Herpes simplex virus replication hits a nerve

References

• Bataille D, Epstein A. Herpes simplex virus replicative concatomers contain L components in inverted orientation. Virology 1994; 203: 384–388
   Google Scholar
• Becker Y, Asher Y, Weinberg-Zahlering E, Rabkin S, Friedman A, Kessler E. Defective herpes simplex virus DNA: circular and circular linear molecules resembling rolling circles. J Gen Virol 1978; 40: 319–335
   Google Scholar
• Block T, Barney S, Masonis J, Maggioncalda, Rattan S, Vagi-Nagy T, Frazer N. Long-term herpes simplex virus infections of nerve growth factor differentiated PC12 cells. J Gen Virol 1994; 75: 2481–2487
   Google Scholar
• Chalberg M. Herpes simplex virus DNA replication. Semin Virol 1991; 2: 247–256
   Google Scholar
• Deshmane S L, Raengsakulrach B, Berson J F, Fraser N W. The replication intermediates of herpes simplex virus type 1 DNA are relatively short. J Neuro Virology 1995, (this issue)
   Google Scholar
• Diess L P, Frankel N. Herpes simplex virus amplicon: cleavage of concatemeric DNA is linked to packaging and involves amplification of the terminally reiterated a sequence. J Virol 1986; 57: 933–941
   Google Scholar
• Efstathiou S, Minson C, Field H J, Anderson J R, Wildly P. Detection of herpes simplex virus-specific DNA sequences in latently infected mice and humans. J Virol 1986; 57: 446–455
   PubMed Web of Science ®Google Scholar
• Fraser N, Block T, Spivack J. The latency associated transcripts of herpes simplex virus type 1: transcripts in search of a function. Virology 1992; 191: 1–8
   PubMed Web of Science ®Google Scholar
• Garber D A, Beverley S M, Coen D M. Demonstration of circularization of herpes simplex virus DNA following infection using pulse field gel electrophoresis. Virology 1993; 197: 459–462
   PubMed Web of Science ®Google Scholar
• Hayward G S, Jacob R J, Wadsworth S C, Roizman B. Anatomy of herpes simplex virus DNA: evidence for four populations of molecules that differ in their relative orientations of long and short segments. Proc Natl Acad Sci USA 1975; 72: 4243–4247
   PubMed Web of Science ®Google Scholar
• Henken D B, Goldstein M E, Zhang Q, Curtis R. Neuronal sprouting in mouse sensory ganglia infected with herpes simplex virus type 2 (HSV-2): induction and growth associated protein (GAP43) and ultrastructural evidence. J Neuro Virology 1995, (this issue)
   Google Scholar
• Jacob R J, Roizman B. Anatomy of herpes simplex virus DNA. VIII. Properties of the replicating DNA. J Virol 1979; 23: 394–411
   Google Scholar
• Jacob R J, Morse S L, Roizman B. Anatomy of herpes simplex virus DNA XII. Accumulation of head to tail concatemers in nuclei of infected cells and their role in the generation of the four isomeric arrangements of viral DNA. J. Virol 1979; 29: 448–457
   Google Scholar
• Jongeneel V C, Bachenheimer S L. Structure of replicating herpes simplex virus DNA. J Virol 1981; 39: 656–660
   Google Scholar
• McGeoch D J, Dalrymple M A, Davison A J, Dolan A, Frame M C, McNab D, Perry L J, Scott J E, Taylor P. The complete sequence of the long unique region in the genome of herpes simplex virus type 1. J Gen Virol 1988; 69: 1531–1574
   PubMed Web of Science ®Google Scholar
• Mellerick D M, Fraser N W. Physical state of the latent herpes simplex virus genome in a mouse model system: evidence suggesting an episomal state. Virology 1987; 158: 265–275
   PubMed Web of Science ®Google Scholar
• Mocarski E S, Roizman B. Structure and role of the herpes simplex virus DNA termini in inversion, circularization and generation of virion DNA. Cell 1982; 31: 89–97
   PubMedGoogle Scholar
• Rock D L, Fraser N W. Detection of HSV-1 genome in the central nervous system of latently infected mice. Nature 1983; 302: 523–525
   PubMed Web of Science ®Google Scholar
• Roizman B. The structure and isomerization of herpes simplex virus genomes. Cell 1989; 16: 481–494
   Google Scholar
• Severini A, Morgan A R, Tovell D R, Tyrell D IJ. Study of the structure of the replicative intermediates of HSV-1 DNA by pulse field gel electrophoresis. Virology 1994; 200: 428–436
   PubMed Web of Science ®Google Scholar
• Sheldrick P, Berthelot N. Inverted repetitions in the chromosome of herpes simplex virus. Cold Spring Harbor Symp Quant Biol 1975; 39: 667–678
   Google Scholar
• Skene J HP. Axonal growth associated proteins. Ann Rev Neurosci 1989; 12: 127–156
   PubMed Web of Science ®Google Scholar
• Stevens J G. Overview of herpesvirus latency. Semin Virol 1994; 5: 191–196
   Google Scholar
• Varmuza S L, Smiley J R. Signals for site specific cleavage of herpes simplex virus DNA: maturation involves two separate cleavage events at sites distal to the recognition sequences. Cell 1985; 41: 793–802
   Google Scholar
• Woolf C J, Shortland P, Coggeshall R E. Peripheral nerve injury triggers central sprouting of myelinated afferents. Nature 1992; 355: 75–78
   PubMed Web of Science ®Google Scholar
• Zhang X, Efsthathiou S, Simmons A. Identification of novel herpes simplex virus replicative intermediates by field inversion gel electrophoresis: implications for viral DNA amplification strategies. Virology 1994; 202: 530–539
   PubMed Web of Science ®Google Scholar