Interleukine-1β (IL-1β) is the first identified pro-inflammatory cytokine, which is cleaved by caspase-1 following the inflammasomes activation, playing critical roles in innate immunity. However, few studies have been performed to characterize the IL-1β in lower vertebrates. Herein, we distinguished the Scophthalmus maximus IL-1β (SmIL-1β) from three IL-1β like sequences and found that SmIL-1β was cleaved by S. maximus caspase at a non-conserved Asp86, then targeted to the plasma membrane. Moreover, during the immersion infection of Edwardsiella piscicida, we found that E. piscicida were mainly colonized in gills at early time points and invaded to systemic sites after 5 days post infection, which was consistent with the dynamic up-regulated transcription of SmIL-1β. Furthermore, knockdown of SmIL-1β promotes the bacterial colonization in gills at early time points and result into systemic colonization, while overexpression of SmIL-1β hampers the bacterial colonization in both spleen and kidney. Taken together, these data provide new insights into the molecular mechanisms of SmIL-1β and reveal its role in limiting bacterial infection in vivo, which will support the idea for better understanding the evolutionary of IL-1β functions in teleost.,Copyright © 2019 Elsevier Ltd. All rights reserved.