Simple Summary Fishmeal is an important but costly and limited protein ingredient in shrimp feed. Clostridium autoethanogenum protein is a promising alternative, yet high-level inclusion levels may adversely affect shrimp growth and health. This study evaluated whether dietary curcumin supplementation in Penaeus vannamei fed a diet in which 50% of the fishmeal was replaced with CAP. Three experimental groups were designed in this study: a fishmeal control, a high-CAP diet, and the same high-CAP diet supplemented with curcumin. After eight weeks, shrimp fed the high-CAP diet showed reduced growth, adverse histological changes in the intestine and hepatopancreas, lower nonspecific immune enzyme activities, and alterations in intestinal microbial community composition. Compared with the high-CAP group, curcumin supplementation was associated with improvements in growth performance, tissue morphology, immune enzyme activities, and intestinal microbial profiles. Transcriptomic analysis suggested that identified changes were associated with metabolic and immune-related biological processes. Because a fishmeal-based diet supplemented with curcumin was not included, these findings should be interpreted specifically under high-CAP dietary conditions. Overall, the results support the potential application of curcumin as a functional feed additive in CAP-based, low-fishmeal diets for shrimp.
Bacterial toxin-antitoxin (TA) systems are widespread genetic modules that regulate bacterial stress adaptation and pathogenicity. The atypical Type II psyrTA system encodes the toxin PsyrT with conserved RecQ-containing DEXDc and HELICc helicase domains, a rare architecture among characterized TA toxins. The toxic and pathogenic regulatory functions of helicase-containing TA toxins remain experimentally unvalidated. Here, we functionally characterized the psyrTA system in Pseudomonas plecoglossicida PQLYC4, the pathogen causing visceral white spot disease in large yellow croaker. Heterologous expression in Escherichia coli verified that PsyrT exerts potent growth-inhibitory toxicity, which is efficiently alleviated by cognate PsyrA via direct physical interaction. Deletion of psyrT markedly impaired biofilm formation, downregulated virulence gene transcription, reduced splenic colonization, and alleviated splenic histopathological damage in infected fish. Additionally, ΔpsyrT infection significantly attenuated host splenic cytokine transcriptional responses. Collectively, this study identifies PsyrT as a novel RecQ helicase domain-containing TA toxin and an important virulence modulator in P. plecoglossicida, expanding the functional diversity of bacterial TA systems.
Yudong Zheng, Jia-Tong Chen, Yan Teng et al.· Fish and Shellfish Immunolog...· 0 citations
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