Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, Wisconsin.
Division of Infection and Immunity, University College London, London.
Curr Protoc. 2024 Sep;4(9):e70000. doi: 10.1002/cpz1.70000.
The sexually transmitted pathogen, Neisseria gonorrhoeae, undergoes natural transformation at high frequency. This property has led to the rapid dissemination of antibiotic resistance markers and the panmictic structure of the gonococcal population. However, high-frequency transformation also makes N. gonorrhoeae one of the easiest bacterial species to manipulate genetically in the laboratory. Techniques have been developed that result in transformation frequencies >50%, allowing the identification of mutants by screening and without selection. Constructs have been created to take advantage of this high-frequency transformation, facilitating genetic mutation, complementation, and heterologous gene expression. Similar methods have been developed for N. meningitidis and nonpathogenic Neisseria including N. mucosa and N. musculi. Techniques are described for genetic manipulation of N. gonorrhoeae and commensal Neisseria species, as well as for growth of these fastidious organisms. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Spot transformation of Neisseria gonorrhoeae on agar plates Basic Protocol 2: Spot transformation of commensal Neisseria on agar plates Basic Protocol 3: Transformation of Neisseria gonorrhoeae in liquid culture Basic Protocol 4: Electroporation of Neisseria gonorrhoeae Basic Protocol 5: Creation of unmarked mutations using a positive and negative selection cassette Basic Protocol 6: In vitro mutagenesis of Neisseria gonorrhoeae chromosomal DNA using EZ-Tn5 Basic Protocol 7: Chemical mutagenesis Basic Protocol 8: Complementation on the Neisseria gonorrhoeae chromosome Alternate Protocol 1: Complementation with replicating plasmids Alternate Protocol 2: Complementation on the Neisseria musculi or Neisseria mucosa chromosome Basic Protocol 9: Preparation of chromosomal DNA from Neisseria gonorrhoeae grown on solid medium Alternate Protocol 3: Preparation of chromosomal DNA from Neisseria gonorrhoeae grown in broth Support Protocol: Preparing PCR templates from Neisseria gonorrhoeae colonies.
性传播病原体淋病奈瑟菌高频发生自然转化。该特性导致了抗生素耐药标记物的快速传播和淋球菌群体的泛化结构。然而,高频转化也使得淋病奈瑟菌成为实验室中最容易遗传操作的细菌之一。已经开发出的技术可使转化频率>50%,从而无需选择即可通过筛选鉴定突变体。构建了用于利用这种高频转化的构建体,促进了遗传突变、互补和异源基因表达。类似的方法已应用于脑膜炎奈瑟菌和非致病性奈瑟菌,包括粘膜奈瑟菌和肌肉奈瑟菌。本文描述了用于淋病奈瑟菌和共生奈瑟菌(包括粘膜奈瑟菌和肌肉奈瑟菌)遗传操作的技术,以及这些苛刻生物体的生长方法。© 2024 作者。本文由 Wiley Periodicals LLC 出版。 基本方案 1:淋病奈瑟菌在琼脂平板上的点转化 基本方案 2:共生奈瑟菌在琼脂平板上的点转化 基本方案 3:淋病奈瑟菌在液体培养基中的转化 基本方案 4:淋病奈瑟菌的电穿孔 基本方案 5:使用正、负选择盒创建无标记突变 基本方案 6:使用 EZ-Tn5 对淋病奈瑟菌染色体 DNA 进行体外诱变 基本方案 7:化学诱变 基本方案 8:淋病奈瑟菌染色体上的互补作用 备选方案 1:使用复制质粒进行互补 备选方案 2:在奈瑟菌肌肉或奈瑟菌粘膜染色体上进行互补 基本方案 9:从固体培养基中生长的淋病奈瑟菌中制备染色体 DNA 备选方案 3:从肉汤中生长的淋病奈瑟菌中制备染色体 DNA 基本方案 10:从淋病奈瑟菌菌落中制备 PCR 模板。