Literature DB >> 6090697

Genetic basis of the neurovirulence of pseudorabies virus.

B Lomniczi, S Watanabe, T Ben-Porat, A S Kaplan.   

Abstract

Lomniczi et al. (J. Virol. 49:970-979, 1984) have shown previously that two attenuated vaccine strains of pseudorabies virus have a similar deletion in the short unique (US) region of the genome. The region which is deleted normally codes for several translationally competent mRNAs. As expected, these mRNAs are not formed in the cells infected with the vaccine strains. The function specified by these mRNAs is thus not necessary for growth in cell culture. Using intracerebral inoculation of 1-day-old chicks as a test system, we have attempted to determine whether a gene within the region that is missing from the attenuated strains specifies functions that are required for the expression of virulence. An analysis of recombinants between the Bartha vaccine strain and a virulent pseudorabies virus strain (having or lacking a thymidine kinase gene [TK+ or TK-]) revealed the following. None of the recombinant plaque isolates that were either TK- or which had a deletion in the US was virulent. Not all recombinant plaque isolates which were both TK+ and had an intact US were virulent. These results indicate that both thymidine kinase activity and an intact US were necessary but not sufficient for the expression of virulence. Marker rescue experiments involving cotransfection of the Bartha strain DNA and a restriction fragment spanning the region of the genome that was missing from the Bartha strain resulted in the isolation of virions to which an intact US had been restored. These virions were not virulent but had an improved ability to replicate in the brains of chicks compared with that of the parental nonrescued Bartha strain. Our results show that genes in the US region, which are missing from the Bartha strain, were necessary for virulence but that this strain was also defective in other genes required for the expression of virulence. Thus, the virulence of pseudorabies virus, as measured by intracerebral inoculation into chicks, appears to be controlled multigenically.

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Year:  1984        PMID: 6090697      PMCID: PMC254506     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  28 in total

1.  Herpes simplex virus thymidine kinase expression in infection of the trigeminal ganglion.

Authors:  R B Tenser; M E Dunstan
Journal:  Virology       Date:  1979-12       Impact factor: 3.616

2.  Structural evolution of the DNA of pseudorabies-defective viral particles.

Authors:  F J Rixon; T Ben-Porat
Journal:  Virology       Date:  1979-08       Impact factor: 3.616

3.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

4.  Characterization of defective interfering viral particles present in a population of pseudorabies virions.

Authors:  T Ben-Porat; J M Demarchi; A S Kaplan
Journal:  Virology       Date:  1974-09       Impact factor: 3.616

5.  Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.

Authors:  P S Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

6.  Cell-free translation of early and late mRNAs selected by hybridization to cloned DNA fragments derived from the left 14 million to 72 million daltons of the vaccinia virus genome.

Authors:  H B Isle; S Venkatesan; B Moss
Journal:  Virology       Date:  1981-07-15       Impact factor: 3.616

7.  Thymidine-kinase in cytomegalovirus infected cells.

Authors:  V Závada; V Erban; D Rezácová; V Vonka
Journal:  Arch Virol       Date:  1976       Impact factor: 2.574

8.  Resistance of peripheral autonomic neurons to in vivo productive infection by herpes simplex virus mutants deficient in thymidine kinase activity.

Authors:  R W Price; A Khan
Journal:  Infect Immun       Date:  1981-11       Impact factor: 3.441

9.  Biological characterization of a herpes simplex virus intertypic recombinant which is completely and specifically non-neurovirulent.

Authors:  R L Thompson; J G Stevens
Journal:  Virology       Date:  1983-11       Impact factor: 3.616

10.  Localization of the regions of homology between the genomes of herpes simplex virus, type 1, and pseudorabies virus.

Authors:  T Ben-Porat; R A Veach; S Ihara
Journal:  Virology       Date:  1983-05       Impact factor: 3.616

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  49 in total

1.  Role of a structural glycoprotein of pseudorabies in virus virulence.

Authors:  T C Mettenleiter; L Zsak; A S Kaplan; T Ben-Porat; B Lomniczi
Journal:  J Virol       Date:  1987-12       Impact factor: 5.103

2.  Neuron-to-cell spread of pseudorabies virus in a compartmented neuronal culture system.

Authors:  T H Ch'ng; L W Enquist
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

3.  Restriction fragment pattern analysis of genomes from French isolates of suis herpes virus 1 (Aujeszky's disease virus).

Authors:  A Jestin; P Blanchard; A Garbar-Chenon; P Vannier; J C Nicolas
Journal:  Arch Virol       Date:  1990       Impact factor: 2.574

4.  Role of pseudorabies virus glycoprotein gI in virus release from infected cells.

Authors:  T C Mettenleiter; C Schreurs; F Zuckermann; T Ben-Porat
Journal:  J Virol       Date:  1987-09       Impact factor: 5.103

5.  Analysis in vitro of two biologically distinct strains of murine cytomegalovirus.

Authors:  J B Hudson; D G Walker; M Altamirano
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

6.  Characterization of virulent and attenuated strains of pseudorabies virus for thymidine kinase activity, virulence and restriction patterns.

Authors:  M D McFarland; H T Hill; L B Tabatabai
Journal:  Can J Vet Res       Date:  1987-07       Impact factor: 1.310

7.  Insertions in the gG gene of pseudorabies virus reduce expression of the upstream Us3 protein and inhibit cell-to-cell spread of virus infection.

Authors:  G L Demmin; A C Clase; J A Randall; L W Enquist; B W Banfield
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

8.  Complementation analysis of pseudorabies virus gE and gI mutants in retinal ganglion cell neurotropism.

Authors:  L W Enquist; J Dubin; M E Whealy; J P Card
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

9.  Efficient incorporation of tegument proteins pUL46, pUL49, and pUS3 into pseudorabies virus particles depends on the presence of pUL21.

Authors:  Kathrin Michael; Barbara G Klupp; Axel Karger; Thomas C Mettenleiter
Journal:  J Virol       Date:  2006-11-01       Impact factor: 5.103

10.  Pseudorabies virus infection alters neuronal activity and connectivity in vitro.

Authors:  Kelly M McCarthy; David W Tank; Lynn W Enquist
Journal:  PLoS Pathog       Date:  2009-10-30       Impact factor: 6.823

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