两种携带军团菌共生菌的未栽培奈格莱氏菌的比较单细胞基因组学。

IF 3.1 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-09-30 Epub Date: 2025-08-27 DOI:10.1128/msphere.00352-25
Jamie McGowan, Estelle S Kilias, James Lipscombe, Elisabet Alacid, Tom Barker, Leah Catchpole, Seanna McTaggart, Sally D Warring, Karim Gharbi, Thomas A Richards, Neil Hall, David Swarbreck
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引用次数: 0

摘要

鞭毛虫属的变形虫是自由生活的原生生物,在世界各地的土壤和淡水栖息地中无处不在。它们包括“食脑阿米巴”福氏奈格里原虫,这是一种机会性病原体,可引起原发性阿米巴脑膜脑炎,这是一种罕见但致命的人类感染。除了它们的直接致病性,原生生物还可以作为细胞内细菌病原体的环境储存库,如军团菌,在环境中持续存在和繁殖。在这项研究中,我们对从英国利姆河分离的两种未栽培的Naegleria进行了单细胞基因组测序。从单个细胞中,我们产生了两个高度完整的奈格莱氏菌基因组。系统发育分析表明这些物种是富氏耐格丽蝇和pagei耐格丽蝇的近亲。研究纳格里氏菌进化基因组学,我们确定了编码抗stasin样结构域的基因家族,这些结构域被认为是抑制吸血水蛭凝血的因素。抗stasin-like结构域在所有测序的Naegleria物种及其近亲Willaertia magna中都被鉴定出来,但在其他方面主要局限于动物基因组。值得注意的是,我们从每个Naegleria单细胞样本中恢复了高度完整的细菌基因组。系统基因组分析显示,这两种细菌都属于军团菌科。两种细菌的基因组都编码了一整套的分泌系统和效应库。我们从植物致病性黄单胞菌(Xanthomonas sp .)中鉴定出推测的军团菌效应物,它们在蛋白质序列和预测结构方面与TAL (Transcription activator-like)效应物相似,代表了一种潜在的新型军团菌效应物。我们的研究强调了单细胞环境基因组学方法的优势,它使细胞内病原体与其宿主的直接关联能够更好地理解宿主-病原体相互作用的进化。重要性除了它们的直接致病潜力外,环境中发现的变形虫和其他原生生物还可以作为细胞内细菌病原体在环境中持续存在、进化和繁殖的宿主,间接威胁人类健康。尽管它们很重要,但人们对原生生物与细菌的相互作用仍然知之甚少。在这项研究中,我们采用单细胞基因组学方法对两种未培养的阿米巴奈格莱虫进行了基因组测序,这两种细菌都含有新型军团菌。从单个细胞中,我们恢复了高度完整的真核生物和细菌共生体基因组组装。我们的工作证明了单细胞测序方法在将细胞内病原体与其宿主直接联系起来方面的力量,可以更好地理解原生生物与细菌相互作用的进化,以及原生生物在促进细菌病原体在环境中长期存在方面所起的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative single-cell genomics of two uncultivated Naegleria species harboring Legionella cobionts.

Amoeboflagellates of the genus Naegleria are free-living protists ubiquitously found in soil and freshwater habitats worldwide. They include the "brain-eating amoeba" Naegleria fowleri, an opportunistic pathogen that causes primary amoebic meningoencephalitis, a rare but fatal infection of humans. Beyond their direct pathogenicity, protists can also act as environmental reservoirs for intracellular bacterial pathogens, such as Legionella spp., to persist and multiply in the environment. In this study, we carried out single-cell genome sequencing of two uncultivated Naegleria species isolated from the River Leam in England. From single cells, we generated two highly complete Naegleria genomes. Phylogenetic analyses placed these species as close relatives of Naegleria fultoni and Naegleria pagei. Exploring Naegleria evolutionary genomics, we identified gene families encoding antistasin-like domains, which have been characterized as factors that inhibit coagulation in blood-feeding leeches. Antistasin-like domains were identified in all sequenced Naegleria species and their close relative Willaertia magna, yet are otherwise largely restricted to animal genomes. Significantly, we recovered highly complete bacterial genomes from each Naegleria single-cell sample. Phylogenomic analysis revealed that both bacteria belong to the Legionellaceae family. Both bacterial genomes encode comprehensive sets of secretion systems and effector arsenals. We identified putative Legionella effectors that resemble TAL (Transcription activator-like) effectors from plant pathogenic Xanthomonas spp. in terms of protein sequence and predicted structure, representing a potentially novel class of Legionella effectors. Our study highlights the advantages of single-cell environmental genomics approaches, which enable direct association of intracellular pathogens with their hosts to better understand the evolution of host-pathogen interactions.IMPORTANCEBeyond their direct pathogenic potential, amoebae and other protists found in the environment can indirectly threaten human health by serving as reservoirs for intracellular bacterial pathogens to persist, evolve, and multiply in the environment. Despite their importance, protist-bacterial interactions remain poorly understood. In this study, we employed single-cell genomics to sequence the genomes of two uncultivated Naegleria amoebae, both harboring novel Legionella bacteria. From individual cells, we recovered highly complete eukaryotic and bacterial cobiont genome assemblies. Our work demonstrates the power of single-cell sequencing approaches in directly linking intracellular pathogens to their hosts to better understand the evolution of protist-bacterial interactions and the role that protists play in facilitating bacterial pathogens to persist long term in the environment.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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