Systematic, high-throughput characterization of bacteriophage gene essentiality on diverse hosts

IF 20.6 1区 医学 Q1 MICROBIOLOGY
Jackie Chen, Erick D. Nilsen, Chutikarn Chitboonthavisuk, James E. Corban, Matthew Yang, Charlie Y. Mo, Srivatsan Raman
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Abstract

Understanding core and conditional gene essentiality is crucial for decoding genotype-phenotype relationships in organisms. We present phage high-throughput approach for gene essentiality mapping and profiling (PhageMaP), a high-throughput method to create genome-scale loss-of-function libraries for systematically assessing gene essentiality in bacteriophages. Using PhageMaP across diverse hosts, we generate gene essentiality maps for all or most genes in the model phages T7 and T4, as well as the non-model phage Bas63. These maps provide fundamental insights into genome organization, gene function, and host-specific conditional essentiality. By applying PhageMaP to a collection of anti-phage defense systems, we uncover phage genes that either inhibit or activate six defenses and offer mechanistic hypotheses. Furthermore, we engineer synthetic phages with enhanced infectivity by modular transfer of a PhageMaP-discovered defense inhibitor from Bas63 to T7. PhageMaP advances bacteriophage functional genomics and accelerates rational phage design for therapy.

Abstract Image

系统的,高通量的表征噬菌体基因的必要性在不同的宿主
理解核心基因和条件基因的重要性对于解码生物体的基因型-表型关系至关重要。我们提出了噬菌体基因必要性定位和分析的高通量方法(PhageMaP),这是一种高通量方法,用于创建基因组规模的功能丧失文库,用于系统地评估噬菌体中的基因必要性。利用不同宿主的PhageMaP,我们生成了模型噬菌体T7和T4以及非模型噬菌体Bas63中所有或大部分基因的基因本质图谱。这些图谱提供了对基因组组织、基因功能和宿主特异性条件必要性的基本见解。通过将PhageMaP应用于一系列抗噬菌体防御系统,我们发现了抑制或激活六种防御的噬菌体基因,并提供了机制假设。此外,通过将phagemap发现的防御抑制剂从Bas63转移到T7,我们设计了具有增强感染性的噬菌体。PhageMaP推进了噬菌体功能基因组学,加速了噬菌体治疗的合理设计。
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来源期刊
Cell host & microbe
Cell host & microbe 生物-微生物学
CiteScore
45.10
自引率
1.70%
发文量
201
审稿时长
4-8 weeks
期刊介绍: Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.
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