Abstract:[Objective] As one of the key enzymes of the glycolysis in E. tarda, GAPDH was previously identified to be a broad-spectrum antigen and could be used as the target of bacterial vaccine design in aquaculture. We explore the mechanism of secretion of GAPDH in E. tarda. [Methods] Secretion of GAPDH in E. tarda EIB202 and mutants of several secretory pathways were analyzed by Western blot and ELISA. The levels of GAPDH in the supernatants of mutant library were analyzed through high-throughput screening. Quantitative real-time PCR was used to compare the mRNA expressions of mutants obtained from screening. [Results] Secretion of GAPDH in E. tarda is associated with classical secretion systems. Through high-throughput screening, two mutants ΔesrA and ΔesrC were found to have higher levels of GAPDH in the supernatants. Lacking of these two genes lead to significant up-regulation of secretion of GAPDH. [Conclusion] EsrA and EsrC both played a negative regulation role in GAPDH secretion.