In vitro and in vivo characterization of glycoprotein C-deleted infectious laryngotracheitis virus

J Gen Virol. 2010 Apr;91(Pt 4):847-57. doi: 10.1099/vir.0.016634-0. Epub 2009 Nov 25.

Abstract

Infectious laryngotracheitis is an important respiratory disease of chickens that is caused by an alphaherpesvirus [infectious laryngotracheitis virus (ILTV); Gallid herpesvirus 1]. As herpesvirus envelope glycoproteins are main targets of the humoral host immune response, they are of particular interest for development of vaccines, as well as of diagnostic tools. The conserved, N-glycosylated envelope protein gC has been identified as a major surface antigen of ILTV. To study the function of gC, we now isolated a gC-deleted ILTV recombinant as well as a gC rescuant after co-transfection of permissive chicken cells with virion DNA and transfer plasmids containing engineered subgenomic fragments. Like other alphaherpesvirus homologues, ILTV gC proved to be non-essential for replication. ILTV-DeltagC exhibited delayed penetration kinetics and slightly reduced plaque sizes in cultured chicken cells, whereas virus titres were not reduced significantly compared with wild-type or gC-rescued virus. In vivo studies revealed that ILTV-DeltagC is attenuated in chickens. However, infection with high doses of ILTV-DeltagC was still fatal for approximately 20 % of the animals, whereas wild-type or gC-rescued ILTV led to 50 % mortality. Interestingly, innate and specific immune responses against ILTV-DeltagC were not reduced but enhanced, and surviving chickens were protected completely against challenge infection. Furthermore, ILTV-DeltagC might serve as a basis for marker vaccines permitting differentiation between vaccinated and field-virus-infected animals, as gC-specific antibodies could be detected easily in sera of animals infected with wild-type ILTV.

MeSH terms

  • Animals
  • Chickens
  • Genome, Viral
  • Herpesvirus 1, Gallid / genetics
  • Herpesvirus 1, Gallid / immunology
  • Herpesvirus 1, Gallid / pathogenicity
  • Herpesvirus 1, Gallid / physiology*
  • Viral Envelope Proteins / immunology
  • Viral Envelope Proteins / physiology*
  • Virulence
  • Virus Internalization
  • Virus Replication

Substances

  • Viral Envelope Proteins