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神经坏死病毒和哈维氏弧菌的共感染增加了点带石斑鱼(Epinephelus coioides)的死亡率,并加重了疾病的严重程度。

Co-infection of nervous necrosis virus and Vibrio harveyi increased mortality and worsened the disease severity in the orange-spotted grouper (Epinephelus coioides).

作者信息

Guan Lingfeng, Li Xinshuai, Chen Jinpeng, Wang Liqun, Zhang Xinyue, Sun Hongyan, Li Yanwei, Yang Min, Qin Qiwei, Wang Shaowen

机构信息

College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, PR China.

College of Marine Sciences, South China Agricultural University, Guangzhou, 510642, PR China; Nansha-South China Agricultural University Fishery Research Institute, Guangzhou, 511464, PR China.

出版信息

Fish Shellfish Immunol. 2025 Mar;158:110117. doi: 10.1016/j.fsi.2025.110117. Epub 2025 Jan 9.

Abstract

Co-infections of different pathogenic microorganisms usually cause complex effects, and receive more attention. Red-grouper nervous necrosis virus (RGNNV) and Vibrio are the common viral and bacterial pathogens of fish, and are often detected simultaneously in diseased fish. However, the understanding of co-infection of RGNNV and Vibrio is still unclear. In this study, we have established a grouper (Epinephelus coioides) model of the co-infection of RGNNV and Vibrio harveyi (V. harveyi). Compared with single pathogen infection, co-infection of RGNNV and V. harveyi significantly caused more severe pathologic changes with higher mortality (P < 0.05), and promoted the proliferation of the pathogens by RNA-FISH and qRT-PCR (P < 0.05), demonstrating a synergistic effect of RGNNV and V. harveyi in grouper. Furthermore, we found that V. harveyi inhibited the induction and migration of neutrophils by RGNNV, resulting the obviously reduced neutrophils of co-infection groups (P < 0.05). In addition, transcriptome analysis showed that differentially expressed genes (DEGs) of brain tissues of different experimental groups were enriched in immune signaling pathways, such as JAK-STAT signaling, NF-κB signaling and TNF signaling pathways. For the liver and spleen tissues, the DEGs of different experimental groups were enriched in metabolism-related pathways, such as glycolysis/gluconeogenesis and glycerolipid metabolism. Further analysis of the selected DEGs, co-infection of RGNNV and V. harveyi significantly suppressed the host immune response and up-regulated host glucose and lipid metabolism, compared with single-pathogen infection. Taken together, the RGNNV and V. harveyi make synergic reaction in grouper, possibly due to the down regulation of host immune response and up regulation of metabolism to facilitate the replication of both pathogens. These results provide new insights into the pathogenesis of multiple pathogens, and contribute to develop new therapies.

摘要

不同病原微生物的共感染通常会产生复杂的影响,因而受到更多关注。红斑石斑鱼神经坏死病毒(RGNNV)和弧菌是鱼类常见的病毒和细菌病原体,在患病鱼中经常同时被检测到。然而,对于RGNNV和弧菌共感染的了解仍不清楚。在本研究中,我们建立了石斑鱼(Epinephelus coioides)RGNNV和哈维氏弧菌(V. harveyi)共感染模型。与单一致病菌感染相比,RGNNV和哈维氏弧菌共感染显著导致更严重的病理变化和更高的死亡率(P < 0.05),并通过RNA-FISH和qRT-PCR促进了病原体的增殖(P < 0.05),证明了RGNNV和哈维氏弧菌在石斑鱼中的协同作用。此外,我们发现哈维氏弧菌抑制了RGNNV诱导的中性粒细胞迁移,导致共感染组中性粒细胞明显减少(P < 0.05)。此外,转录组分析表明,不同实验组脑组织的差异表达基因(DEGs)富集于免疫信号通路,如JAK-STAT信号通路、NF-κB信号通路和TNF信号通路。对于肝脏和脾脏组织,不同实验组的DEGs富集于代谢相关通路,如糖酵解/糖异生和甘油脂质代谢。与单一致病菌感染相比,对所选DEGs的进一步分析表明,RGNNV和哈维氏弧菌共感染显著抑制了宿主免疫反应,并上调了宿主的糖代谢和脂代谢。综上所述,RGNNV和哈维氏弧菌在石斑鱼中产生协同反应,可能是由于宿主免疫反应下调和代谢上调,以促进两种病原体的复制。这些结果为多种病原体的发病机制提供了新的见解,并有助于开发新的治疗方法。

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