Brittany L Fung, Elizabeth G Musto, Linsey Kathure Mugambi, Madison L Lange, Jovanka Tepavcevic, Karen L Visick
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We found instead that the C/A change engendered a new transcriptional start site. Furthermore, the C/A change was sufficient to robustly promote <i>syp</i>-dependent biofilm formation dependent on HahK and SypG but only partially dependent on the central regulator SypF. Rather, the residual biofilm formation in the absence of SypF relied on the luminescence regulator LuxU. Consistent with its ability to produce <i>syp</i>-dependent biofilms, a Δ<i>sypF</i> mutant that carried the C/A-<i>hahK</i> allele outcompeted its Δ<i>sypF</i> parent for squid colonization. Finally, bioinformatic analyses of the <i>hnoX</i> promoter region in various <i>V. fischeri</i> isolates revealed that most contained G or C nucleotides lacking in ES114, indicating an evolutionary divergence between different isolates. Together, these findings uncover the ability of HahK to signal through both SypF and LuxU to induce <i>syp</i>-dependent biofilm formation and host colonization, thus advancing our understanding of the regulators that control <i>syp</i>-dependent biofilm formation by <i>V. fischeri</i>.IMPORTANCEBiofilms promote the attachment of bacteria to each other and to surfaces. For <i>Vibrio fischeri</i>, biofilm formation dependent on the symbiosis polysaccharide (<i>syp</i>) locus promotes colonization of its symbiotic host. Multiple two-component regulators, including the central sensor kinase SypF and nitric oxide/HnoX-controlled sensor kinase HahK, induce SYP production. Here, we identify a C/A change in the <i>hnoX-hahK</i> regulatory region that substantially increases its transcription and SYP-dependent biofilm formation. We further determined that HahK signals through both SypF and the luminescence regulator LuxU to promote biofilm formation and host colonization. Our findings thus provide insight into the regulatory crossover between two major pathways, quorum sensing-controlled luminescence and biofilm formation, in <i>V. fischeri</i>.</p>","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":" ","pages":"e0013125"},"PeriodicalIF":3.0000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12369376/pdf/","citationCount":"0","resultStr":"{\"title\":\"A single point mutation is sufficient to drive <i>syp</i>-dependent biofilm formation and promote colonization by <i>Vibrio fischeri</i>.\",\"authors\":\"Brittany L Fung, Elizabeth G Musto, Linsey Kathure Mugambi, Madison L Lange, Jovanka Tepavcevic, Karen L Visick\",\"doi\":\"10.1128/jb.00131-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Symbiotic colonization by <i>Vibrio fischeri</i> relies on the <i>syp</i> gene cluster, which encodes proteins predicted to synthesize and export a polysaccharide, SYP, that functions in cell-cell adherence. In strain ES114, four two-component sensor kinase/phosphatases, including central regulator SypF and the nitric oxide/HnoX-controlled HahK, dictate the activities of two response regulators, SypG and SypE, which in turn control SYP production. Here, we report that a single nucleotide change (C/A) upstream of the <i>hnoX-hahK</i> operon caused a substantial 80-fold increase in its transcription. While a search for negative regulators yielded Zur (zinc uptake regulator), loss of Zur only modestly (approximately threefold) increased transcription. We found instead that the C/A change engendered a new transcriptional start site. Furthermore, the C/A change was sufficient to robustly promote <i>syp</i>-dependent biofilm formation dependent on HahK and SypG but only partially dependent on the central regulator SypF. Rather, the residual biofilm formation in the absence of SypF relied on the luminescence regulator LuxU. Consistent with its ability to produce <i>syp</i>-dependent biofilms, a Δ<i>sypF</i> mutant that carried the C/A-<i>hahK</i> allele outcompeted its Δ<i>sypF</i> parent for squid colonization. Finally, bioinformatic analyses of the <i>hnoX</i> promoter region in various <i>V. fischeri</i> isolates revealed that most contained G or C nucleotides lacking in ES114, indicating an evolutionary divergence between different isolates. Together, these findings uncover the ability of HahK to signal through both SypF and LuxU to induce <i>syp</i>-dependent biofilm formation and host colonization, thus advancing our understanding of the regulators that control <i>syp</i>-dependent biofilm formation by <i>V. fischeri</i>.IMPORTANCEBiofilms promote the attachment of bacteria to each other and to surfaces. For <i>Vibrio fischeri</i>, biofilm formation dependent on the symbiosis polysaccharide (<i>syp</i>) locus promotes colonization of its symbiotic host. 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引用次数: 0
摘要
费氏弧菌的共生定植依赖于syp基因簇,该基因簇编码蛋白质,预计合成和输出多糖syp, syp在细胞-细胞粘附中起作用。在菌株ES114中,四种双组分传感器激酶/磷酸酶,包括中央调节剂SypF和一氧化氮/ hnox控制的HahK,决定两种反应调节剂SypG和SypE的活性,进而控制SYP的产生。在这里,我们报道了hnoX-hahK操纵子上游的单个核苷酸变化(C/ a)导致其转录增加了80倍。虽然寻找负调节因子产生了Zur(锌摄取调节因子),但Zur的损失仅适度(大约三倍)增加了转录。相反,我们发现C/A的改变产生了一个新的转录起始位点。此外,C/A的变化足以促进依赖HahK和SypG的syp依赖性生物膜的形成,但仅部分依赖中枢调节因子SypF。相反,在没有SypF的情况下,残留生物膜的形成依赖于发光调节剂LuxU。与其产生依赖于syp的生物膜的能力相一致,携带C/ a - hahk等位基因的ΔsypF突变体在乌贼定植方面胜过了其ΔsypF亲本。最后,对不同费氏弧菌分离株的hnoX启动子区进行生物信息学分析,发现大多数菌株含有ES114中缺乏的G或C核苷酸,表明不同分离株之间存在进化差异。总之,这些发现揭示了HahK通过SypF和LuxU信号诱导syp依赖性生物膜形成和宿主定植的能力,从而促进了我们对控制费氏弧菌syp依赖性生物膜形成的调节因子的理解。重要意义生物膜促进细菌之间和表面的附着。对于费氏弧菌,依赖于共生多糖(syp)位点的生物膜形成促进其共生宿主的定植。多种双组分调节因子,包括中央传感器激酶SypF和一氧化氮/ hnox控制的传感器激酶HahK,诱导SYP的产生。在这里,我们发现hnoX-hahK调控区域的C/ a变化大大增加了其转录和syp依赖性生物膜的形成。我们进一步确定HahK通过SypF和发光调节因子LuxU发出信号,促进生物膜的形成和宿主定植。因此,我们的研究结果为fischeri中群体感应控制的发光和生物膜形成这两个主要途径之间的调控交叉提供了见解。
A single point mutation is sufficient to drive syp-dependent biofilm formation and promote colonization by Vibrio fischeri.
Symbiotic colonization by Vibrio fischeri relies on the syp gene cluster, which encodes proteins predicted to synthesize and export a polysaccharide, SYP, that functions in cell-cell adherence. In strain ES114, four two-component sensor kinase/phosphatases, including central regulator SypF and the nitric oxide/HnoX-controlled HahK, dictate the activities of two response regulators, SypG and SypE, which in turn control SYP production. Here, we report that a single nucleotide change (C/A) upstream of the hnoX-hahK operon caused a substantial 80-fold increase in its transcription. While a search for negative regulators yielded Zur (zinc uptake regulator), loss of Zur only modestly (approximately threefold) increased transcription. We found instead that the C/A change engendered a new transcriptional start site. Furthermore, the C/A change was sufficient to robustly promote syp-dependent biofilm formation dependent on HahK and SypG but only partially dependent on the central regulator SypF. Rather, the residual biofilm formation in the absence of SypF relied on the luminescence regulator LuxU. Consistent with its ability to produce syp-dependent biofilms, a ΔsypF mutant that carried the C/A-hahK allele outcompeted its ΔsypF parent for squid colonization. Finally, bioinformatic analyses of the hnoX promoter region in various V. fischeri isolates revealed that most contained G or C nucleotides lacking in ES114, indicating an evolutionary divergence between different isolates. Together, these findings uncover the ability of HahK to signal through both SypF and LuxU to induce syp-dependent biofilm formation and host colonization, thus advancing our understanding of the regulators that control syp-dependent biofilm formation by V. fischeri.IMPORTANCEBiofilms promote the attachment of bacteria to each other and to surfaces. For Vibrio fischeri, biofilm formation dependent on the symbiosis polysaccharide (syp) locus promotes colonization of its symbiotic host. Multiple two-component regulators, including the central sensor kinase SypF and nitric oxide/HnoX-controlled sensor kinase HahK, induce SYP production. Here, we identify a C/A change in the hnoX-hahK regulatory region that substantially increases its transcription and SYP-dependent biofilm formation. We further determined that HahK signals through both SypF and the luminescence regulator LuxU to promote biofilm formation and host colonization. Our findings thus provide insight into the regulatory crossover between two major pathways, quorum sensing-controlled luminescence and biofilm formation, in V. fischeri.
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.