环境pH值控制人类益生菌唾液链球菌的抗菌生产。

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Dieu Linh Nguyen, Subhasree Saha, Aswin Thacharodi, Bharat Bhushan Singh, Sonali Mitra, Hackwon Do, Muthiah Kumaraswami
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引用次数: 0

摘要

唾液链球菌K12 (SAL)是一种用于治疗或预防由人类病原体引起的口腔感染的口服益生菌。SAL至少产生三种抗菌剂来发挥其抗菌活性,即唾液毒素A和唾液毒素B,以及新发现的唾液毒素。唾液分泌素的产生是由聚酮/非核糖体肽合成酶混合生物合成基因簇(BGC)催化的,称为sar-BGC。在体外和体内SAL生长过程中,sar-BGC的表达和唾液分泌素的产生是短暂的,这可能会对SAL益生菌的功效产生负面影响。为了了解瞬时sar-BGC表达的分子基础,我们评估了环境pH对sar-BGC表达的影响。我们发现环境酸化是通过诱导sar-BGC表达促进唾液分泌素抗菌活性和产生的关键因素。我们进一步表明,酸性pH值直接影响控制sar-BGC表达的群体感应系统。在环境酸化过程中,SAL细胞质被酸化,这是由细胞质转录调节因子NrpR中ph敏感的组氨酸开关感知的。胞质酸化过程中组氨酸的质子化促进了NrpR与其同源细胞间信号肽NIP之间的高亲和力相互作用,从而导致sar-BGC表达上调。总的来说,我们的研究结果表明,SAL在有利于其抗菌活性的环境中使用复杂的调节机制来协调唾液分泌素的产生。重要性:益生菌是对抗细菌感染的重要工具。益生菌通过几种机制发挥其抗菌活性,包括抗菌生产。然而,益生菌在体内和体外抑制病原菌生长的效果存在差异。了解影响抗菌药物生产和活性的宿主和环境因素对提高益生菌的功效至关重要。在这项研究中,我们发现人类口腔益生菌唾液链球菌K12产生的抗菌唾液分泌素在酸性ph下具有活性。我们进一步阐明了唾液链球菌协调唾液分泌素与环境酸化相一致的分子机制,从而最大限度地提高了唾液分泌素的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Environmental pH controls antimicrobial production by human probiotic Streptococcus salivarius.

Streptococcus salivarius K12 (SAL) is an oral probiotic used to treat or prevent oral infections caused by human pathogens. SAL produces at least three antimicrobials to exert its antimicrobial activity, namely, salivaricin A and salivaricin B, and the newly identified salivabactin. Salivabactin production is catalyzed by a polyketide/non-ribosomal peptide synthase hybrid biosynthetic gene cluster (BGC), termed as sar-BGC. The sar-BGC expression and salivabactin production are transient during SAL growth in vitro and in vivo, which may negatively impact SAL probiotic efficacy. To understand the molecular basis for transient sar-BGC expression, we assessed the impact of environmental pH on sar-BGC expression. We found that environmental acidification is a critical factor in promoting salivabactin antimicrobial activity and production by inducing sar-BGC expression. We further showed that acidic pH directly influences the quorum-sensing system that controls sar-BGC expression. During environmental acidification, SAL cytosol is acidified, which is sensed by a pH-sensitive histidine switch in the cytosolic transcription regulator, NrpR. The protonation of histidine during cytosolic acidification promotes high-affinity interactions between NrpR and its cognate intercellular signaling peptide, NIP, which leads to upregulation of sar-BGC expression. Collectively, our results indicate that SAL uses a sophisticated regulatory mechanism to orchestrate salivabactin production in an environment that is conducive to its antimicrobial activity.

Importance: Probiotic bacteria are important tools in combating bacterial infections. Probiotics exert their antimicrobial activity via several mechanisms, including antimicrobial production. However, discrepancies exist between the in vitro and in vivo efficacies of probiotics in inhibiting pathogen growth. Understanding the host and environmental factors that influence antimicrobial production and activity is critical for improving probiotic efficacy. In this study, we showed that the antimicrobial salivabactin produced by human oral probiotic Streptococcus salivarius K12 is active at acidic pH. We further elucidated the molecular mechanism by which S. salivarius coordinates salivabactin production in concert with environmental acidification, thereby maximizing salivabactin antimicrobial activity.

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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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