在铁限制条件下,Tenacibaculum dicentrarchi 的蛋白质组特征显示,与铁氧化和还原代谢、铁吸收系统和滑行运动有关的蛋白质上调。

IF 2.2 3区 农林科学 Q2 FISHERIES Journal of fish diseases Pub Date : 2024-06-29 DOI:10.1111/jfd.13984
Ruben Avendaño-Herrera, Macarena Echeverría-Bugueño, Mauricio Hernández, Pablo Saldivia, Rute Irgang
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引用次数: 0

摘要

疫苗设计策略包括识别可能参与病原体-宿主相互作用的蛋白质。这项蛋白质组学研究的目的是确定铁限制如何影响双壳丝核菌(Tenacibaculum dicentrarchi)的蛋白质表达,主要关注毒力因子和与铁吸收相关的蛋白质。蛋白质组分析是在模拟宿主环境的正常(对照)和铁限制条件下生长的两株 T. dicentrarchi 菌株中进行的。我们的研究结果表明,双壳线虫的模式菌株 CECT 7612T 和智利菌株 TdCh05 表达的蛋白质存在差异。然而,二者对铁缺乏的反应是相同的,在铁限制条件下,与铁氧化和还原代谢(如 SufA、YpmQ、SufD)、苷元转运(如 ExbD、TonB 依赖性受体、HbpA)、血红素化合物生物合成和铁转运体相关的蛋白质表达量增加。两种菌株中参与滑行运动的蛋白质,如 GldL 和 SprE,也出现了上调。在铁限制条件下,代谢蛋白,尤其是与氨基酸生物合成相关的蛋白,出现了负向差异调控,这反映了铁供应对细菌代谢的影响。此外,与类型菌株相比,TdCh05 菌株表现出与滑行运动机制和噬菌体感染控制相关的独特蛋白质。这些蛋白质组已被确定为黄杆菌科(包括天牛属)中的毒力因子。这些结果建立在我们之前关于铁获取机制的报告基础之上,可为今后的研究奠定基础,旨在阐明所描述的一些蛋白质在tenacibaculosis感染过程中的作用,以及开发潜在的疫苗。
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Proteomic characterization of Tenacibaculum dicentrarchi under iron limitation reveals an upregulation of proteins related to iron oxidation and reduction metabolism, iron uptake systems and gliding motility

A strategy for vaccine design involves identifying proteins that could be involved in pathogen–host interactions. The aim of this proteomic study was to determine how iron limitation affects the protein expression of Tenacibaculum dicentrarchi, with a primary focus on virulence factors and proteins associated with iron uptake. The proteomic analysis was carried out using two strains of T. dicentrarchi grown under normal (control) and iron-limited conditions, mimicking the host environment. Our findings revealed differences in the proteins expressed by the type strain CECT 7612T and the Chilean strain TdCh05 of T. dicentrarchi. Nonetheless, both share a common response to iron deprivation, with an increased expression of proteins associated with iron oxidation and reduction metabolism (e.g., SufA, YpmQ, SufD), siderophore transport (e.g., ExbD, TonB-dependent receptor, HbpA), heme compound biosynthesis, and iron transporters under iron limitation. Proteins involved in gliding motility, such as GldL and SprE, were also upregulated in both strains. A negative differential regulation of metabolic proteins, particularly those associated with amino acid biosynthesis, was observed under iron limitation, reflecting the impact of iron availability on bacterial metabolism. Additionally, the TdCh05 strain exhibited unique proteins associated with gliding motility machinery and phage infection control compared to the type strain. These groups of proteins have been identified as virulence factors within the Flavobacteriaceae family, including the genus Tenacibaculum. These results build upon our previous report on iron acquisition mechanisms and could lay the groundwork for future studies aimed at elucidating the role of some of the described proteins in the infectious process of tenacibaculosis, as well as in the development of potential vaccines.

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来源期刊
Journal of fish diseases
Journal of fish diseases 农林科学-海洋与淡水生物学
CiteScore
4.60
自引率
12.00%
发文量
170
审稿时长
6 months
期刊介绍: Journal of Fish Diseases enjoys an international reputation as the medium for the exchange of information on original research into all aspects of disease in both wild and cultured fish and shellfish. Areas of interest regularly covered by the journal include: -host-pathogen relationships- studies of fish pathogens- pathophysiology- diagnostic methods- therapy- epidemiology- descriptions of new diseases
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