Ribosomal-processing cysteine protease homolog modulates Streptococcus mutans glucan production and interkingdom interactions.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY Journal of Bacteriology Pub Date : 2024-07-25 Epub Date: 2024-06-20 DOI:10.1128/jb.00104-24
Puthayalai Treerat, Camilla de Mattos, Molly Burnside, Hua Zhang, Yanting Zhu, Zhengzhong Zou, David Anderson, Hui Wu, Justin Merritt, Jens Kreth
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Abstract

Glucan-dependent biofilm formation is a crucial process in the establishment of Streptococcus mutans as a cariogenic oral microbe. The process of glucan formation has been investigated in great detail, with glycosyltransferases GtfB, GtfC, and GtfD shown to be indispensable for the synthesis of glucans from sucrose. Glucan production can be visualized during biofilm formation through fluorescent labeling, and its abundance, as well as the effect of glucans on general biofilm architecture, is a common phenotype to study S. mutans virulence regulation. Here, we describe an entirely new phenotype associated with glucan production, caused by a mutation in the open reading frame SMU_848, which is located in an operon encoding ribosome-associated proteins. This mutation led to the excess production and accumulation of glucan-containing droplets on the surface of biofilms formed on agar plates after prolonged incubation. While not characterized in S. mutans, SMU_848 shows homology to the phage-related ribosomal protease Prp, essential in cleaving off the N-terminal extension of ribosomal protein L27 for functional ribosome assembly in Staphylococcus aureus. We present a further characterization of SMU_848/Prp, demonstrating that the deletion of this gene leads to significant changes in S. mutans gtfBC expression. Surprisingly, it also profoundly impacts the interkingdom interaction between S. mutans and Candida albicans, a relevant dual-species interaction implicated in severe early childhood caries. The presented data support a potential broader role for SMU_848/Prp, possibly extending its functionality beyond the ribosomal network to influence important ecological processes.

Importance: Streptococcus mutans is an important member of the oral biofilm and is implicated in the initiation of caries. One of the main virulence mechanisms is the glucan-dependent formation of biofilms. We identified a new player in the regulation of glucan production, SMU_848, which is part of an operon that also encodes for ribosomal proteins L27 and L21. A mutation in SMU_848, which encodes a phage-related ribosomal protease Prp, leads to a significant accumulation of glucan-containing droplets on S. mutans biofilms, a previously unknown phenotype. Further investigations expanded our knowledge about the role of SMU_848 beyond its role in glucan production, including significant involvement in interkingdom interactions, thus potentially playing a global role in the virulence regulation of S. mutans.

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核糖体处理半胱氨酸蛋白酶同源物调节变异链球菌葡聚糖的产生和王国间的相互作用。
葡聚糖依赖性生物膜的形成是变异链球菌成为口腔致龋微生物的关键过程。人们对葡聚糖的形成过程进行了深入研究,研究表明,糖基转移酶 GtfB、GtfC 和 GtfD 对于从蔗糖中合成葡聚糖是不可或缺的。在生物膜形成过程中,通过荧光标记可以观察到葡聚糖的产生,而葡聚糖的丰度以及葡聚糖对一般生物膜结构的影响是研究突变体病毒毒力调控的常见表型。在这里,我们描述了一种与葡聚糖产生相关的全新表型,它是由开放阅读框 SMU_848 的突变引起的,该开放阅读框位于编码核糖体相关蛋白的操作子中。这种突变导致在琼脂平板上长期培养后形成的生物膜表面过量产生和积累含葡聚糖的液滴。SMU_848 与噬菌体相关的核糖体蛋白酶 Prp 具有同源性,而 Prp 在金黄色葡萄球菌的核糖体组装过程中对切断核糖体蛋白 L27 的 N 端延伸至关重要。我们对 SMU_848/Prp 进行了进一步鉴定,结果表明该基因的缺失会导致变异葡萄球菌 gtfBC 表达的显著变化。令人惊讶的是,它还对变异棒状杆菌和白色念珠菌之间的相互作用产生了深远影响,而这种相关的双物种相互作用与严重的儿童早期龋齿有牵连。所提供的数据支持 SMU_848/Prp 可能发挥更广泛的作用,可能将其功能扩展到核糖体网络之外,以影响重要的生态过程:重要意义:变异链球菌是口腔生物膜的重要成员,与龋病的发生有关。其主要毒力机制之一是依赖葡聚糖形成生物膜。我们发现了葡聚糖生产调控中的一个新角色 SMU_848,它是一个操作子的一部分,该操作子还编码核糖体蛋白 L27 和 L21。SMU_848编码一种与噬菌体相关的核糖体蛋白酶Prp,它的突变会导致突变体生物膜上含有葡聚糖的液滴大量积聚,这是一种以前未知的表型。进一步的研究扩大了我们对 SMU_848 作用的认识,不仅限于其在葡聚糖生产中的作用,还包括其在王国间相互作用中的重要参与,从而可能在突变体的毒力调控中发挥全球性作用。
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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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