Kaufmann Hannah, Salvador Carolina, Salazar Vinicius W, Cruz Natália, Dias Graciela Maria, Tschoeke Diogo, Campos Lucia, Sawabe Tomoo, Miyazaki Masayuki, Maruyama Fumito, Thompson Fabiano, Thompson Cristiane
Laboratory of Microbiology, Institute of Biology, UFRJ, Rio de Janeiro, Brazil.
Faculty of Medicine, Dentistry, and Health Sciences, The University of Melbourne, Melbourne, Australia.
Microb Ecol. 2025 Apr 29;88(1):36. doi: 10.1007/s00248-025-02533-0.
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.
弧菌的基因组库已得到广泛研究,尤其是在其代谢可塑性、共生相互作用以及对环境应激源的抗性机制方面。然而,对于栖息在深海海洋沉积物中的弧菌的基因组多样性和适应性却知之甚少。在本研究中,我们调查了从日本近海使用载人潜水器采集的深海岩芯沉积物中分离出的弧菌的基因组多样性。共获得50株弧菌分离株,并对其进行了表型特征鉴定以及基因组测序。在此总数中,通过检查基因组到基因组的距离、平均氨基酸同一性和表型,我们发现了22个新物种(嗜冷栖热放线菌属:1个;肠道弧菌属:1个;发光杆菌属:8个;弧菌属:12个)。这些新物种属于已知的进化枝(如费氏弧菌、肠道弧菌、深海弧菌和灿烂弧菌)以及新的进化枝(JAMM0721、JAMM0388、JAMM0395)。其余28株分离株被鉴定为已知物种:西菲嗜冷栖热放线菌(2株)、杀鲑嗜冷栖热放线菌(1株)、拜亚库肠道弧菌(1株)、挪威肠道弧菌(1株)、深海发光杆菌(3株)、狭窄发光杆菌(1株)、几丁质分解发光杆菌(1株)、嗜冷发光杆菌(1株)、印度发光杆菌(1株)、血癌发光杆菌(1株)、斯温斯发光杆菌(2株)、溶藻弧菌(3株)、鳗弧菌(1株)、坎氏弧菌(1株)、河流弧菌(1株)、巨型弧菌(1株)、迟缓弧菌(1株)、灿烂弧菌(4株)和塔斯马尼亚弧菌(1株)。基因组分析表明,所有50株弧菌都含有与高压适应相关的基因,包括传感激酶、分子伴侣、自诱导物-2(AI-2)信号传导、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周质和外膜蛋白错误折叠相关的应激反应机制。此外,还鉴定出了替代的σ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,这些基因组中抗生素抗性基因的发生率很高,其中抗生素外排泵是最丰富的一类。ugd基因在一些新物种中数量有所增加(萨摩发光杆菌新种JAMM1754:4个拷贝;幕张弧菌新种JAMM1826:3个拷贝)。该基因可能赋予这些弧菌对抗生素(多粘菌素)的抗性。