raven Press Ltd, New York 1991; 841–847
   Google Scholar
• Roizman B, Sears A E. Herpes simplex viruses and their replication. Virology2nd edn., B N Fields, D M Knipe. Raven Press, New York 1990; 1795–1841
   Google Scholar
• Sodeik B, Ebersold M W, Helenius A. Microtubule-mediated transport of incoming herpes simplex virus 1 capsids to the nucleus. J Cell Biol 1997; 136: 1007–1021
   PubMed Web of Science ®Google Scholar
• Steiner I, Kennedy P G. Herpes simplex virus latent infection in the nervous system. J Neurovirol 1995; 1: 19–29
   PubMed Web of Science ®Google Scholar
• Topp K S, Meade L B, La Vail J H. Microtubule polarity in the peripheral processes of trigeminal ganglion cells: Relevance for the retrograde transport of herpes simplex virus. J Neurosci 1994; 14: 318–325
   PubMed Web of Science ®Google Scholar
• Townsend J J. The relationship of astrocytes and macrophages to CNS demylination after experimental herpes simplex virus infection. J Neuropath Exp Neurol 1981; 40: 369–379
   PubMedGoogle Scholar
• Tso M O M, Shih C -Y, McLean I W. Is there a blood-brain barrier at the optic nerve head?. Arch Ophthalmol 1975; 93: 815–825
   PubMedGoogle Scholar
• Vallee R B, Bloom G S. Mechanisms of fast and slow axonal transport. Ann Rev Neurosci 1991; 14: 59–92
   PubMed Web of Science ®Google Scholar
• Whittum J A, McCulley J P, Niederkorn J Y, Streilein J W. Unilateral inoculation of herpes virus into the anterior chamber produces a bilateral uveitis with a pathogenesis potentially related to anterior chamber-associated immune deviation (ACAID). Advances in Immunology and Immumopathology of the Eye, G R O'Connor, J W Chandler. Masson Publishing, USA, Inc., New York 1985; 215–221
   Google Scholar
• Yuhasz S A, Stevens J G. Glycoprotein B is a specific determinant of herpes simplex virus type 1 neuroinvasiveness. J Virol 1993; 67: 5948–5954
   PubMed Web of Science ®Google Scholar
• Zemanick M C, Strick P L, Dix R D. Direction of transneuronal transport of herpes simplex virus 1 in the primate motor system is strain-dependent. Proc Natl Acad Sci USA 1991; 88: 8048–8051
   Google Scholar