Literature DB >> 3003243

An in vitro latency system for herpes simplex virus type 2.

J Russell, C M Preston.   

Abstract

An in vitro latency system for herpes simplex virus type 2 (HSV-2) in cultured cells has been developed. Virus replication was suppressed by infection of human foetal lung cells at the supraoptimal temperature of 42 degrees C, and, following transfer of such cell cultures to the normal growth temperature of 37 degrees C, infectious virus was generally undetectable for at least 6 days. HSV-2 was reactivated by intertypic superinfection at 38.5 degrees C with temperature-sensitive mutants of HSV-1, or with human cytomegalovirus, but not by superinfection with adenovirus types 2 or 5. The HSV-1 mutant tsKsyn, which produces only immediate early polypeptides at 38.5 degrees C, was as effective as the late mutant tsIsyn, but tsK which had been irradiated with u.v. light to prevent gene expression did not reactivate HSV-2. The efficiency of reactivation was very high, since 15 to 34% of the theoretical input of infectious HSV-2 particles could be retrieved by superinfection with 0.3 p.f.u. of tsKsyn per cell. Reactivation of latent virus was not induced by cell subculture or by other treatments which alter cell metabolism. The system described here may be important for studies on the molecular basis of HSV latency.

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Year:  1986        PMID: 3003243     DOI: 10.1099/0022-1317-67-2-397

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  19 in total

1.  Abortive herpes simplex virus infection of nonneuronal cells results in quiescent viral genomes that can reactivate.

Authors:  Efrat M Cohen; Nir Avital; Meir Shamay; Oren Kobiler
Journal:  Proc Natl Acad Sci U S A       Date:  2019-12-23       Impact factor: 11.205

Review 2.  Current status review: molecular biology of herpes simplex virus latency.

Authors:  D S Latchman
Journal:  J Exp Pathol (Oxford)       Date:  1990-02

Review 3.  Human herpesviruses: a consideration of the latent state.

Authors:  J G Stevens
Journal:  Microbiol Rev       Date:  1989-09

4.  Human cytomegalovirus tegument protein pp71 directs long-term gene expression from quiescent herpes simplex virus genomes.

Authors:  Chris M Preston; Mary Jane Nicholl
Journal:  J Virol       Date:  2005-01       Impact factor: 5.103

5.  Attenuation of DNA-dependent protein kinase activity and its catalytic subunit by the herpes simplex virus type 1 transactivator ICP0.

Authors:  S P Lees-Miller; M C Long; M A Kilvert; V Lam; S A Rice; C A Spencer
Journal:  J Virol       Date:  1996-11       Impact factor: 5.103

6.  Macromolecular synthesis at the early stage of herpes simplex virus type 2 (HSV-2) latency in a human neuroblastoma cell line IMR-32: repression of late viral polypeptide synthesis and accumulation of cellular heat-shock proteins.

Authors:  Y Yura; K Terashima; H Iga; Y Kondo; T Yanagawa; H Yoshida; Y Hayashi; M Sato
Journal:  Arch Virol       Date:  1987       Impact factor: 2.574

7.  Human corneal cells and other fibroblasts can stimulate the appearance of herpes simplex virus from quiescently infected PC12 cells.

Authors:  Y H Su; R L Meegalla; R Chowhan; C Cubitt; J E Oakes; R N Lausch; N W Fraser; T M Block
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

8.  Herpes simplex virus type 1 persistence and latency in cultured rabbit corneal epithelial cells, keratocytes, and endothelial cells.

Authors:  S D Cook; S M Brown
Journal:  Br J Ophthalmol       Date:  1986-09       Impact factor: 4.638

Review 9.  Molecular biology of herpes simplex virus type 1 latency in the nervous system.

Authors:  I Steiner; P G Kennedy
Journal:  Mol Neurobiol       Date:  1993       Impact factor: 5.590

10.  Efficient quiescent infection of normal human diploid fibroblasts with wild-type herpes simplex virus type 1.

Authors:  Robert McMahon; Derek Walsh
Journal:  J Virol       Date:  2008-08-13       Impact factor: 5.103

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