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糖元代谢在毒力中的作用。

Role of glycogen metabolism in virulence.

机构信息

Division of biology, Kansas State University, Manhattan, Kansas, USA.

Department of Biology, Texas A&M University, College Station, Texas, USA.

出版信息

mSphere. 2024 Sep 25;9(9):e0031024. doi: 10.1128/msphere.00310-24. Epub 2024 Aug 27.

DOI:10.1128/msphere.00310-24
PMID:39189778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11423593/
Abstract

Glycogen plays a vital role as an energy reserve in various bacterial and fungal species. possesses a glycogen metabolism operon that contains genes for both glycogen synthesis and utilization. In our investigation, we focused on understanding the significance of glycogen metabolism in the physiology and pathogenesis of . To explore this, we engineered a JIR8094 strain lacking glycogen synthesis capability by introducing a group II intron into the gene, the operon's first component. Quantification of intracellular glycogen levels validated the impact of this modification. Interestingly, the mutant strain exhibited a 1.5-fold increase in toxin production compared with the parental strain, without significant changes in the sporulation rate. Our analysis also revealed that wild-type spores contained glycogen, whereas spores from the mutant strain lacking stored glycogen showed increased sensitivity to physical and chemical treatments and had a shorter storage life. By suppressing expression, the gene coding for glycogen-phosphorylase, via CRISPRi, we demonstrated that glycogen accumulation but not the utilization is needed for spore resilience in . Transmission electron microscopy analysis revealed a significantly lower core/cortex ratio in mutant strain spores. In hamster challenge experiments, both the parental and mutant strains colonized hosts similarly; however, the mutant strain failed to induce infection relapse after antibiotic treatment cessation. These findings highlight the importance of glycogen metabolism in spore resilience and suggest its role in disease relapse.IMPORTANCEThis study on the role of glycogen metabolism in highlights its critical involvement in the pathogen's energy management, its pathogenicity, and its resilience. Our results also revealed that glycogen presence in spores is pivotal for their structural integrity and resistance to adverse conditions, which is essential for their longevity and infectivity. Importantly, the inability of the mutant strain to cause infection relapse in hamsters post-antibiotic treatment pinpoints a potential target for therapeutic interventions, highlighting the importance of glycogen in disease dynamics. This research thus significantly advances our understanding of physiology and pathogenesis, offering new avenues for combating its persistence and recurrence.

摘要

糖原在各种细菌和真菌物种中作为能量储备起着至关重要的作用。 拥有一个糖原代谢操纵子,其中包含糖原合成和利用的基因。在我们的研究中,我们专注于了解糖原代谢在 的生理学和发病机制中的重要性。为了探索这一点,我们通过在 基因(操纵子的第一个元件)中引入一个 II 类内含子,构建了一个缺乏糖原合成能力的 JIR8094 突变菌株。通过定量细胞内糖原水平,验证了这种修饰的影响。有趣的是,与亲本菌株相比,突变菌株的毒素产量增加了 1.5 倍,而产孢率没有显著变化。我们的分析还表明,野生型 孢子含有糖原,而缺乏储存糖原的突变菌株的孢子对物理和化学处理更敏感,储存寿命更短。通过 CRISPRi 抑制 基因(编码糖原磷酸化酶)的表达,我们证明了在 中,糖原的积累而不是利用对于孢子的恢复力是必要的。透射电子显微镜分析显示, 突变菌株孢子的核心/皮质比显著降低。在仓鼠挑战实验中,亲本菌株和 突变菌株都能在宿主中定植;然而,突变菌株在停止抗生素治疗后未能引起感染复发。这些发现强调了糖原代谢在 孢子恢复力中的重要性,并表明其在疾病复发中的作用。

重要性

本研究强调了糖原代谢在 中的作用,突出了其在病原体能量管理、致病性和恢复力方面的关键作用。我们的研究结果还表明,孢子中糖原的存在对于其结构完整性和对不利条件的抗性至关重要,这对于其寿命和感染力至关重要。重要的是,突变菌株在抗生素治疗后不能引起仓鼠感染复发,这为治疗干预提供了一个潜在的靶点,突出了糖原在疾病动态中的重要性。因此,这项研究极大地推进了我们对 的生理学和发病机制的理解,为对抗其持久性和复发提供了新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/1a76280da5c9/msphere.00310-24.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/8252bddab400/msphere.00310-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/aa108421bc19/msphere.00310-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/97a8c4defee2/msphere.00310-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/190bda04b799/msphere.00310-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/54af6b888147/msphere.00310-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/2db446267c35/msphere.00310-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/1a76280da5c9/msphere.00310-24.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/8252bddab400/msphere.00310-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/aa108421bc19/msphere.00310-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/97a8c4defee2/msphere.00310-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/190bda04b799/msphere.00310-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/54af6b888147/msphere.00310-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/2db446267c35/msphere.00310-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bc6/11423593/1a76280da5c9/msphere.00310-24.f007.jpg

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