Description of the first marine-isolated member of the under-represented phylum Gemmatimonadota, and the environmental distribution and ecogenomics of Gaopeijiales ord. nov.

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-12-17 Epub Date: 2024-11-19 DOI:10.1128/msystems.00535-24
Yu-Qi Ye, Meng-Qi Ye, Xin-Yue Zhang, You-Zhi Huang, Zi-Yang Zhou, Yan-Jun Feng, Zong-Jun Du
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Abstract

The phylum Gemmatimonadota is widespread but rarely cultured and, in fact, there are only six described species isolated from soil, freshwater, and wastewater treatment. However, no isolates of Gemmatimonadota from marine environment have been described; thus, little is known about the physiology and metabolism of members of the marine lineages. In this study, four novel facultatively anaerobic bacterial strains belonging to Gemmatimonadota were isolated from marine sediments collected from Xiaoshi Island in Weihai, China, using an aerobic enrichment method. The integrated results of phylogenetic and phenotypic characteristics supported that these four strains represent one novel species in a novel genus, for which the name Gaopeijia maritima gen. nov., sp. nov. is proposed, as the first representative of novel taxa, Gaopeijiales ord. nov., Gaopeijiaceae fam. nov. in the class Longimicrobiia. Gaopeijiales was detected in 22,884 out of 95,549 amplicon data sets, mainly from soil. However, the highest mean relative abundances were in sponge (0.7%) and marine sediment (0.35%), showing salt-related character. Most of the Gaopeijiales subgroups potentially belong to the rare bacterial biosphere. The aerobic enrichment in this study could significantly increase the relative abundance of Gaopeijiales (from 0.37% to 2.6%). Furthermore, the metabolic capabilities inferred from high-quality representative Gaopeijiales genomes/MAGs suggest that this group primarily performs chemoorganoheterotrophic metabolism with facultatively anaerobic characteristics and possesses various secondary metabolite biosynthesis gene clusters (BGCs), mirroring those observed in the four novel strains.IMPORTANCEDespite rapid advances in molecular and sequencing technologies, obtaining pure cultures remains a crucial research goal in microbiology, as it is essential for a deeper understanding of microbial metabolism. Gemmatimonadota is a widespread but rarely cultured bacterial phylum. Currently, there are only six cultured strains of this interesting group, all isolated from non-marine environments. Little is known about the physiology and metabolism of members of the marine lineages. Here we isolated and characterized four novel marine strains, and proposed a new order Gaopeijiales within Gemmatimonadota. Furthermore, the global distribution, environmental preference, and metabolic potential of Gaopeijiales are analyzed using public data. Our work enriches the resources available for the under-represented phylum Gemmatimonadota and provides insights into the physiological and metabolic characteristics of the marine lineage (Gaopeijiales) through culturology and omics.

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描述了代表性不足的门Gemmatimonadota的第一个海洋分离成员,以及Gaopeijiales ord.nov的环境分布和生态组学。
Gemmatimonadota 门广泛分布,但很少培养,事实上,仅有 6 个已描述的物种从土壤、淡水和废水处理中分离出来。然而,还没有从海洋环境中分离出 Gemmatimonadota 的描述;因此,人们对海洋生物系成员的生理和新陈代谢知之甚少。本研究采用好氧富集法,从中国威海小西岛采集的海洋沉积物中分离出四株属于 Gemmatimonadota 的新型兼性厌氧细菌。系统发育和表型特征的综合结果支持这四株菌株代表了一个新属中的一个新种,并将其命名为Gaopeijia maritima gen.在 95,549 个扩增子数据集中,有 22,884 个数据集检测到 Gaopeijiales,主要来自土壤。然而,平均相对丰度最高的是海绵(0.7%)和海洋沉积物(0.35%),显示出与盐有关的特征。大多数高培细菌亚群可能属于稀有细菌生物圈。本研究中的有氧富集可显著提高高培氏菌的相对丰度(从 0.37% 提高到 2.6%)。此外,从高质量的代表性高培氏菌基因组/MAGs 中推断出的代谢能力表明,该菌群主要进行具有兼性厌氧特征的化有机异养代谢,并拥有各种次级代谢物生物合成基因簇(BGCs),这与在四株新菌株中观察到的情况一致。真菌门(Gemmatimonadota)是一个分布广泛但很少培养的细菌门。目前,这个有趣的类群只有六株培养菌株,它们都是从非海洋环境中分离出来的。人们对海洋菌系成员的生理和新陈代谢知之甚少。在这里,我们分离并鉴定了四株新的海洋菌株,并提出了 Gemmatimonadota 内的一个新目 Gaopeijiales。此外,我们还利用公开数据分析了高培藻类的全球分布、环境偏好和代谢潜力。我们的工作丰富了代表性不足的革囊动物门的可用资源,并通过培养学和海洋学深入了解了海洋品系(Gaopeijiales)的生理和代谢特征。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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