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评估噬菌体裂解活性:从噬菌斑测定到单细胞技术。

Evaluating phage lytic activity: from plaque assays to single-cell technologies.

作者信息

Panteleev Vladimir, Kulbachinskiy Andrey, Gelfenbein Daria

机构信息

Laboratory of Antimicrobial Agents, Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.

Laboratory of Prokaryotic Immune Systems, Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.

出版信息

Front Microbiol. 2025 Aug 29;16:1659093. doi: 10.3389/fmicb.2025.1659093. eCollection 2025.

DOI:10.3389/fmicb.2025.1659093
PMID:40950580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12427128/
Abstract

Bacteriophages are the most abundant biological entities on Earth, playing critical roles in microbial ecology, evolution, and horizontal gene transfer. Since the discovery of bacteriophages in the early 20th century, a wide range of techniques has been developed to study their lytic activity. This review provides a perspective on the wide range of methods for studying phage-bacteria interactions, spanning classical bulk-culture techniques and modern single-cell and high-throughput approaches. The first section covers solid culture methods relying on plaque formation phenomenon, which allow for quantification of infectious viruses, phage host-range establishment, and analysis of certain phage traits, now augmented by robotic high-throughput screening. The second section focuses on liquid culture approaches, utilizing optical density measurements, quantitative PCR, metabolic assays and cell damage assays to measure the infection dynamics. The third section details single-cell techniques, which help to dissect the heterogeneity of infection within cell populations, using microscopy, microfluidics, next-generation sequencing, and Hi-C methods. The integration of these diverse methods has greatly advanced our understanding of the molecular mechanisms of phage infection, bacterial immunity, and facilitated phage therapy development. This review is dedicated to the 110th anniversary of phage discovery and is aimed to guide researchers in selecting optimal techniques in the fast-growing field of phage biology, phage-host interactions, bacterial immunity, and phage therapy.

摘要

噬菌体是地球上数量最多的生物实体,在微生物生态学、进化和水平基因转移中发挥着关键作用。自20世纪初发现噬菌体以来,已开发出多种技术来研究其裂解活性。本综述提供了关于研究噬菌体 - 细菌相互作用的广泛方法的观点,涵盖经典的批量培养技术以及现代的单细胞和高通量方法。第一部分介绍了基于噬菌斑形成现象的固体培养方法,该方法可用于定量感染性病毒、确定噬菌体宿主范围以及分析某些噬菌体特性,现在通过机器人高通量筛选得到了增强。第二部分重点介绍液体培养方法,利用光密度测量、定量PCR、代谢测定和细胞损伤测定来测量感染动态。第三部分详细介绍单细胞技术,该技术使用显微镜、微流控技术、下一代测序和Hi-C方法,有助于剖析细胞群体内感染的异质性。这些不同方法的整合极大地推进了我们对噬菌体感染、细菌免疫的分子机制的理解,并促进了噬菌体疗法的发展。本综述是为了纪念噬菌体发现110周年而作,旨在指导研究人员在噬菌体生物学、噬菌体 - 宿主相互作用、细菌免疫和噬菌体疗法等快速发展的领域中选择最佳技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/6e80588a3750/fmicb-16-1659093-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/fd7aee0ba790/fmicb-16-1659093-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/479c88bc6b98/fmicb-16-1659093-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/b6f471469530/fmicb-16-1659093-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/6e80588a3750/fmicb-16-1659093-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/fd7aee0ba790/fmicb-16-1659093-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/479c88bc6b98/fmicb-16-1659093-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/b6f471469530/fmicb-16-1659093-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d73/12427128/6e80588a3750/fmicb-16-1659093-g004.jpg

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Programming CRISPRi to control the lifecycle of bacteriophage T7.对CRISPRi进行编程以控制噬菌体T7的生命周期。
Front Microbiol. 2025 Feb 12;16:1497650. doi: 10.3389/fmicb.2025.1497650. eCollection 2025.
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CRISPRi-ART enables functional genomics of diverse bacteriophages using RNA-binding dCas13d.CRISPRi-ART技术利用RNA结合型dCas13d实现了多种噬菌体的功能基因组学研究。
Nat Microbiol. 2025 Mar;10(3):694-709. doi: 10.1038/s41564-025-01935-7. Epub 2025 Feb 26.
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Prediction of strain level phage-host interactions across the Escherichia genus using only genomic information.仅使用基因组信息预测整个大肠埃希氏菌属中噬菌体-宿主相互作用的应变水平。
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