Genetic and biochemical analyses reveal direct interactions between LitR and genes important for Vibrio fischeri physiology, including biofilm production.

IF 3 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2025-08-21 Epub Date: 2025-08-01 DOI:10.1128/jb.00042-25
Brittany L Fung, Chase Mullins, Douglas B Rusch, Elizabeth G Musto, Julia C van Kessel, Karen L Visick
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引用次数: 0

Abstract

Bacteria can link gene expression to population density to promote group behaviors using quorum sensing. Quorum sensing controls a multitude of bacterial processes, such as virulence, motility, and biofilm formation. In Vibrio fischeri, the quorum-sensing-dependent transcription factor LitR inhibits biofilm formation. A previous study showed that LitR inhibits transcription (~1.4-fold) of the bcs locus, which comprises the genes responsible for producing the cellulose polysaccharide. However, beyond that, the mechanism of LitR-mediated inhibition of biofilm formation was unknown. Here, we find that LitR transcriptionally activates pdeV, which encodes a c-di-GMP phosphodiesterase that indirectly promotes cleavage of the large adhesive protein LapV from the surface of V. fischeri, leading to biofilm dispersal. LitR also induces transcription of the gene for sensor kinase VF_A1016, which we determined to be important for biofilm inhibition. Like the loss of LitR, the loss of VF_A1016 increased bcs transcription (~1.6-fold). Through chromatin immunoprecipitation sequencing (ChIP-seq), we found that LitR directly binds to the VF_A1016 and pdeV regulatory region. In total, we identified 147 LitR-binding sites in the genome and confirmed transcriptional control over a subset of these putative regulatory targets. Specifically, we determined that LitR induces transcription of the genes encoding the diguanylate cyclase VF_1200 and the glyoxylate shunt protein AceB and inhibits expression of the putative transcription factor TfoY. These data expand our understanding of LitR-mediated regulation of genes involved in biofilm formation and the physiology of V. fischeri.IMPORTANCEBacteria can coordinate their behaviors on a population level using quorum sensing, a process that results in altered gene regulation. In Vibrio fischeri, the quorum-sensing-regulated transcription factor LitR inhibits the formation of biofilms, communities of attached and protected bacteria, by diminishing the production of cellulose. Here, we determined that LitR controls additional known or putative biofilm factors. We also identified other possible targets of LitR regulation by high-throughput chromatin immunoprecipitation sequencing. This work furthers our understanding of the established connection between quorum sensing and biofilm formation in V. fischeri strain ES114. These findings also have the potential to translate to known pathways in other Vibrios where quorum sensing and biofilm production are linked.

遗传和生化分析揭示了LitR与费氏弧菌生理(包括生物膜生产)重要基因之间的直接相互作用。
细菌可以通过群体感应将基因表达与种群密度联系起来,从而促进群体行为。群体感应控制着大量的细菌过程,如毒力、运动性和生物膜的形成。在费氏弧菌中,群体感应依赖的转录因子LitR抑制生物膜的形成。先前的研究表明,LitR抑制bcs位点的转录(约1.4倍),bcs位点包含负责产生纤维素多糖的基因。然而,除此之外,litr介导的抑制生物膜形成的机制尚不清楚。在这里,我们发现LitR转录激活pdeV, pdeV编码c-di-GMP磷酸二酯酶,间接促进V. fischeri表面大粘附蛋白LapV的裂解,导致生物膜扩散。LitR还诱导了传感器激酶VF_A1016基因的转录,我们确定该基因对生物膜抑制很重要。与LitR的缺失一样,VF_A1016的缺失也增加了bcs的转录(约1.6倍)。通过染色质免疫沉淀测序(ChIP-seq),我们发现LitR直接结合VF_A1016和pdeV调控区。总的来说,我们在基因组中确定了147个litr结合位点,并确认了这些假设的调控靶点的一部分的转录控制。具体来说,我们确定LitR诱导编码二胍酸酯环化酶VF_1200和乙醛酸酯分流蛋白AceB的基因转录,并抑制推定的转录因子TfoY的表达。这些数据扩大了我们对litr介导的参与生物膜形成和费氏弧菌生理的基因调控的理解。细菌可以通过群体感应在群体水平上协调它们的行为,这一过程会导致基因调控的改变。在费氏弧菌中,群体感应调节转录因子LitR通过减少纤维素的产生来抑制生物膜的形成,即附着和受保护细菌的群落。在这里,我们确定LitR控制其他已知或假定的生物膜因素。我们还通过高通量染色质免疫沉淀测序确定了LitR调控的其他可能靶点。这项工作进一步加深了我们对菲氏弧菌ES114群体感应与生物膜形成之间已建立的联系的理解。这些发现也有可能转化为其他弧菌中群体感应和生物膜生产相关的已知途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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