Decoding gene essentiality in Streptococcus suis using Tn-seq and genome-scale metabolic modeling.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-10-07 Epub Date: 2025-08-14 DOI:10.1128/spectrum.01303-25
Yaoqin Hong
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引用次数: 0

Abstract

High-throughput transposon mutagenesis methods, such as transposon sequencing, are powerful tools for genome-wide identification of essential and conditionally essential genes in bacterial pathogens. In a recent study, Y. Zhang, R.Gong, M.Liang, L.Zhang, et al. (Microbiol Spectr 13:e0279124, 2025, https://doi.org/10.1128/spectrum.02791-24) applied Himar1-based Tn-seq to Streptococcus suis, generating a relatively dense mutant library, in combination with genome-scale metabolic modeling, to identify 244 candidate essential genes. Aside from the well-characterized antibiotic targets, there are several novel candidates currently being explored for drug development against other critical pathogens, and a number of previously uncharacterized potential targets were uncovered in classical model organisms. The study highlights the value of high-throughput transposon mutagenesis and genome-scale metabolic modeling in a less-characterized zoonotic pathogen and contributes important genetic insights that may inform future antimicrobial strategies.

Abstract Image

Abstract Image

利用n-seq和基因组尺度代谢模型解码猪链球菌基因的必要性。
高通量转座子诱变方法,如转座子测序,是全基因组鉴定细菌病原体必需基因和条件必需基因的有力工具。在最近的一项研究中,Y. Zhang, R.Gong, M.Liang, L.Zhang等(Microbiol spectre 13:e0279124, 2025, https://doi.org/10.1128/spectrum.02791-24)将基于himar1的n-seq应用于猪链球菌,建立了一个相对密集的突变文库,结合基因组尺度的代谢建模,鉴定了244个候选必需基因。除了具有良好特征的抗生素靶点外,目前正在探索针对其他关键病原体的药物开发的几种新的候选药物,并且在经典模式生物中发现了许多以前未表征的潜在靶点。该研究强调了高通量转座子诱变和基因组尺度代谢模型在人畜共患病原体中的价值,并为未来的抗菌策略提供了重要的遗传见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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