- Poster presentation
- Open Access
Analyses reveal a novel avirulent Streptococcus suis Serotype 2 strain that induces protective immunity against challenge with the highly virulent strains
© Tang; licensee BioMed Central Ltd. 2010
- Published: 11 May 2010
- Tumor Necrosis Factor Alpha
- Protective Immunity
- Genome Rearrangement
- Pathogenic Strain
- Model Strain
By comparative analysis of the bacterial genomesm of Streptococcus suis serotype 2 both virulent and avirulent strains are instrumental in the development of vaccines and the functional characterization of important of genetic determinants.
We isolated from a clinically healthy pig an avirulent strain, 05HAS68.
By comparing the genomes of the virulent and avirulent strains, we observed massive genome rearrangements that may result in alterations in gene expression and, in turn, causing enormous single gene gain and loss for the S. suis 2 species. It is most interesting that both virulent and avirulent species feature a similarly structured genomic island (GEI) which carries different idiosyncratic systems as an adoptive evolutionary response. Strikingly, all of the animals vaccinated with the avirulent strain 05HAS68 were protected from challenge infection with the most virulent S. suis 2 strain, 05ZYH33, and, furthermore, the protective immunity could be transferred with T cells and plasma from the vaccinated pigs to unimmunized animals. Increased production of tumor necrosis factor alpha (TNF-alpha) and gamma interferon (IFN-gamma) in peripheral blood of the immunized animals may be attributed to the protective immunity elicited by the live vaccine.
Since the S. suis 2 strains command large genetic diversity, it is almost impossible to achieve global protection for all S. suis 2 pathogenic strains by depending on one, or even several, virulence-related substances as vaccines. In view of our results, both humoral and cellular immunities induced by live 05HAS68-based vaccine are required for the specific protection against virulent S. suis strains; therefore, we suggest reconsideration of research strategy in terms of model strains to test for vaccine design.
This article is published under license to BioMed Central Ltd.