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肠出血性大肠杆菌 O157:H7 型 VI 型分泌系统分歧启动子转录活性的特征。

Characterization of transcriptional activities at a divergent promoter of the type VI secretion system in enterohemorrhagic Escherichia coli O157:H7.

机构信息

College of Veterinary Medicine & Institute of Veterinary Science, Kangwon National University, Chuncheon, Gangwon, 24341, Korea.

出版信息

J Microbiol. 2022 Sep;60(9):928-934. doi: 10.1007/s12275-022-2109-9. Epub 2022 Aug 19.

Abstract

The type VI secretion system (T6SS) is a novel secretion system found in many Gram-negative bacteria that plays a role in bacterial competition, virulence, and host immune evasion. The enterohemorrhagic Escherichia coli (EHEC) O157:H7 strain EDL933 has a single functional T6SS gene cluster. In this study, we attempted to characterize the transcriptional pattern of the T6SS effector gene Z0264 in EDL933. Transcriptional analyses showed that Z0264 and other T6SS genes were transcribed in vitro in a growth-phase-dependent manner, but Z0264 was not secreted in the rich medium. Using adapter- and radioactivity-free transcription start site analysis, we identified an overlapping divergent promoter between Z0264 and Z0265. A β-galactosidase assay with truncated promoter regions showed that the divergent promoter is functional. In addition, we demonstrated the role of H-NS as a repressor in the transcription of Z0264. Notably, the cDNA PCR assay showed that the mRNA transcript from the Z0264 promoter did not include the entire main T6SS cluster, suggesting segmented gene expression by multiple promoters in the T6SS cluster. In conclusion, we identified a divergent promoter for Z0264 located in the T6SS cluster of EDL933 and characterized its in vitro transcriptional activity during growth. Our findings provide insights and a preliminary understanding of the regulatory mechanisms underlying T6SS transcription.

摘要

VI 型分泌系统(T6SS)是一种新型的分泌系统,存在于许多革兰氏阴性菌中,在细菌竞争、毒力和宿主免疫逃避中发挥作用。肠出血性大肠杆菌(EHEC)O157:H7 菌株 EDL933 具有单个功能 T6SS 基因簇。在本研究中,我们试图描述 EDL933 中 T6SS 效应基因 Z0264 的转录模式。转录分析表明,Z0264 和其他 T6SS 基因在体外以生长阶段依赖的方式转录,但 Z0264 未在丰富培养基中分泌。使用适配器和放射性自由转录起始位点分析,我们在 Z0264 和 Z0265 之间鉴定了一个重叠的发散启动子。具有截断启动子区域的β-半乳糖苷酶测定表明发散启动子是功能性的。此外,我们证明了 H-NS 作为 Z0264 转录的抑制剂的作用。值得注意的是,cDNA PCR 检测表明,来自 Z0264 启动子的 mRNA 转录物不包括整个主要 T6SS 簇,这表明 T6SS 簇中的多个启动子可进行分段基因表达。总之,我们确定了 EDL933 的 T6SS 簇中 Z0264 的发散启动子,并对其在生长过程中的体外转录活性进行了特征描述。我们的研究结果为 T6SS 转录的调控机制提供了见解和初步理解。

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