肺炎克雷伯氏菌 NTUH-K2044 中铁吸收调节因子对 yersiniabactin 受体 fyuA 基因的转录调控

IF 3.5 4区 生物学 Q2 MICROBIOLOGY Journal of Basic Microbiology Pub Date : 2024-04-28 DOI:10.1002/jobm.202400001
Qian Yu, Hailin Li, Ling Du, Lifei Shen, Jiaxue Zhang, Lingyue Yuan, Huang Yao, Hong Xiao, Qunhua Bai, Yan Jia, Jingfu Qiu, Yingli Li
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引用次数: 0

摘要

铁吸收调节因子(Fur)是一种影响肺炎克雷伯氏菌毒力基因表达的全局调节因子。生物信息学分析表明,Fur 可能通过耶氏双歧杆菌素受体基因 fyuA 上游的调节框参与铁的获取。为了观察基因 fyuA 对肺炎双球菌毒力的影响,研究人员构建了基因 fyuA 基因敲除菌株和互补菌株,并进行了一系列表型实验,包括铬偶氮呋喃 S(CAS)检测、结晶紫染色和蜡蛾毒力实验。为了研究Fur与基因fyuA之间的调控关系,采用了绿色荧光蛋白(GFP)报告基因融合实验、实时定量反转录聚合酶链式反应(RT-qPCR)、凝胶迁移实验(EMSA)和DNase I足印实验来阐明Fur对fyuA的调控机制。CAS 检测发现,fyuA 基因可影响肺炎双球菌中铁载体的生成。水晶紫染色实验表明,fyuA 能积极影响生物膜的形成。蜡蛾毒力实验表明,缺失 fyuA 可削弱细菌的毒力。GFP 报告基因融合实验和 RT-qPCR 分析表明,在铁充足的环境中,Fur 负向调控 fyuA 的表达。EMSA实验表明,Fur可直接与fyuA的启动子区域结合,DNase I足迹分析进一步确定了特异的结合位点序列。研究表明,Fur通过与基因启动子区上游结合,负向调控fyuA的转录表达,进而影响肺炎双球菌的毒力。
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Transcriptional regulation of the yersiniabactin receptor fyuA gene by the ferric uptake regulator in Klebsiella pneumoniae NTUH-K2044

The ferric uptake regulator (Fur) is a global regulator that influences the expression of virulence genes in Klebsiella pneumoniae. Bioinformatics analysis suggests Fur may involve in iron acquisition via the identified regulatory box upstream of the yersiniabactin receptor gene fyuA. To observe the impact of the gene fyuA on the virulence of K. pneumoniae, the gene fyuA knockout strain and complementation strain were constructed and then conducted a series of phenotypic experiments including chrome azurol S (CAS) detection, crystal violet staining, and wax moth virulence experiment. To examine the regulatory relationship between Fur and the gene fyuA, green fluorescent protein (GFP) reporter gene fusion assay, real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR), gel migration assay (EMSA), and DNase I footprinting assay were used to clarify the regulatory mechanism of Fur on fyuA. CAS detection revealed that the gene fyuA could affect the generation of iron carriers in K. pneumoniae. Crystal violet staining experiment showed that fyuA could positively influence biofilm formation. Wax moth virulence experiment indicated that the deletion of the fyuA could weaken bacterial virulence. GFP reporter gene fusion experiment and RT-qPCR analysis revealed that Fur negatively regulated the expression of fyuA in iron-sufficient environment. EMSA experiment demonstrated that Fur could directly bind to the promoter region of fyuA, and DNase I footprinting assay further identified the specific binding site sequences. The study showed that Fur negatively regulated the transcriptional expression of fyuA by binding to upstream of the gene promoter region, and then affected the virulence of K. pneumoniae.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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