Determination of the minimum protective dose of a glycoprotein-G-deficient infectious laryngotracheitis virus vaccine delivered via eye-drop to week-old chickens

PLoS One. 2018 Dec 6;13(12):e0207611. doi: 10.1371/journal.pone.0207611. eCollection 2018.

Abstract

Infectious laryngotracheitis (ILT) is an upper respiratory tract disease of chickens that is caused by infectious laryngotracheitis virus (ILTV), an alphaherpesvirus. This disease causes significant economic loses in poultry industries worldwide. Despite widespread use of commercial live attenuated vaccines, many poultry industries continue to experience outbreaks of disease caused by ILTV. Efforts to improve the control of this disease have resulted in the generation of new vaccine candidates, including ILTV mutants deficient in virulence factors. A glycoprotein G deletion mutant vaccine strain of ILTV (ΔgG ILTV), recently licenced as Vaxsafe ILT (Bioproperties Pty Ltd), has been extensively characterised in vitro and in vivo, but the minimum effective dose required to protect inoculated animals has not been determined. This study performed a vaccination and challenge experiment to determine the minimum dose of ΔgG ILTV that, when delivered by eye-drop to seven-day-old specific pathogen-free chickens, would protect the birds from a robust challenge with a virulent field strain of virus (class 9 ILTV). A dose of 10(3.8) plaque forming units was the lowest dose capable of providing a high level of protection against challenge, as measured by clinical signs of disease, tracheal pathology and virus replication after challenge. This study has shown that the ΔgG ILTV vaccine strain is capable of inducing a high level of protection against a virulent field virus at a commercially feasible dose. These results lay the foundations upon which a commercial vaccine can be developed, thereby offering the potential to provide producers with another important tool to help control ILTV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chickens / immunology
  • Glycoproteins / pharmacology
  • Herpesvirus 1, Gallid / pathogenicity*
  • Ophthalmic Solutions / administration & dosage
  • Poultry Diseases / prevention & control
  • Vaccination / methods*
  • Vaccines / administration & dosage
  • Vaccines, Attenuated / pharmacokinetics*
  • Vaccines, Attenuated / pharmacology*
  • Viral Envelope Proteins / immunology
  • Viral Vaccines / pharmacokinetics
  • Viral Vaccines / pharmacology
  • Virulence Factors
  • Virus Replication

Substances

  • Glycoproteins
  • Ophthalmic Solutions
  • Vaccines
  • Vaccines, Attenuated
  • Viral Envelope Proteins
  • Viral Vaccines
  • Virulence Factors

Grants and funding

This work was funded by the Poultry Cooperative Research Centre through Sub-Project 1.1.10 awarded to project leader Joanne M Devlin and was funded by the Asia Pacific Centre for Animal Health. Mesula G. Korsa was supported by Australian Government Research Training Program (RTP) scholarship. There was no additional external funding received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.