In the nodule or on the nodule? The hidden Frankia biodiversity in Casuarina nodules across continents

IF 4.8 2区 农林科学 Q1 AGRONOMY
Nadia Binte Obaid,András Patyi,Fede Berckx,Kilian Klages,Maru Bernal-Gómez,Andrea Lavello,Jesse Jentzen,Andreas Brachmann,Daniel Wibberg,Jochen Blom,Jörn Kalinowski,Sara Mehrabi,Ivan R. Kennedy,Philippe Normand,Ulrike Mathesius,Katharina Pawlowski
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Abstract

Abstract Background and Aims Actinorhizal root nodule symbioses are formed between a diverse group of mostly woody dicotyledonous plants and nitrogen-fixing soil Actinomycetota of the genus Frankia . Some of the most ecologically relevant actinorhizal plants are  Casuarina species, used widely in shelter belts and phytoremediation due to their high tolerance to abiotic stresses and ability to thrive on marginal soils. All sequenced Frankia strains isolated from Casuarina nodules using standard culture techniques show high sequence identity and belong to a single species, Frankia casuarinae . This lack of diversity in nodules is unusual in actinorhizal symbioses. We hypothesized that Casuarina nodules are colonized by Frankia strains that could not be cultivated and exhibit genome erosion. Methods To test this, we directly sequenced nodule metagenomes from four countries, followed by reconstruction of metagenome-assembled genomes (MAGs). Results Our findings show that the dominant Frankia genotypes in field samples were far more diverse than the isolated strains and included MAGs with substantial genome reduction – one having over 25% reduction compared to F. casuarinae . Notably, we observed erosion of two types of [NiFe] hydrogenases, a phenomenon linked to evolution toward obligate symbiosis in other Frankia groups. Conclusion These results indicate that potentially obligate symbionts may dominate nodules in nature but had gone undetected by conventional approaches. For applications such as reforestation or tsunami shelter belts, crushed, nodule-derived strains may offer superior ecological compatibility. We speculate that Frankia strains followed two different evolutionary trajectories; one, towards obligate symbiosis accompanied by strong genome erosion, and two, towards rhizosphere colonization involving limited genome erosion.
结节内还是结节上?木麻黄结核中隐藏的法兰克生物多样性
背景与目的放线根根瘤是一种以木本双子叶植物为主的植物群与土壤固氮放线菌群之间的共生关系。一些与生态最相关的放线根植物是木麻黄,由于其对非生物胁迫的高耐受性和在边缘土壤上茁壮成长的能力,在防护林带和植物修复中广泛使用。采用标准培养技术从木麻黄结核中分离得到的Frankia菌株均具有较高的序列一致性,属于单一种Frankia casuarinae。这种结核多样性的缺乏在放线根共生中是不寻常的。我们假设木麻黄结核是由Frankia菌株定殖的,这些菌株无法培养并表现出基因组侵蚀。为了验证这一点,我们对来自四个国家的结节宏基因组进行了直接测序,然后对宏基因组组装基因组(MAGs)进行了重建。结果田间样品中的法兰克氏菌优势基因型比分离菌株多样化得多,其中包括基因组大幅减少的mag,其中一种基因型比木麻黄氏菌减少了25%以上。值得注意的是,我们观察到两种类型的[NiFe]氢化酶的侵蚀,这一现象与其他法兰克菌群向专性共生的进化有关。结论这些结果表明,潜在的专性共生体在自然界中可能占主导地位,但传统方法无法检测到。对于诸如再造林或海啸防护带等应用,粉碎的结核衍生菌株可能具有优越的生态兼容性。我们推测Frankia菌株遵循两种不同的进化轨迹;一是专性共生,伴随着强烈的基因组侵蚀;二是根际定植,伴随着有限的基因组侵蚀。
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来源期刊
Plant and Soil
Plant and Soil 农林科学-农艺学
CiteScore
8.20
自引率
8.20%
发文量
543
审稿时长
2.5 months
期刊介绍: Plant and Soil publishes original papers and review articles exploring the interface of plant biology and soil sciences, and that enhance our mechanistic understanding of plant-soil interactions. We focus on the interface of plant biology and soil sciences, and seek those manuscripts with a strong mechanistic component which develop and test hypotheses aimed at understanding underlying mechanisms of plant-soil interactions. Manuscripts can include both fundamental and applied aspects of mineral nutrition, plant water relations, symbiotic and pathogenic plant-microbe interactions, root anatomy and morphology, soil biology, ecology, agrochemistry and agrophysics, as long as they are hypothesis-driven and enhance our mechanistic understanding. Articles including a major molecular or modelling component also fall within the scope of the journal. All contributions appear in the English language, with consistent spelling, using either American or British English.
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