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双组分系统09对宿主传播过程中的代谢适应性和抗性很重要。

The Two-Component System 09 of Is Important for Metabolic Fitness and Resistance during Dissemination in the Host.

作者信息

Hirschmann Stephanie, Gómez-Mejia Alejandro, Kohler Thomas P, Voß Franziska, Rohde Manfred, Brendel Max, Hammerschmidt Sven

机构信息

Center for Functional Genomics of Microbes, Department of Molecular Genetics and Infection Biology, Interfaculty Institute for Genetics and Functional Genomics, University of Greifswald, 17487 Greifswald, Germany.

Central Facility for Microscopy, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.

出版信息

Microorganisms. 2021 Jun 23;9(7):1365. doi: 10.3390/microorganisms9071365.

Abstract

The two-component regulatory system 09 of has been shown to modulate resistance against oxidative stress as well as capsule expression. These data and the implication of TCS09 in cell wall integrity have been shown for serotype 2 strain D39. Other data have suggested strain-specific regulatory effects of TCS09. Contradictory data are known on the impact of TCS09 on virulence, but all have been explored using only the -mutant. In this study, we have therefore deleted one or both components of the TCS09 (SP_0661 and SP_0662) in serotype 4 TIGR4. In vitro growth assays in chemically defined medium (CDM) using sucrose or lactose as a carbon source indicated a delayed growth of nonencapsulated -mutants, while encapsulated wild-type TIGR4 and -mutants have reduced growth in CDM with glucose. Using a set of antigen-specific antibodies, immunoblot analysis showed that only the pilus 1 backbone protein RrgB is significantly reduced in TIGR4ΔΔ. Electron microscopy, adherence and phagocytosis assays showed no impact of TCS09 on the TIGR4 cell morphology and interaction with host cells. In contrast, in vivo infections and in particular competitive co-infection experiments demonstrated that TCS09 enhances robustness during dissemination in the host by maintaining bacterial fitness.

摘要

双组分调控系统09已被证明可调节对氧化应激的抗性以及荚膜表达。这些数据以及TCS09在细胞壁完整性方面的作用已在2型菌株D39中得到证实。其他数据表明TCS09具有菌株特异性调控作用。关于TCS09对毒力的影响存在相互矛盾的数据,但所有这些研究都仅使用了 -突变体进行探索。因此,在本研究中,我们在4型TIGR4中删除了TCS09的一个或两个组分(SP_0661和SP_0662)。在以蔗糖或乳糖作为碳源的化学限定培养基(CDM)中进行的体外生长试验表明,无荚膜的 -突变体生长延迟,而有荚膜的野生型TIGR4和 -突变体在以葡萄糖为碳源的CDM中生长受到抑制。使用一组抗原特异性抗体进行的免疫印迹分析表明,只有菌毛1主链蛋白RrgB在TIGR4ΔΔ中显著减少。电子显微镜、黏附及吞噬试验表明,TCS09对TIGR4的细胞形态以及与宿主细胞的相互作用没有影响。相比之下,体内感染尤其是竞争性共感染实验表明,TCS09通过维持细菌适应性增强了在宿主体内传播过程中的稳健性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d8f/8306541/e90cc99d2964/microorganisms-09-01365-g001.jpg

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