Literature DB >> 1656073

The ability of pseudorabies virus to grow in different hosts is affected by the duplication and translocation of sequences from the left end of the genome to the UL-US junction.

L M Reilly1, G Rall, B Lomniczi, T C Mettenleiter, S Kuperschmidt, T Ben-Porat.   

Abstract

Pseudorabies virus is a herpesvirus which has a class 2 genome. However, under certain growth conditions it acquires a genome with class 3-like characteristics. In these variants, the leftmost sequences of the long (L) component of the viral genome have been duplicated and translocated to the right of the L component next to the short (S) component, resulting in an L component that is bracketed by inverted repeats. Consequently, the L component can invert and is found in two orientations relative to the S component. The translocation is accompanied invariably by a deletion of sequences that are normally present in the wild-type genome at the right end of the L component. The virion variants with an invertible L component have a growth advantage over wild-type virus in chicken embryo fibroblasts and chickens; they also have a growth disadvantage in mice or rabbit kidney cells. The changed growth characteristics of the variants reside entirely in the changed structure of the junction between the S and L components. Replacement of that region of the DNA with wild-type sequences restores the wild-type phenotype. To determine whether the modified growth characteristics of the variants are related to the translocation or to the deletion, mutants that have a deletion or that have a deletion as well as a translocation similar to those observed in the variants were constructed, and the growth characteristics of these mutants were determined. We show that the modified growth characteristics of the mutants with an invertible L component can be attributed to the translocation of the leftmost terminal sequences of the genome next to the inverted repeat; they are not related to the deletion of the sequences normally present at the right end of the L component. The translocation of the leftmost 325 bp of the genome is sufficient to confer upon the virus the modified cell-type-specific growth characteristics. Furthermore, the modified growth characteristics are contingent upon the presence of 68 bp spanning the internal junction between the L and S components.

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Year:  1991        PMID: 1656073      PMCID: PMC250246     

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


  22 in total

1.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

2.  Analysis of an origin of DNA replication located at the L terminus of the genome of pseudorabies virus.

Authors:  S Kupershmidt; J M DeMarchi; Z Q Lu; T Ben-Porat
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

3.  Structural organization of the termini of the L and S components of the genome of pseudorabies virus.

Authors:  J M DeMarchi; Z Q Lu; G Rall; S Kupershmidt; T Ben-Porat
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

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.  Sequence of the genome ends and of the junction between the ends in concatemeric DNA of pseudorabies virus.

Authors:  L Harper; J Demarchi; T Ben-Porat
Journal:  J Virol       Date:  1986-12       Impact factor: 5.103

6.  Deletions in the genomes of pseudorabies virus vaccine strains and existence of four isomers of the genomes.

Authors:  B Lomniczi; M L Blankenship; T Ben-Porat
Journal:  J Virol       Date:  1984-03       Impact factor: 5.103

7.  Characterization of a viable, noninverting herpes simplex virus 1 genome derived by insertion and deletion of sequences at the junction of components L and S.

Authors:  K L Poffenberger; E Tabares; B Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

8.  Replication of herpesvirus DNA. VI. Virions containing either isomer of pseudorabies virus DNA are infectious.

Authors:  T Ben-Porat; R A Veach; B F Ladin
Journal:  Virology       Date:  1980-04-30       Impact factor: 3.616

9.  Evolution of pseudorabies virions containing genomes with an invertible long component after repeated passage in chicken embryo fibroblasts.

Authors:  B Lomniczi; A Gielkens; I Csobai; T Ben-Porat
Journal:  J Virol       Date:  1987-06       Impact factor: 5.103

10.  Nucleotide sequences at recombinational junctions present in pseudorabies virus variants with an invertible L component.

Authors:  Z Q Lu; J M DeMarchi; L Harper; G F Rall; T Ben-Porat
Journal:  J Virol       Date:  1989-06       Impact factor: 5.103

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  5 in total

1.  Machinery to support genome segment inversion exists in a herpesvirus which does not naturally contain invertible elements.

Authors:  M A McVoy; D Ramnarain
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  A human cytomegalovirus deleted of internal repeats replicates with near wild type efficiency but fails to undergo genome isomerization.

Authors:  Anne Sauer; Jian Ben Wang; Gabriele Hahn; Michael A McVoy
Journal:  Virology       Date:  2010-03-07       Impact factor: 3.616

Review 3.  A Review of Pseudorabies Virus Variants: Genomics, Vaccination, Transmission, and Zoonotic Potential.

Authors:  Zongyi Bo; Xiangdong Li
Journal:  Viruses       Date:  2022-05-09       Impact factor: 5.818

4.  Acquisition of an additional internal cleavage site differentially affects the ability of pseudorabies virus to multiply in different host cells.

Authors:  G F Rall; Z Q Lu; N Sugg; R A Veach; T Ben-Porat
Journal:  J Virol       Date:  1991-12       Impact factor: 5.103

5.  Functions of the sequences at the ends of the inverted repeats of pseudorabies virus.

Authors:  G F Rall; S Kupershmidt; N Sugg; R A Veach; T Ben-Porat
Journal:  J Virol       Date:  1992-03       Impact factor: 5.103

  5 in total

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