Genomic Repertoire of Twenty-Two Novel Vibrionaceae Species Isolated from Marine Sediments.

IF 3.3 3区 生物学 Q2 ECOLOGY
Hannah Kaufmann, Carolina Salvador, Vinicius W Salazar, Natália Cruz, Graciela Maria Dias, Diogo Tschoeke, Lucia Campos, Tomoo Sawabe, Masayuki Miyazaki, Fumito Maruyama, Fabiano Thompson, Cristiane Thompson
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引用次数: 0

Abstract

The genomic repertoire of vibrios has been extensively studied, particularly regarding their metabolic plasticity, symbiotic interactions, and resistance mechanisms to environmental stressors. However, little is known about the genomic diversity and adaptations of vibrios inhabiting deep-sea marine sediments. In this study, we investigated the genomic diversity of vibrios isolated from deep-sea core sediments collected using a manned submersible off Japan. A total of 50 vibrio isolates were obtained and characterized phenotypically, and by genome sequencing. From this total, we disclosed 22 novel species examining genome-to-genome distance, average amino acid identity, and phenotypes (Alivibrio: 1; Enterovibrio: 1; Photobacterium: 8; Vibrio: 12). The novel species have fallen within known clades (e.g., Fisheri, Enterovibrio, Profundum, and Splendidus) and novel clades (JAMM0721, JAMM0388, JAMM0395). The 28 remainder isolates were identified as known species: Aliivibrio sifiae (2), A. salmonicida (1), Enterovibrio baiacu (1), E. norvegicus (1), Photobacterium profundum (3), P. angustum (1), P. chitiniliticum (1), P. frigidiphilum (1), Photobacterium indicum (1), P. sanguinicancri (1). P. swingsii (2), Vibrio alginolyticus (3), V. anguillarum (1), V. campbellii (1), V. fluvialis (1), V. gigantis (1), V. lentus (1), V. splendidus (4), and V. tasmaniensis (1). Genomic analyses revealed that all 50 vibrios harbored genes associated with high-pressure adaptation, including sensor kinases, chaperones, autoinducer-2 (AI-2) signaling, oxidative damage repair, polyunsaturated fatty acid biosynthesis, and stress response mechanisms related to periplasmic and outer membrane protein misfolding under heat shock and osmotic stress. Additionally, alternative sigma factors, trimethylamine oxide (TMAO) respiration, and osmoprotectant acquisition pathways were identified, further supporting their ability to thrive in deep-sea environments. Notably, the genomes exhibited a high prevalence of antibiotic resistance genes, with antibiotic efflux pumps being the most abundant group. The ugd gene expanded in number in some novel species (Photobacterium satsumensis sp. nov. JAMM1754: 4 copies; Vibrio makurazakiensis sp. nov. JAMM1826: 3 copies). This gene may confer antibiotic (polymyxin) resistance to these vibrios.

海洋沉积物中22种弧菌科新物种的基因组库
弧菌的基因组库已经被广泛研究,特别是关于它们的代谢可塑性、共生相互作用和对环境胁迫的抗性机制。然而,人们对生活在深海沉积物中的弧菌的基因组多样性和适应性知之甚少。在这项研究中,我们研究了从日本近海的载人潜水器收集的深海核心沉积物中分离的弧菌的基因组多样性。共获得50株分离弧菌,并通过表型和基因组测序对其进行了表征。从这一总数中,我们发现了22个新物种,研究了基因组到基因组的距离、平均氨基酸身份和表型(Alivibrio: 1;Enterovibrio: 1;发光细菌:8;弧菌:12)。新物种属于已知分支(例如,fishi, Enterovibrio, proundum和Splendidus)和新分支(JAMM0721, JAMM0388, JAMM0395)。其余28株分离物经鉴定为已知种:猪弧菌(2株)、沙门氏菌(1株)、白肠弧菌(1株)、褐家鼠肠弧菌(1株)、深光杆菌(3株)、鳗弧菌(1株)、几丁杆菌(1株)、冷冷弧菌(1株)、indicum光杆菌(1株)、多血弧菌(1株)。swingsii弧菌(2)、褐藻溶弧菌(3)、anguillarum弧菌(1)、campbelllii弧菌(1)、fluvialis弧菌(1)、gigantis弧菌(1)、lentus弧菌(1)、spldidius弧菌(4)和tasmaniensis弧菌(1)。基因组分析显示,所有50种弧菌都含有与高压适应相关的基因,包括传感器激酶、伴侣、自诱导因子2 (AI-2)信号、氧化损伤修复、多不饱和脂肪酸生物合成,以及与热休克和渗透胁迫下质周和外膜蛋白错误折叠相关的应激反应机制。此外,还发现了其他sigma因子、氧化三甲胺(TMAO)呼吸和渗透保护剂获取途径,进一步支持了它们在深海环境中茁壮成长的能力。值得注意的是,基因组显示出抗生素抗性基因的高流行率,抗生素外排泵是最丰富的群体。ugd基因在一些新种(Photobacterium satsumensis sp. 11 . JAMM1754: 4拷贝;makurazakivibrio sp. 11 . [JAMM1826: 3拷贝]。这种基因可能赋予抗生素(多粘菌素)对这些弧菌的抗性。
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
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
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