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你是我的宿主吗?用于将噬菌体与宿主联系起来的方法概述。

Are You My Host? An Overview of Methods Used to Link Bacteriophages with Hosts.

作者信息

Hyman Paul

机构信息

Department of Biology and Toxicology, Ashland University, Ashland, OH 44805, USA.

出版信息

Viruses. 2025 Jan 5;17(1):65. doi: 10.3390/v17010065.

Abstract

Until recently, the only methods for finding out if a particular strain or species of bacteria could be a host for a particular bacteriophage was to see if the bacteriophage could infect that bacterium and kill it, releasing progeny phages. Establishing the host range of a bacteriophage thus meant infecting many different bacteria and seeing if the phage could kill each one. Detection of bacterial killing can be achieved on solid media (plaques, spots) or broth (culture clearing). More recently, additional methods to link phages and hosts have been developed. These include methods to show phage genome entry into host cells (e.g., PhageFISH); proximity of phage and host genomes (e.g., proximity ligation, polonies, viral tagging); and analysis of genomes and metagenomes (e.g., CRISPR spacer analysis, metagenomic co-occurrence). These methods have advantages and disadvantages. They also are not measuring the same interactions. Host range can be divided into multiple host ranges, each defined by how far the phage can progress in the infection cycle. For example, the ability to effect genome entry (penetrative host range) is different than the ability to produce progeny (productive host range). These different host ranges reflect bacterial defense mechanisms that block phage growth and development at various stages in the infection cycle. Here, I present a comparison of the various methods used to identify bacteriophage-host relationships with a focus on what type of host range is being measured or predicted.

摘要

直到最近,确定某一特定菌株或细菌物种是否可能是特定噬菌体宿主的唯一方法,是看该噬菌体是否能感染并杀死那种细菌,释放出子代噬菌体。因此,确定噬菌体的宿主范围意味着要感染许多不同的细菌,看噬菌体是否能杀死每一种细菌。细菌杀伤的检测可以在固体培养基(噬菌斑、斑点)或肉汤(培养物澄清)中实现。最近,已开发出其他将噬菌体与宿主联系起来的方法。这些方法包括显示噬菌体基因组进入宿主细胞的方法(例如,噬菌体荧光原位杂交);噬菌体和宿主基因组的接近程度(例如,邻近连接、聚合酶克隆、病毒标记);以及基因组和宏基因组分析(例如,CRISPR间隔区分析、宏基因组共现分析)。这些方法各有优缺点。它们测量的也不是相同的相互作用。宿主范围可以分为多个宿主范围,每个宿主范围由噬菌体在感染周期中能够进展的程度来定义。例如,影响基因组进入的能力(穿透性宿主范围)与产生子代的能力(生产性宿主范围)是不同的。这些不同的宿主范围反映了在感染周期的各个阶段阻止噬菌体生长和发育的细菌防御机制。在这里,我对用于鉴定噬菌体-宿主关系的各种方法进行比较,重点是所测量或预测的宿主范围类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c56/11769497/479329eacd86/viruses-17-00065-g001.jpg

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