Antibody and Cytokine Responses of Koalas (Phascolarctos cinereus) Vaccinated with Recombinant Chlamydial Major Outer Membrane Protein (MOMP) with Two Different Adjuvants

PLoS One. 2016 May 24;11(5):e0156094. doi: 10.1371/journal.pone.0156094. eCollection 2016.

Abstract

Developing a vaccine against Chlamydia is key to combating widespread mortalities and morbidities associated with this infection in koalas (Phascolarctos cinereus). In previous studies, we have shown that two or three doses of a Recombinant Major Outer Membrane Protein (rMOMP) antigen-based vaccine, combined with immune stimulating complex (ISC) adjuvant, results in strong cellular and humoral immune responses in koalas. We have also separately evaluated a single dose vaccine, utilising a tri-adjuvant formula that comprises polyphosphazine based poly I: C and host defense peptides, with the same antigen. This formulation also produced strong cellular and humoral immune responses in captive koalas. In this current study, we directly compared the host immune responses of two sub-groups of wild Chlamydia negative koalas in one population vaccinated with the rMOMP protein antigen and adjuvanted with either the ISC or tri-adjuvant formula. Overall, both adjuvants produced strong Chlamydia-specific cellular (IFN-γ and IL-17A) responses in circulating PBMCs as well as MOMP-specific and functional, in vitro neutralising antibodies. While the immune responses were similar, there were adjuvant-specific immune differences between the two adjuvants, particularly in relation to the specificity of the MOMP epitope antibody responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Pharmaceutic
  • Animals
  • Antibodies, Neutralizing / metabolism
  • Bacterial Outer Membrane Proteins / administration & dosage*
  • Bacterial Outer Membrane Proteins / immunology
  • Bacterial Vaccines / administration & dosage*
  • Bacterial Vaccines / immunology
  • Chlamydia Infections / immunology
  • Chlamydia Infections / prevention & control*
  • Immunity, Humoral
  • Interferon-gamma / metabolism
  • Interleukin-17 / metabolism
  • Phascolarctidae / immunology*
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / immunology
  • Vaccines, Synthetic / administration & dosage*
  • Vaccines, Synthetic / immunology

Substances

  • Adjuvants, Pharmaceutic
  • Antibodies, Neutralizing
  • Bacterial Outer Membrane Proteins
  • Bacterial Vaccines
  • Interleukin-17
  • Recombinant Proteins
  • Vaccines, Synthetic
  • Interferon-gamma

Grants and funding

This project was financially supported by an Australian Research Council (ARC) Linkage grant (LP1202000051) awarded to PT, A. Polkinghorne and KB. The funding organization did not play any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript and only provided financial support in the form of authors' salaries and research materials. This work was significantly supported by the Moreton Bay Rail Link project team and the Department of Transport and Main Roads, Queensland Government. These groups provided support for the overall field work and sampling of the koalas. JH and JL are employed by Endeavour Veterinary Ecology Pty Ltd and were responsible for field work with the koalas and for collecting the samples for analysis. Special thanks to the authors’ other collaborators including Queensland Department of Environment and Heritage Protection, Moreton Bay Regional Council, Endeavour Veterinary Ecology Pty Ltd, Australia Zoo Wildlife Hospital, Friends of the Koala, Lone Pine Koala Sanctuary and VIDO, Canada for their continued support of the authors’ broader project to develop a chlamydial vaccine for the koala.