Mapping of herpes simplex virus-1 neurovirulence to gamma 134.5, a gene nonessential for growth in culture
- PMID: 2173860
- DOI: 10.1126/science.2173860
Mapping of herpes simplex virus-1 neurovirulence to gamma 134.5, a gene nonessential for growth in culture
Abstract
The gene designated gamma 134.5 maps in the inverted repeats flanking the long unique sequence of herpes simplex virus-1 (HSV-1) DNA, and therefore it is present in two copies per genome. This gene is not essential for viral growth in cell culture. Four recombinant viruses were genetically engineered to test the function of this gene. These were (i) a virus from which both copies of the gene were deleted, (ii) a virus containing a stop codon in both copies of the gene, (iii) a virus containing after the first codon an insert encoding a 16-amino acid epitope known to react with a specific monoclonal antibody, and (iv) a virus in which the deleted sequences were restored. The viruses from which the gene was deleted or which carried stop codons were avirulent on intracerebral inoculation of mice. The virus with the gene tagged by the sequence encoding the epitope was moderately virulent, whereas the restored virus reacquired the phenotype of the parent virus. Significant amounts of virus were recovered only from brains of animals inoculated with virulent viruses. Inasmuch as the product of the gamma 134.5 gene extended the host range of the virus by enabling it to replicate and destroy brain cells, it is a viral neurovirulence factor.
Similar articles
-
Herpes simplex virus type 1 deletion variants 1714 and 1716 pinpoint neurovirulence-related sequences in Glasgow strain 17+ between immediate early gene 1 and the 'a' sequence.J Gen Virol. 1991 Mar;72 ( Pt 3):631-9. doi: 10.1099/0022-1317-72-3-631. J Gen Virol. 1991. PMID: 1848598
-
Herpes simplex virus 1 mutant deleted in the alpha 22 gene: growth and gene expression in permissive and restrictive cells and establishment of latency in mice.J Virol. 1985 Aug;55(2):338-46. doi: 10.1128/JVI.55.2.338-346.1985. J Virol. 1985. PMID: 2991560 Free PMC article.
-
Replication, establishment of latency, and induced reactivation of herpes simplex virus gamma 1 34.5 deletion mutants in rodent models.J Clin Invest. 1993 Jun;91(6):2837-43. doi: 10.1172/JCI116527. J Clin Invest. 1993. PMID: 8390490 Free PMC article.
-
Mechanisms of restriction of viral gene expression during herpes simplex virus latency.Adv Exp Med Biol. 1990;278:211-7. doi: 10.1007/978-1-4684-5853-4_22. Adv Exp Med Biol. 1990. PMID: 1963037 Review. No abstract available.
-
[Molecular biology of pathogenesis by herpesvirus].Rev Latinoam Microbiol. 1991 Jan-Mar;33(1):77-85. Rev Latinoam Microbiol. 1991. PMID: 1670258 Review. Spanish.
Cited by
-
Persistent inflammation and neuronal loss in the mouse brain induced by a modified form of attenuated herpes simplex virus type I.Virol Sin. 2023 Feb;38(1):108-118. doi: 10.1016/j.virs.2022.11.008. Epub 2022 Nov 24. Virol Sin. 2023. PMID: 36436797 Free PMC article.
-
The herpes simplex virus 1 Us11 protein inhibits autophagy through its interaction with the protein kinase PKR.J Virol. 2013 Jan;87(2):859-71. doi: 10.1128/JVI.01158-12. Epub 2012 Oct 31. J Virol. 2013. PMID: 23115300 Free PMC article.
-
Blocking Autophagy in M1 Macrophages Enhances Virus Replication and Eye Disease in Ocularly Infected Transgenic Mice.J Virol. 2022 Nov 9;96(21):e0140122. doi: 10.1128/jvi.01401-22. Epub 2022 Oct 26. J Virol. 2022. PMID: 36286481 Free PMC article.
-
Asymptomatic Herpes Simplex Virus Type 1 Infection Causes an Earlier Onset and More Severe Experimental Autoimmune Encephalomyelitis.Front Immunol. 2021 Feb 15;12:635257. doi: 10.3389/fimmu.2021.635257. eCollection 2021. Front Immunol. 2021. PMID: 33679788 Free PMC article.
-
Identification of an African swine fever virus gene with similarity to a myeloid differentiation primary response gene and a neurovirulence-associated gene of herpes simplex virus.J Virol. 1992 Sep;66(9):5586-9. doi: 10.1128/JVI.66.9.5586-5589.1992. J Virol. 1992. PMID: 1323711 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical