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低盐度激活海洋广宿主病原菌亚种的毒力程序。

Low salinity activates a virulence program in the generalist marine pathogen subsp. .

机构信息

Departamento de Microbioloxía e Parasitoloxía, Instituto de Acuicultura, Universidade de Santiago de Compostela , Santiago de Compostela, Spain.

Fish Immunology and Vaccinology Group, IBMC-Instituto de Biologia Molecular e Celular, Universidade do Porto , Porto, Portugal.

出版信息

mSystems. 2023 Jun 29;8(3):e0125322. doi: 10.1128/msystems.01253-22. Epub 2023 Jun 8.

Abstract

Facultative marine bacterial pathogens sense environmental signals so that the expression of virulence factors is upregulated on entry into hosts and downregulated during the free-living lifestyle in the environment. In this study, we utilized transcriptome sequencing to compare the transcriptional profiles of subsp. , a generalist pathogen that causes disease in diverse marine animals and fatal infections in humans at NaCl concentrations that mimic the free-living lifestyle or host internal milieu, respectively. We here show that NaCl concentration constitutes a major regulatory signal that shapes the transcriptome and uncover 1,808 differentially expressed genes (888 upregulated and 920 downregulated in response to low-salt conditions). Growth at 3% NaCl, a salinity that mimics the free-living lifestyle, upregulated genes involved in energy production, nitrogen metabolism, transport of compatible solutes, utilization of trehalose and fructose, and carbohydrate and amino acid metabolism with strong upregulation of the arginine deiminase system (ADS). In addition, we observed a marked increase in resistance to antibiotics at 3% NaCl. On the contrary, the low salinity conditions (1% NaCl) that mimic those encountered in the host triggered a virulence gene expression profile that maximized the production of the type 2 secretion system (T2SS)-dependent cytotoxins damselysin, phobalysin P, and a putative PirAB-like toxin, observations that were corroborated by the analysis of the secretome. Low salinity also upregulated the expression of iron-acquisition systems, efflux pumps, and other functions related to stress response and virulence. The results of this study greatly expand our knowledge of the salinity-responsive adaptations of a generalist and versatile marine pathogen. IMPORTANCE Pathogenic species experience continuous shifts of NaCl concentration in their life cycles. However, the impact of salinity changes in gene regulation has been studied in a small number of species. In this study, we analyzed the transcriptional response of subsp. (), a generalist and facultative pathogen, to changes in salinity, and demonstrate that growth at 1% NaCl in comparison to 3% NaCl triggers a virulence program of gene expression, with a major impact in the T2SS-dependent secretome. The decrease in NaCl concentration encountered by bacteria on entry into a host is proposed to constitute a regulatory signal that upregulates a genetic program involved in host invasion and tissue damage, nutrient scavenging (notably iron), and stress responses. This study will surely inspire new research on pathobiology, as well as on other important pathogens of the family and related taxa whose salinity regulons still await investigation.

摘要

兼性海洋细菌病原体感知环境信号,以便在进入宿主时上调毒力因子的表达,并在环境中的自由生活方式期间下调表达。在这项研究中,我们利用转录组测序来比较亚种的转录谱,这是一种普遍的病原体,可导致多种海洋动物患病,并在人类中引起致命感染,分别在模拟自由生活方式或宿主内部环境的 NaCl 浓度下。我们在这里表明,NaCl 浓度是塑造转录组的主要调节信号,并揭示了 1808 个差异表达基因(低盐条件下 888 个上调和 920 个下调)。在 3%NaCl 下生长,模拟自由生活方式的盐度,上调参与能量产生、氮代谢、相容溶质运输、海藻糖和果糖利用以及碳水化合物和氨基酸代谢的基因,精氨酸脱亚氨酶系统 (ADS) 强烈上调。此外,我们观察到在 3%NaCl 下抗生素抗性显着增加。相反,模拟宿主中遇到的低盐条件(1%NaCl)触发了一种毒力基因表达谱,最大限度地产生了依赖 II 型分泌系统 (T2SS) 的细胞毒素 damselysin、phobalysin P 和一种假定的 PirAB 样毒素,这一观察结果得到了对分泌组分析的证实。低盐还上调了铁摄取系统、外排泵和其他与应激反应和毒力相关的功能的表达。这项研究极大地扩展了我们对普遍存在和多功能海洋病原体盐度反应适应的知识。重要性 种在其生命周期中经历 NaCl 浓度的持续变化。然而,在基因调控方面,盐度变化的影响仅在少数 物种中进行了研究。在这项研究中,我们分析了兼性病原体亚种()对盐度变化的转录反应,并证明与 3%NaCl 相比,在 1%NaCl 下生长会引发依赖 T2SS 的外分泌体中基因表达的毒力程序,对 T2SS 的依赖外分泌体有重大影响。细菌进入宿主时遇到的 NaCl 浓度降低被提议构成调节信号,上调参与宿主入侵和组织损伤、营养物质掠夺(特别是铁)和应激反应的遗传程序。这项研究肯定会激发有关 病理学以及其他家族和相关分类群的重要病原体的新研究,这些病原体的盐度调节子仍有待研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce8e/10308900/953a93736222/msystems.01253-22.f001.jpg

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