Cargando…

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

Uncovering the mechanism underlying the pathogenesis of Edwardsiella piscicida-induced enteritis is essential for global aquaculture. In the present study, we identified E. piscicida as a lethal pathogen of the big-belly seahorse (Hippocampus abdominalis) and revealed its pathogenic pattern and char...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lele, Wang, Fang, Jia, Longwu, Yan, Hansheng, Gao, Longkun, Tian, Yanan, Su, Xiaolei, Zhang, Xu, Lv, Chunhui, Ma, Zhenhao, Xue, Yuanyuan, Lin, Qiang, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193291/
https://www.ncbi.nlm.nih.gov/pubmed/37215132
http://dx.doi.org/10.3389/fimmu.2023.1135588
_version_ 1785043804431056896
author Zhang, Lele
Wang, Fang
Jia, Longwu
Yan, Hansheng
Gao, Longkun
Tian, Yanan
Su, Xiaolei
Zhang, Xu
Lv, Chunhui
Ma, Zhenhao
Xue, Yuanyuan
Lin, Qiang
Wang, Kai
author_facet Zhang, Lele
Wang, Fang
Jia, Longwu
Yan, Hansheng
Gao, Longkun
Tian, Yanan
Su, Xiaolei
Zhang, Xu
Lv, Chunhui
Ma, Zhenhao
Xue, Yuanyuan
Lin, Qiang
Wang, Kai
author_sort Zhang, Lele
collection PubMed
description Uncovering the mechanism underlying the pathogenesis of Edwardsiella piscicida-induced enteritis is essential for global aquaculture. In the present study, we identified E. piscicida as a lethal pathogen of the big-belly seahorse (Hippocampus abdominalis) 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 (P < 0.01) to promote pathogen motility, adherence, and invasion. Legiobactin, IraAB, and Hpt could increase ABC transporter activity (P < 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 (P < 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 (P < 0.01) to release toxins and kill the host. Throughout the pathogenic process, BopD, PhoP, and BfmRS significantly activated the two-component system (P < 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 (P < 0.01), and they can be used for characterizing E. piscicida infection. Overall, the present study systematically revealed how a combination of virulence factors mediate E. piscicida-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.
format Online
Article
Text
id pubmed-10193291
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-101932912023-05-19 Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors Zhang, Lele Wang, Fang Jia, Longwu Yan, Hansheng Gao, Longkun Tian, Yanan Su, Xiaolei Zhang, Xu Lv, Chunhui Ma, Zhenhao Xue, Yuanyuan Lin, Qiang Wang, Kai Front Immunol Immunology Uncovering the mechanism underlying the pathogenesis of Edwardsiella piscicida-induced enteritis is essential for global aquaculture. In the present study, we identified E. piscicida as a lethal pathogen of the big-belly seahorse (Hippocampus abdominalis) 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 (P < 0.01) to promote pathogen motility, adherence, and invasion. Legiobactin, IraAB, and Hpt could increase ABC transporter activity (P < 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 (P < 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 (P < 0.01) to release toxins and kill the host. Throughout the pathogenic process, BopD, PhoP, and BfmRS significantly activated the two-component system (P < 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 (P < 0.01), and they can be used for characterizing E. piscicida infection. Overall, the present study systematically revealed how a combination of virulence factors mediate E. piscicida-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. Frontiers Media S.A. 2023-05-03 /pmc/articles/PMC10193291/ /pubmed/37215132 http://dx.doi.org/10.3389/fimmu.2023.1135588 Text en Copyright © 2023 Zhang, Wang, Jia, Yan, Gao, Tian, Su, Zhang, Lv, Ma, Xue, Lin and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Lele
Wang, Fang
Jia, Longwu
Yan, Hansheng
Gao, Longkun
Tian, Yanan
Su, Xiaolei
Zhang, Xu
Lv, Chunhui
Ma, Zhenhao
Xue, Yuanyuan
Lin, Qiang
Wang, Kai
Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title_full Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title_fullStr Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title_full_unstemmed Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title_short Edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
title_sort edwardsiella piscicida infection reshapes the intestinal microbiome and metabolome of big-belly seahorses: mechanistic insights of synergistic actions of virulence factors
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193291/
https://www.ncbi.nlm.nih.gov/pubmed/37215132
http://dx.doi.org/10.3389/fimmu.2023.1135588
work_keys_str_mv AT zhanglele edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT wangfang edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT jialongwu edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT yanhansheng edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT gaolongkun edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT tianyanan edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT suxiaolei edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT zhangxu edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT lvchunhui edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT mazhenhao edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT xueyuanyuan edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT linqiang edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors
AT wangkai edwardsiellapiscicidainfectionreshapestheintestinalmicrobiomeandmetabolomeofbigbellyseahorsesmechanisticinsightsofsynergisticactionsofvirulencefactors