Immunogenicity of Outer Membrane Proteins VirB9-1 and VirB9-2, a Novel Nanovaccine against Anaplasma marginale

PLoS One. 2016 Apr 26;11(4):e0154295. doi: 10.1371/journal.pone.0154295. eCollection 2016.

Abstract

Anaplasma marginale is the most prevalent tick-borne livestock pathogen and poses a significant threat to cattle industry. In contrast to currently available live blood-derived vaccines against A. marginale, alternative safer and better-defined subunit vaccines will be of great significance. Two proteins (VirB9-1 and VirB9-2) from the Type IV secretion system of A. marginale have been shown to induce humoral and cellular immunity. In this study, Escherichia coli were used to express VirB9-1 and VirB9-2 proteins. Silica vesicles having a thin wall of 6 nm and pore size of 5.8 nm were used as the carrier and adjuvant to deliver these two antigens both as individual or mixed nano-formulations. High loading capacity was achieved for both proteins, and the mouse immunisation trial with individual as well as mixed nano-formulations showed high levels of antibody titres over 107 and strong T-cell responses. The mixed nano-formulation also stimulated high-level recall responses in bovine T-cell proliferation assays. These results open a promising path towards the development of efficient A. marginale vaccines and provide better understanding on the role of silica vesicles to deliver multivalent vaccines as mixed nano-formulations able to activate both B-cell and T-cell immunity, for improved animal health.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaplasma marginale / drug effects*
  • Anaplasma marginale / immunology
  • Anaplasmosis / immunology
  • Anaplasmosis / microbiology
  • Anaplasmosis / prevention & control*
  • Animals
  • Antibodies, Bacterial / biosynthesis*
  • Antigens, Bacterial / administration & dosage
  • Antigens, Bacterial / genetics
  • Antigens, Bacterial / immunology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology
  • B-Lymphocytes / pathology
  • Bacterial Outer Membrane Proteins / administration & dosage
  • Bacterial Outer Membrane Proteins / genetics
  • Bacterial Outer Membrane Proteins / immunology*
  • Bacterial Vaccines / administration & dosage
  • Bacterial Vaccines / genetics
  • Bacterial Vaccines / immunology
  • Cattle
  • Cattle Diseases / immunology
  • Cattle Diseases / microbiology
  • Cattle Diseases / prevention & control*
  • Cell Proliferation / drug effects
  • Cloning, Molecular
  • Drug Carriers / chemistry
  • Drug Carriers / metabolism
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Female
  • Gene Expression
  • Immunity, Cellular / drug effects*
  • Immunity, Humoral / drug effects*
  • Immunization
  • Lymphocyte Activation / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Nanoparticles / chemistry
  • Nanoparticles / ultrastructure
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Silicon Dioxide / administration & dosage
  • Silicon Dioxide / chemistry
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • T-Lymphocytes / pathology
  • Type IV Secretion Systems / genetics
  • Type IV Secretion Systems / metabolism

Substances

  • Antibodies, Bacterial
  • Antigens, Bacterial
  • Bacterial Outer Membrane Proteins
  • Bacterial Vaccines
  • Drug Carriers
  • Recombinant Proteins
  • Type IV Secretion Systems
  • Silicon Dioxide

Grants and funding

This work was supported by the Queensland Government Research Partnerships grant (Project 013936_471), https://www.business.qld.gov.au/industry/science/grants. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.