School of Dentistry and Institute for Microbiology and Infection, University of Birmingham, Birmingham, UK.
Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, Victoria, Australia 3800.
Microbiol Spectr. 2019 May;7(3). doi: 10.1128/microbiolspec.GPP3-0040-2018.
The past 10 years have been revolutionary for clostridial genetics. The rise of next-generation sequencing led to the availability of annotated whole-genome sequences of the important pathogenic clostridia: , () , and , but also () and . These sequences were a prerequisite for the development of functional, sophisticated genetic tools for the pathogenic clostridia. A breakthrough came in the early 2000s with the development of TargeTron-based technologies specific for the clostridia, such as ClosTron, an insertional gene inactivation tool. The following years saw a plethora of new technologies being developed, mostly for , but also for other members of the genus, including . A range of tools is now available, allowing researchers to precisely delete genes, change single nucleotides in the genome, complement deletions, integrate novel DNA into genomes, or overexpress genes. There are tools for forward genetics, including an inducible transposon mutagenesis system for . As the latest addition to the tool kit, clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 technologies have also been adopted for the construction of single and multiple gene deletions in . This article summarizes the key genetic technologies available to manipulate, study, and understand the pathogenic clostridia.
过去 10 年见证了梭菌遗传学的革命性发展。新一代测序技术的兴起使得重要病原性梭菌的注释全基因组序列得以问世,包括、、和,但也包括和。这些序列是为病原性梭菌开发功能性、复杂遗传工具的前提。21 世纪初,基于 TargeTron 的梭菌特异性技术(如 ClosTron,一种插入基因失活工具)的发展取得了突破。随后的几年里,大量新技术得以开发,这些技术主要针对,但也针对该属的其他成员,包括。现在有一系列工具可供使用,使研究人员能够精确地删除基因、改变基因组中的单个核苷酸、互补缺失、将新的 DNA 整合到基因组中或过表达基因。有用于正向遗传学的工具,包括用于的诱导转座子诱变系统。作为工具包的最新补充,成簇规律间隔短回文重复(CRISPR)-Cas9 技术也已被用于在构建单基因和多基因缺失。本文总结了用于操纵、研究和理解病原性梭菌的关键遗传技术。