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通过MinION单分子长读长测序描绘插入序列(IS)及IS介导的质粒融合过程

Delineation of IS and IS-Mediated Plasmid Fusion Processes by MinION Single-Molecule Long-Read Sequencing.

作者信息

Chen Kaichao, Xie Miaomiao, Chan Edward Wai-Chi, Chen Sheng

机构信息

Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong SAR, China.

State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China.

出版信息

Front Microbiol. 2022 Feb 7;12:796715. doi: 10.3389/fmicb.2021.796715. eCollection 2021.

Abstract

We recently reported the recovery of a novel IncI1 type conjugative helper plasmid which could target mobile genetic elements (MGE) located in non-conjugative plasmid and form a fusion conjugative plasmid to mediate the horizontal transfer of the non-conjugative plasmid. In this study, interactions between the helper plasmid pSa42-91k and two common MGEs, IS and IS, which were cloned into a pBackZero-T vector, were monitored during the conjugation process to depict the molecular mechanisms underlying the plasmid fusion process mediated by insertion sequence (IS) elements. The MinION single-molecule long-read sequencing technology can dynamically reveal the plasmid recombination events and produce valuable information on genetic polymorphism and plasmid heterogeneity in different multidrug resistance (MDR) encoding bacteria. Such data would facilitate the development of new strategies to control evolution and dissemination of MDR plasmids.

摘要

我们最近报道了一种新型IncI1型接合辅助质粒的发现,该质粒可靶向位于非接合质粒中的移动遗传元件(MGE),并形成融合接合质粒以介导非接合质粒的水平转移。在本研究中,在接合过程中监测了辅助质粒pSa42-91k与两个常见MGE(分别克隆到pBackZero-T载体中的IS和IS)之间的相互作用,以描绘由插入序列(IS)元件介导的质粒融合过程的分子机制。MinION单分子长读长测序技术可以动态揭示质粒重组事件,并提供有关不同多药耐药(MDR)编码细菌中基因多态性和质粒异质性的有价值信息。这些数据将有助于制定控制MDR质粒进化和传播的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/290e/8859459/b95e87dce79f/fmicb-12-796715-g001.jpg

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