Attenuated as a Vaccine Vector for the Delivery of OMPW, the Outer Membrane Protein of .

(LM) is a gram-positive facultative intracellular pathogen that could stimulate host to produce inflammatory response, cell-mediated immunity, and humoral immunity. In this study, an attenuated live vector vaccine for (AH) named was successfully constructed using an attenuated vector named , in which , , A, and B genes were deleted from wild-type LM. To construct , a recombinant plasmid pERL3-dat-ompW obtained by inserting the gene from and outer membrane protein gene W from AH into pERL3 plasmid was transformed into cell. The safety and immunogenicity of as an attenuated vector vaccine for delivery of OMPW were assessed through analyzing invasion to Caco-2 cells and mice, cytokine production of macrophagocyte and mouse splenocytes, and T-cell proliferation of mouse splenocytes. Serum titers against AH and the immunoprotective effect of the vaccine to mice were also measured after intravenous injection with vaccine for four times. The results showed that the live vector vaccine for AH exhibited high attenuation in invading Caco-2 cells and mice than did . Real-time PCR (RT-PCR) showed that cytokines (e.g., TNF-α, IL-6, and IL-1β from macrophages; and IL-6 and IFN-γ from mouse splenocytes) had significantly increased after immunization by . Meanwhile, the vaccine could induce the production of CD3CD4 and CD3CD8 T-cell proliferation of mice and generate effective immunoprotection against lethal challenge of 20 × LD AH. All these results indicated that the attenuated could be used as a live vector for the delivery of the exogenous gene, not only possessing safety but also providing high immunogenicity. The successful application in the AH vaccine further showed that it could be used in other fields such as vaccines in cancer or infectious diseases.