In Vitro and In Vivo Relevance of Infectious Laryngotracheitis Virus gJ Proteins That Are Expressed from Spliced and Nonspliced mRNAs
Open Access
- 15 January 2005
- journal article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 79 (2) , 705-716
- https://doi.org/10.1128/jvi.79.2.705-716.2005
Abstract
The positional homologue in the infectious laryngotracheitis virus (ILTV) genome of the glycoprotein gJ gene of herpes simplex virus and the gp2 gene of equine herpesvirus 1 is expressed into four proteins of 85, 115, 160, and 200 kDa (J. Veits, B. Köllner, J. P. Teifke, H. Granzow, T. C. Mettenleiter, and W. Fuchs, Avian Dis. 47: 330-342, 2003). RNA analyses revealed that these proteins are expressed from two different late (γ2) transcripts, an unspliced 5.5-kb and a spliced 4.3-kb mRNA that are translated into proteins of 985 and 611 amino acids, respectively. ILTV gJ is incorporated into virions and is modified by N- and O-linked glycosylation. After cotransfection of chicken cells with genomic DNA of a pathogenic ILTV strain and transfer plasmids, gJ-negative ILTV mutants could be isolated. In vitro growth studies demonstrated that deletion of the gJ gene has only minor effects on direct cell-to-cell spread as measured by plaque size. However, progeny virus titers of ILTV-ΔgJ were significantly reduced in comparison to those of the parental virus and a gJ rescue mutant. After experimental infection of chickens the gJ rescue mutant, like wild-type ILTV, caused severe disease and considerable mortality, whereas ILTV-ΔgJ was significantly attenuated. All immunized animals were protected against subsequent challenge infection with virulent ILTV. In sera collected after immunization with the gJ-rescue mutant or with wild-type ILTV, gJ-specific antibodies were detectable by immunofluorescence on cells that had been transfected with a gJ expression plasmid. As expected, no gJ-specific antibodies were found in sera obtained from chickens immunized with ILTV-ΔgJ. Thus, gJ deletion mutants of ILTV might be usable as attenuated live-virus vaccines. Furthermore, the gJ gene might constitute a reliable marker for serological discrimination between vaccinated and field virus-infected chickens.Keywords
This publication has 53 references indexed in Scilit:
- Five unique open reading frames of infectious laryngotracheitis virus are expressed during infection but are dispensable for virus replication in cell cultureJournal of General Virology, 2003
- Eradication of Aujeszky's Disease in GermanyJournal of Veterinary Medicine, Series B, 2003
- Nucleotide sequence of the left-terminus of infectious laryngotracheitis virus (Gallid herpesvirus 1) SA-2 strainArchiv für die gesamte Virusforschung, 1997
- Nucleotide sequence of infectious laryngotracheitis virus (gallid herpesvirus 1) ICP4 geneVirus Research, 1995
- Use of λgt11 and monoclonal antibodies to map the gene for the 60,000 dalton glycoprotein of infectious laryngotracheitis virusVirus Genes, 1993
- Gallid herpesvirus 1 (infectious laryngotracheitis virus): cloning and physical maps of the SA-2 strainArchiv für die gesamte Virusforschung, 1991
- Genome isomerism in two alphaherpesviruses:Herpesvirus saimiri-1(Herpesvirus tamarinus) and avian infectious laryngotracheitis virusArchiv für die gesamte Virusforschung, 1987
- The Complete DNA Sequence of Varicella-Zoster VirusJournal of General Virology, 1986
- Sequence determination and genetic content of the short unique region in the genome of herpes simplex virus type 1Journal of Molecular Biology, 1985
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970