通过自诱导剂-2的群体感应促进两歧双歧杆菌PRL2010的定植和宿主适应。

IF 5.2 2区 生物学
Francesca Turroni, Chiara Tarracchini, Gabriele Andrea Lugli, Laura Maria Vergna, Giulia Alessandri, Sonia Mirjam Rizzo, Massimiliano G. Bianchi, Tom Coenye, Emanuele Selleri, Ovidio Bussolati, Douwe van Sinderen, Marco Ventura
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引用次数: 0

摘要

自诱导剂-2 (AI-2)是一种关键的信号分子,在许多细菌中,它通过群体感应的过程调节基因表达,以响应种群密度,促进物种间的交流。虽然这种信号机制已在革兰氏阴性菌中得到广泛研究,但其在双歧杆菌属中的作用仍知之甚少。在这项研究中,进行了一项计算机分析,以检查双歧杆菌基因组中luxS基因的分布,该基因编码合成AI-2前体的酶。我们的分析显示luxS普遍存在于所有公开的双歧杆菌基因组中。为了探索luxS的功能意义,我们对两歧双歧杆菌模型菌株PRL2010及其等基因luxS插入突变体进行了基因表达谱分析,这两种菌株都在模拟人类肠道环境的培养基中生长。RNA测序结果表明,luxS的破坏损害了突变菌株(i)与宿主相互作用和通信的能力,(ii)运输糖,(iii)内化钾和铁,以及(iv)应对应激条件的能力。总的来说,这些发现强调了AI-2在促进定植和确保PRL2010在人类肠道竞争生态系统中的持久性方面的关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Quorum Sensing via Autoinducer-2 Promotes Colonisation and Host Adaptation in B. bifidum PRL2010

Autoinducer-2 (AI-2) is a key signalling molecule that in many bacteria facilitates interspecies communication by regulating gene expression in response to population density through a process known as quorum sensing. While this signalling mechanism has been extensively studied in Gram-negative bacteria, its role in the genus Bifidobacterium remains poorly understood. In this study, an in silico analysis was conducted to examine the distribution of the luxS gene, which encodes the enzyme that synthesises the AI-2 precursor, across Bifidobacterium genomes. Our analysis revealed that luxS is ubiquitously present in all publicly available bifidobacterial genomes. To explore the functional implications of luxS, gene expression profiling was performed on the model strain B. bifidum PRL2010 and its isogenic luxS insertion mutant, both grown in a medium simulating the human gut environment. RNA sequencing results indicated that disruption of luxS impairs the mutant strain's ability to (i) interact and communicate with the host, (ii) transport sugars, (iii) internalise potassium and iron, and (iv) cope with stress conditions. Collectively, these findings highlight the crucial role of AI-2 in promoting colonisation and ensuring the persistence of PRL2010 within the competitive ecosystem of the human gut.

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来源期刊
Microbial Biotechnology
Microbial Biotechnology Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
11.20
自引率
3.50%
发文量
162
审稿时长
1 months
期刊介绍: Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes
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