Literature DB >> 8002782

Pseudorabies virus infectivity for swine skin characterized in vitro.

E R Tulman1, A E Garmendia.   

Abstract

The infectivity of pseudorabies virus (PrV) was demonstrated in a cell substrate derived from swine skin explant cultures designated primary porcine skin cells (c/cSLA PPSC). c/cSLA PPSC infected with either wild type or TK- PrV strain Kaplan (Ka) developed typical cytopathologic changes (CPE) as early as 4 h post inoculation (p.i.). The CPE caused by PrV on c/cSLA PPSC was specifically neutralized by covalescent swine sera. Synthesis of late viral proteins was demonstrated in PrV-infected c/cSLA PPSC by indirect fluorescent antibody staining using monoclonal antibodies (mAbs) specific for PrV gIII. PrV induced protein synthesis was further confirmed by specific immunoprecipitation of 35S-methionine labeled viral polypeptides from PrV-infected c/cSLA PPSC with PrV convalescent swine serum, PrV immune mouse serum or mAb to PrV gIII. Moreover, the virus progeny derived from c/cSLA PPSC was shown to be infectious for MDBK cells and this infection was specifically neutralized by PrV convalescent swine serum. The capacity c/cSLA PPSC to support a complete growth cycle of PrV and the relative ease of deriving these cells from pigs can be applied in an autologous fashion in studies of cellular immunity where the MHC needs to be matched.

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Year:  1994        PMID: 8002782     DOI: 10.1007/BF01538824

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  28 in total

Review 1.  Pathways of viral antigen processing and presentation to CTL: defined by the mode of virus entry?

Authors:  E O Long; S Jacobson
Journal:  Immunol Today       Date:  1989-02

2.  Pseudorabies virus infections in explants of porcine nasal mucosa.

Authors:  J M Pol; W G Quint; G L Kok; J M Broekhuysen-Davies
Journal:  Res Vet Sci       Date:  1991-01       Impact factor: 2.534

3.  Multiple defects in the genome of pseudorabies virus can affect virulence without detectably affecting replication in cell culture.

Authors:  B Lomniczi; A S Kaplan; T Ben-Porat
Journal:  Virology       Date:  1987-11       Impact factor: 3.616

Review 4.  Antigen presentation pathways to class I and class II MHC-restricted T lymphocytes.

Authors:  T J Braciale; L A Morrison; M T Sweetser; J Sambrook; M J Gething; V L Braciale
Journal:  Immunol Rev       Date:  1987-08       Impact factor: 12.988

5.  Role of glycoprotein gIII of pseudorabies virus in virulence.

Authors:  T C Mettenleiter; C Schreurs; F Zuckermann; T Ben-Porat; A S Kaplan
Journal:  J Virol       Date:  1988-08       Impact factor: 5.103

6.  Envelope glycoprotein gp50 of pseudorabies virus is essential for virus entry but is not required for viral spread in mice.

Authors:  B Peeters; J Pol; A Gielkens; R Moormann
Journal:  J Virol       Date:  1993-01       Impact factor: 5.103

7.  A biological role for the major histocompatibility antigens.

Authors:  P C Doherty; R M Zinkernagel
Journal:  Lancet       Date:  1975-06-28       Impact factor: 79.321

8.  Immunohistologic study of pulmonary and lymphatic tissues from gnotobiotic pigs inoculated with ara-T-resistant strain of pseudorabies virus.

Authors:  M Narita; T Imada; M Haritani; H Kawamura
Journal:  Am J Vet Res       Date:  1989-11       Impact factor: 1.156

9.  Pseudorabies virus glycoproteins gII and gp50 are essential for virus penetration.

Authors:  I Rauh; T C Mettenleiter
Journal:  J Virol       Date:  1991-10       Impact factor: 5.103

10.  Pseudorabies virus envelope glycoproteins gp50 and gII are essential for virus penetration, but only gII is involved in membrane fusion.

Authors:  B Peeters; N de Wind; M Hooisma; F Wagenaar; A Gielkens; R Moormann
Journal:  J Virol       Date:  1992-02       Impact factor: 5.103

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