Identification of a potential antigen stimulating immune response against Vibrio parahaemolyticus infection in hybrid tilapia (Oreochromis aureus♂ × Oreochromis niloticus♀)

J Fish Dis. 2024 Mar;47(3):e13904. doi: 10.1111/jfd.13904. Epub 2023 Dec 8.

Abstract

Vibrio parahaemolyticus (V. parahaemolyticus) is a major pathogen that causes substantial losses in the marine fishery. With the emergence of antibiotic resistance, vaccines have become the most effective approach against V. parahaemolyticus infection. Adhesion factors on the cell surface are pivotal in the colonization and pathogenesis of V. parahaemolyticus within the host, highlighting their potential as vaccine candidates. This study aims to assess the immunogenicity and potential of recombinant V. parahaemolyticus MAM7 (rMAM7) as a vaccine candidate. Initially, we cloned and purified the MAM7 protein of V. parahaemolyticus. Moreover, after 4 weeks of vaccination, the fish were challenged with V. parahaemolyticus. rMAM7 demonstrated a certain protective effect. Immunological analysis revealed that rMAM7 immunization-induced antibody production and significantly increased acid phosphatase (ACP) and alkaline phosphatase (AKP) activity in hybrid tilapia. Furthermore, serum bactericidal tests demonstrated a lower bacterial survival rate in the rMAM7 group compared to PBS and rTrxa. qRT-PCR results indicated that rMAM7 significantly upregulated CD4, CD8 and IgM gene expression, suggesting the induction of Th1 and Th2 responses in hybrid tilapia. Overall, these findings highlight the potential application of MAM7 from V. parahaemolyticus in the development of protein vaccines.

Keywords: MAM7; Vibrio parahaemolyticus; antigen; hybrid tilapia; protein vaccine.

MeSH terms

  • Animals
  • Cichlids*
  • Fish Diseases* / microbiology
  • Immunity
  • Tilapia* / microbiology
  • Vaccines*
  • Vibrio Infections* / prevention & control
  • Vibrio Infections* / veterinary
  • Vibrio parahaemolyticus* / physiology

Substances

  • Vaccines

Associated data

  • RefSeq/BA000031.2