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Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors

Frontiers in Immunology 2023 15 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Xu Zhang, Lele Zhang, Yuanyuan Xue, Fang Wang, Yanan Tian, Longwu Jia, Longwu Jia, Yanan Tian, Hansheng Yan, Hansheng Yan, Longkun Gao, Longkun Gao, Yanan Tian, Xu Zhang, Xiaolei Su, Xu Zhang, Chunhui Lv, Chunhui Lv, Zhenhao Ma, Zhenhao Ma, Yuanyuan Xue, Yuanyuan Xue, Qiang Lin, Kai Wang

Summary

Researchers identified the bacterium Edwardsiella piscicida as a lethal pathogen in big-belly seahorses and mapped how its virulence factors reshape the intestinal microbiome and metabolism of infected animals. They found 15 core virulence factors that work together to disrupt gut bacteria, increase harmful metabolites, and trigger intestinal inflammation. The study provides insights into how bacterial infections exploit the gut environment, which could inform disease prevention strategies in aquaculture.

Body Systems

Uncovering the mechanism underlying the pathogenesis of <i>Edwardsiella piscicida-</i>induced enteritis is essential for global aquaculture. In the present study, we identified <i>E. piscicida</i> as a lethal pathogen of the big-belly seahorse (<i>Hippocampus abdominalis</i>) and revealed its pathogenic pattern and characteristics by updating our established bacterial enteritis model and evaluation system. Conjoint analysis of metagenomic and metabolomic data showed that 15 core virulence factors could mutually coordinate the remodeling of intestinal microorganisms and host metabolism and induce enteritis in the big-belly seahorse. Specifically, the Flagella, Type IV pili, and Lap could significantly increase the activities of the representative functional pathways of both flagella assembly and bacterial chemotaxis in the intestinal microbiota (<i>P</i> < 0.01) to promote pathogen motility, adherence, and invasion. Legiobactin, IraAB, and Hpt could increase ABC transporter activity (<i>P</i> < 0.01) to compete for host nutrition and promote self-replication. Capsule1, HP-NAP, and FarAB could help the pathogen to avoid phagocytosis. Upon entering epithelial cells and phagocytes, Bsa T3SS and Dot/Icm could significantly increase bacterial secretion system activity (<i>P</i> < 0.01) to promote the intracellular survival and replication of the pathogen and the subsequent invasion of the neighboring tissues. Finally, LPS3 could significantly increase lipopolysaccharide biosynthesis (<i>P</i> < 0.01) to release toxins and kill the host. Throughout the pathogenic process, BopD, PhoP, and BfmRS significantly activated the two-component system (<i>P</i> < 0.01) to coordinate with other VFs to promote deep invasion. In addition, the levels of seven key metabolic biomarkers, Taurine, L-Proline, Uridine, L-Glutamate, Glutathione, Xanthosine, and L-Malic acid, significantly decreased (<i>P</i> < 0.01), and they can be used for characterizing <i>E. piscicida</i> infection. Overall, the present study systematically revealed how a combination of virulence factors mediate <i>E. piscicida</i>-induced enteritis in fish for the first time, providing a theoretical reference for preventing and controlling this disease in the aquaculture of seahorses and other fishes.

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