Proteomic Analysis of Marine Bacteriophages: Structural Conservation, Post-Translational Modifications, and Phage–Host Interactions

IF 4.3 2区 生物学 Q2 MICROBIOLOGY
Shuzhen Wei, Anan Wang, Lanlan Cai, Ruijie Ma, Longfei Lu, Jiangtao Li, Rui Zhang
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Abstract

Marine bacteriophages, the most abundant biological entities in marine ecosystems, are essential in biogeochemical cycling. Despite extensive genomic data, many phage genes remain uncharacterised, creating a gap between genomic diversity and gene function knowledge. This gap limits our understanding of phage life cycles, assembly, and host interactions. In this study, we used mass spectrometry to profile the proteomes of 13 marine phages from diverse lifestyles and hosts. The analysis accurately annotated hypothetical genes, mapped virion protein arrangements, and revealed structural similarities among phages infecting the same host, particularly in tail fibre proteins. Protein structure comparisons showed conservation and variability in head and tail proteins, particularly in key domains involved in virion stabilisation and host recognition. For the first time, we identified post-translational modifications (PTMs) in marine phage proteins, which may enhance phage adaptability and help evade host immune systems. These findings suggest that phages optimise their infection strategies through structural variations and PTM modifications, improving their adaptability and host interactions.

Abstract Image

海洋噬菌体的蛋白质组学分析:结构保护、翻译后修饰和噬菌体-宿主相互作用
海洋噬菌体是海洋生态系统中最丰富的生物实体,在生物地球化学循环中起着重要作用。尽管有广泛的基因组数据,但许多噬菌体基因仍未被表征,这在基因组多样性和基因功能知识之间造成了差距。这一差距限制了我们对噬菌体生命周期、组装和宿主相互作用的理解。在这项研究中,我们使用质谱分析了来自不同生活方式和宿主的13种海洋噬菌体的蛋白质组。该分析准确地注释了假设的基因,绘制了病毒粒子蛋白排列图,并揭示了感染同一宿主的噬菌体之间的结构相似性,特别是尾部纤维蛋白。蛋白质结构比较显示头部和尾部蛋白质的保守性和可变性,特别是在涉及病毒粒子稳定和宿主识别的关键结构域。我们首次在海洋噬菌体蛋白中发现了翻译后修饰(PTMs),这可能增强噬菌体的适应性并帮助逃避宿主免疫系统。这些发现表明噬菌体通过结构变化和PTM修饰来优化其感染策略,提高其适应性和与宿主的相互作用。
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
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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