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用于II类芽孢和孢子形成研究的基于CRISPR-Cas9的工具包

CRISPR-Cas9-Based Toolkit for Group II Spore and Sporulation Research.

作者信息

Mertaoja Anna, Nowakowska Maria B, Mascher Gerald, Heljanko Viivi, Groothuis Daphne, Minton Nigel P, Lindström Miia

机构信息

Department of Food Hygiene and Environmental Health, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.

Clostridia Research Group, BBSRC/EPSRC Synthetic Biology Research Centre (SBRC), Biodiscovery Institute, School of Life Sciences, University of Nottingham, Nottingham, United Kingdom.

出版信息

Front Microbiol. 2021 Jan 27;12:617269. doi: 10.3389/fmicb.2021.617269. eCollection 2021.

Abstract

The spores of Group II strains pose a significant threat to the safety of modern packaged foods due to the risk of their survival in pasteurization and their ability to germinate into neurotoxigenic cultures at refrigeration temperatures. Moreover, spores are the infectious agents in wound botulism, infant botulism, and intestinal toxemia in adults. The identification of factors that contribute to spore formation is, therefore, essential to the development of strategies to control related health risks. Accordingly, development of a straightforward and versatile gene manipulation tool and an efficient sporulation-promoting medium is pivotal. Our strategy was to employ CRISPR-Cas9 and homology-directed repair (HDR) to replace targeted genes with mutant alleles incorporating a unique 24-nt "bookmark" sequence that could act as a single guide RNA (sgRNA) target for Cas9. Following the generation of the sporulation mutant, the presence of the bookmark allowed rapid generation of a complemented strain, in which the mutant allele was replaced with a functional copy of the deleted gene using CRISPR-Cas9 and the requisite sgRNA. Then, we selected the most appropriate medium for sporulation studies in Group II strains by measuring the efficiency of spore formation in seven different media. The most effective medium was exploited to confirm the involvement of a candidate gene in the sporulation process. Using the devised sporulation medium, subsequent comparisons of the sporulation efficiency of the wild type (WT), mutant and "bookmark"-complemented strain allowed the assignment of any defective sporulation phenotype to the mutation made. As a strain generated by complementation with the WT gene in the original locus would be indistinguishable from the parental strain, the gene utilized in complementation studies was altered to contain a unique "watermark" through the introduction of silent nucleotide changes. The mutagenesis system and the devised sporulation medium provide a solid basis for gaining a deeper understanding of spore formation in , a prerequisite for the development of novel strategies for spore control and related food safety and public health risk management.

摘要

II 组菌株的孢子对现代包装食品的安全构成重大威胁,因为它们有在巴氏杀菌过程中存活的风险,并且能够在冷藏温度下发芽成为产生神经毒素的培养物。此外,孢子是伤口肉毒中毒、婴儿肉毒中毒和成人肠道毒血症的感染因子。因此,确定有助于孢子形成的因素对于制定控制相关健康风险的策略至关重要。相应地,开发一种简单通用的基因操作工具和一种高效的促进孢子形成的培养基至关重要。我们的策略是利用 CRISPR-Cas9 和同源定向修复(HDR),用包含独特的 24 个核苷酸“书签”序列的突变等位基因替换目标基因,该序列可作为 Cas9 的单向导 RNA(sgRNA)靶点。在产生孢子形成突变体后,书签的存在使得能够快速产生互补菌株,其中使用 CRISPR-Cas9 和必需的 sgRNA 将突变等位基因替换为缺失基因的功能拷贝。然后,我们通过测量七种不同培养基中孢子形成的效率,选择了最适合 II 组菌株孢子形成研究的培养基。利用最有效的培养基来确认候选基因在孢子形成过程中的作用。使用设计的孢子形成培养基,随后对野生型(WT)、突变体和“书签”互补菌株的孢子形成效率进行比较,可以将任何有缺陷的孢子形成表型归因于所做的突变。由于在原始位点与 WT 基因互补产生的菌株与亲本菌株无法区分,因此通过引入沉默核苷酸变化,将用于互补研究的基因改变为包含独特的“水印”。诱变系统和设计的孢子形成培养基为更深入了解[具体菌株名称未给出]中的孢子形成提供了坚实基础,这是开发孢子控制新策略以及相关食品安全和公共卫生风险管理的先决条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2c/7873358/ede3b02c1638/fmicb-12-617269-g001.jpg

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