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Novel Probiotic Mechanisms of the Oral Bacterium Streptococcus sp. A12 as Explored with Functional Genomics

机译:口腔细菌链球菌属的新型益生菌机制A12 与功能基因组学的探索

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摘要

Health-associated biofilms in the oral cavity are composed of a diverse group of microbial species that can foster an environment that is less favorable for the outgrowth of dental caries pathogens, like Streptococcus mutans. A novel oral bacterium, designated Streptococcus A12, was previously isolated from supragingival dental plaque of a caries-free individual and was shown to interfere potently with the growth and virulence properties of S. mutans. In this study, we applied functional genomics to begin to identify molecular mechanisms used by A12 to antagonize, and to resist the antagonistic factors of, S. mutans. Using bioinformatics, genes that could encode factors that enhance the ability of A12 to compete with S. mutans were identified. Selected genes, designated potential competitive factors (pcf), were deleted. Certain mutant derivatives showed a reduced capacity to compete with S. mutans compared to that of the parental strain. The A12 pcfO mutant lost the ability to inhibit comX-inducing peptide (XIP) signaling by S. mutans, while mutants with changes in the pcfFEG locus were impaired in sensing of, and were more sensitive to, the lantibiotic nisin. Loss of PcfV, annotated as a colicin V biosynthetic protein, resulted in diminished antagonism of S. mutans. Collectively, the data provide new insights into the complexities and variety of factors that affect biofilm ecology and virulence. Continued exploration of the genomic and physiological factors that distinguish commensals from truly beneficial members of the oral microbiota will lead to a better understanding of the microbiome and new approaches to promote oral health.
机译:口腔中与健康相关的生物膜由一组不同的微生物物种组成,这些微生物物种可以营造不利于龋齿病原体(如变形链球菌)生长的环境。一种新型口腔细菌,称为链球菌A12,先前从无龋齿个体的龈上牙菌斑中分离出来,并被证明可以有效干扰变形链球菌的生长和毒力特性。在这项研究中,我们应用功能基因组学开始鉴定 A12 用于拮抗和抵抗变形链球菌拮抗因子的分子机制。利用生物信息学,鉴定了可以编码增强 A12 与变形链球菌竞争能力的因子的基因。选定的基因,指定为潜在竞争因子(pcf),被删除。与亲本菌株相比,某些突变衍生物显示出与变形链球菌竞争的能力降低。A12 pcfO突变体失去了抑制变形链球菌抑制comX诱导肽(XIP)信号传导的能力,而pcfFEG位点发生变化的突变体对兰氏抗生素乳链菌肽的感知受损,并且对乳酸链菌肽更敏感。注释为大肠杆菌素 V 生物合成蛋白的 PcfV 的丢失导致变形链球菌的拮抗作用减弱。总的来说,这些数据为影响生物膜生态和毒力的复杂性和多样性因素提供了新的见解。继续探索将共生体与口腔微生物群中真正有益的成员区分开来的基因组和生理因素将导致对微生物组的更好理解和促进口腔健康的新方法。

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