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肺炎克雷伯氏菌的遗传操作。

Genetic Manipulation of Klebsiella pneumoniae.

机构信息

Department of Medical Microbiology and Immunology, The University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.

出版信息

Curr Protoc. 2023 Oct;3(10):e912. doi: 10.1002/cpz1.912.

Abstract

Klebsiella pneumoniae is a Gram-negative, rod-shaped bacterium commonly found in the human intestine. Although it typically exists as part of the normal flora, it can also cause healthcare-associated infections with severe consequences. Understanding the specific genes responsible for its virulence through genetic manipulation is crucial for potential therapeutic interventions. However, manipulating K. pneumoniae presents challenges due to its exopolysaccharide capsule. This article presents a comprehensive collection of protocols designed to facilitate the genetic manipulation of K. pneumoniae. By following these protocols, researchers will acquire the necessary skills to prepare electrocompetent cells, utilize electroporation for efficient plasmid DNA introduction, construct isogenic mutants using the λ Red recombinase system, and generate a complementation vector for restoring the phenotypic traits of knockout strains. These protocols provide valuable tools and techniques to navigate the intricacies associated with studying and modifying K. pneumoniae. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Preparing electrocompetent K. pneumoniae cells Alternate Protocol 1: Preparing electrocompetent K. pneumoniae cells for recombineering Basic Protocol 2: Transforming K. pneumoniae using electroporation Basic Protocol 3: Constructing isogenic mutants in K. pneumoniae using the λ Red recombinase system Support Protocol 1: Confirming a knockout via colony PCR Support Protocol 2: Verifying absence of secondary mutations Basic Protocol 4: Generating unmarked knockout mutants in K. pneumoniae using the pFLP plasmid Basic Protocol 5: Constructing a complementation vector for K. pneumoniae.

摘要

肺炎克雷伯菌是一种革兰氏阴性、杆状细菌,通常存在于人类肠道中。虽然它通常作为正常菌群的一部分存在,但也可能引起严重后果的医疗保健相关感染。通过遗传操作了解导致其毒力的特定基因对于潜在的治疗干预至关重要。然而,由于其外多糖胶囊,操纵肺炎克雷伯菌存在挑战。本文提供了一套全面的方案,旨在促进肺炎克雷伯菌的遗传操作。通过遵循这些方案,研究人员将获得制备电感受态细胞、利用电穿孔高效引入质粒 DNA、使用 λ Red 重组酶系统构建同源突变体以及生成用于恢复敲除菌株表型特征的互补载体的必要技能。这些方案为研究和修饰肺炎克雷伯菌提供了有价值的工具和技术。© 2023 作者。Wiley Periodicals LLC 出版的《当代方案》。基本方案 1:制备电感受态肺炎克雷伯菌细胞备选方案 1:准备用于重组的电感受态肺炎克雷伯菌细胞基本方案 2:通过电穿孔转化肺炎克雷伯菌基本方案 3:使用 λ Red 重组酶系统在肺炎克雷伯菌中构建同源突变体支持方案 1:通过菌落 PCR 确认敲除支持方案 2:验证不存在二次突变基本方案 4:使用 pFLP 质粒在肺炎克雷伯菌中生成无标记敲除突变体基本方案 5:构建肺炎克雷伯菌的互补载体。

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