The Siphamia-Photobacterium symbiosis: a binary vertebrate model for host-microbe interactions.

IF 7.8 1区 生物学 Q1 MICROBIOLOGY
Hannah K Osland, Alison L Gould
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引用次数: 0

Abstract

SUMMARYAs microbial communities are increasingly recognized as central to animal development and health, simplified animal models have become valuable tools for exploring the complex dynamics of these interactions. The mutualism between siphonfish (Siphamia spp.) and the bioluminescent bacterium Photobacterium mandapamensis offers a naturally occurring, binary, gut-associated symbiosis within a vertebrate host that is a promising system for investigating host-microbe interactions. Over the past decade, the application of genomic, ecological, and microbiological approaches has revealed high levels of strain-level variation within this highly specific and stable symbiosis, highlighting its value for exploring host control and microbial diversity in vertebrate systems. These discoveries demonstrate the potential of the Siphamia-P. mandapamensis system as a powerful model for investigating how vertebrate hosts regulate and maintain long-term bacterial associations, particularly within gut-associated partnerships, as well as the eco-evolutionary processes that shape these relationships. This review aims to consolidate recent findings, evaluate their broader implications for vertebrate-microbe interactions, and propose future directions for research using this association as a model system.

蝇光菌共生:宿主-微生物相互作用的二元脊椎动物模型。
随着微生物群落越来越被认为是动物发育和健康的核心,简化的动物模型已成为探索这些相互作用的复杂动力学的有价值的工具。虹吸鱼(siphonfish, siphonia spp.)和生物发光细菌光杆菌(Photobacterium mandapamensis)之间的共生关系提供了一种在脊椎动物宿主内自然发生的二元肠道相关共生关系,这是研究宿主-微生物相互作用的一个有前途的系统。在过去的十年中,基因组学、生态学和微生物学方法的应用揭示了这种高度特异性和稳定的共生关系中高水平的菌株水平变化,突出了其在探索脊椎动物系统中宿主控制和微生物多样性方面的价值。这些发现证明了Siphamia-P的潜力。Mandapamensis系统是研究脊椎动物宿主如何调节和维持长期细菌联系的强大模型,特别是在肠道相关伙伴关系中,以及形成这些关系的生态进化过程。这篇综述旨在巩固最近的发现,评估它们对脊椎动物-微生物相互作用的更广泛的影响,并提出利用这种关联作为模型系统的未来研究方向。
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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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