AI Article Synopsis

  • The study evaluated the immune responses in mice inoculated with a genetically modified strain of Mycobacterium bovis BCG that expresses the MSP1a antigen from Anaplasma marginale.
  • The results showed significant seroconversion to MSP1a in mice, particularly with the rBCG/pUS2000 construct, which was 26 times higher than pre-immunization levels after 63 days and remained sustained for 6 months.
  • The research indicates that the level of antigen expression affects the immune response, highlighting the potential of using recombinant BCG in cattle to help control bovine anaplasmosis.

Article Abstract

Humoral and cellular immune responses of mice inoculated with recombinant Mycobacterium bovis BCG expressing the MSP1a antigen of Anaplasma marginale were evaluated. The msp1a gene was amplified by PCR and cloned into the mycobacterial expression vectors pUS2000 and pMIP12. Immunization of isogenic BALB/c mice with the rBCG/pUS2000-msp1a construct induced significant seroconversion to MSP1a (p<0.001), which was 26 times above pre-immunization levels at day 63 post-initial immunization and which remained stable for the duration of the experiment (6 months). In contrast, rBCG/pMIP12-msp1a induced seroconversion at a level of 6 times above pre-immunization values, which peaked at day 63. Western blot analysis showed that sera derived from mice vaccinated with either rBCG construct recognized both native and recombinant forms of A. marginale MSP1a. In contrast to the humoral response data, immunization with rBCG/pMIP12-msp1a was found to induce a markedly stronger cellular response than that recorded for BCG/pUS2000-msp1a. These observations clearly demonstrated the immunogenicity of recombinant BCG expressing the MSP1a antigen and suggested that the immune responses were influenced by the level of antigen expression. The results of this research warrant studies of recombinant M. bovis BCG expressing MSP1a in cattle to test for protective antibody production for control of bovine anaplasmosis.

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http://dx.doi.org/10.1016/j.vaccine.2006.05.028DOI Listing

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