Immune Responses Induced by Recombinant Bacillus Subtilis Expressing the Hemagglutinin Protein of H5N1 in chickens

Sci Rep. 2016 Dec 16:6:38403. doi: 10.1038/srep38403.

Abstract

To develop an effective, safe, and convenient vaccine for the prevention of highly pathogenic avian influenza (HPAI) H5N1, we have constructed a recombinant Bacillus subtilis strain (B.S.-HA) expressing the hemagglutinin (HA) protein. Then we evaluated the immune function in chicken bone marrow derived dendritic cells (BM-DCs), and the immune response after oral immunization. Our results show that the recombinant Bacillus subtilis B.S.-HA could be sampled by BM-DCs in vitro and increase the BM-DCs major histocompatibility complex (MHC) II phenotype. The weight, height of the small intestine villus, and lymphoid tissue area of the ileum increased significantly in B.S.-HA immunized chickens (P < 0.05 or P < 0.01). B.S.-HA induced the secretion of cytokines and the expression of Toll-like receptors in the trachea and small intestine (P < 0.05 or P < 0.01). In addition, B.S.-HA elevated the specific IgA titers in the trachea, IgG and HI antibody titers in serum (P < 0.05 or P < 0.01). Therefore, B.S.-HA provides a potential novel strategy and approach for developing an H5N1 vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Bacillus subtilis / physiology*
  • Body Weight / drug effects
  • Bone Marrow Cells / metabolism
  • Cells, Cultured
  • Chickens / immunology*
  • Chickens / microbiology*
  • Chickens / virology
  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Hemagglutinin Glycoproteins, Influenza Virus / metabolism*
  • Immunization
  • Influenza A Virus, H5N1 Subtype / physiology*
  • Interleukin-4 / pharmacology
  • Intestine, Small / drug effects
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism
  • Lymphoid Tissue / drug effects
  • Plasmids / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Recombination, Genetic / genetics*
  • Spleen / cytology
  • Toll-Like Receptors / metabolism

Substances

  • Hemagglutinin Glycoproteins, Influenza Virus
  • Recombinant Fusion Proteins
  • Toll-Like Receptors
  • Interleukin-4
  • Granulocyte-Macrophage Colony-Stimulating Factor