Herpes simplex virus vector system: analysis of its in vivo and in vitro cytopathic effects

• Published in: Journal of neuroscience methods 1995-04, Vol.57 (2), p.205-215
• Main Authors: Ho, Dora Y., Fink, Sheri L., Lawrence, Matthew S., Meier, Timothy J., Saydam, Tippi C., Dash, Rajesh, Sapolsky, Robert M.
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Biotechnology; Cell Count; Cell Survival; Cells, Cultured; Corpus Striatum - virology; Cytopathic effect; Cytopathogenic Effect, Viral; DNA, Viral; Fundamental and applied biological sciences. Psychology; Gene Transfer Techniques; Gene transfer vector; Genetic engineering; Genetic technics; Genetic Vectors; Herpes simplex virus; Hippocampal culture; Hippocampus; Hippocampus - virology; In Vitro Techniques; Methods. Procedures. Technologies; Simplexvirus - genetics; Striatum; Vectors (cloning, transfer, expression). Insertion sequences and transposons
• ISSN: 0165-0270; 1872-678X
• DOI: 10.1016/0165-0270(94)00150-F

With its natural propensity to infect and establish life-long latency in neurons, herpes simplex virus type 1 (HSV-1) has been successfully employed by various laboratories as vectors for gene transfer into neurons. However, analysis of its cytopathic effects in vivo and in vitro has been limited. In this study, we examined the cytopathic effects of 2 HSV-1 α4 mutants (ts756 and d120) on adult rat hippocampus and striatum and of d120 on hippocampal neurons in culture. We assessed damage by stringent counting of surviving neurons after infection and demonstrated that while neither ts756 nor d120 infection resulted in any gross anatomical or behavioral changes of the animals, ts756, but not d120, produced a significant amount of damage in the CA4 cell field and dentate gyrus of the hippocampus. Thus, since crude examination is insufficient to detect subtle but significant degrees of neuron loss, the cytopathic effects of HSV or any vector system must be carefully analyzed. Furthermore, we also observed that uninfected cell lysates damaged neurons, both in vivo and in vitro. This cytotoxicity occurred within the first 24 h post-inoculation and probably arose through the activation of glutamate receptors. For the preparation of HSV vectors, purification of the virus from soluble cellular components by a simple pelleting step can significantly decrease such acute toxicity.