Dyella aluminiiresistens sp. nov., a Al3+-tolerant bacterium with the ability to inhibit Fusarium oxysporum f. sp. melonis isolated from rhizosphere soil of muskmelon.

IF 2 3区 生物学 Q4 MICROBIOLOGY International journal of systematic and evolutionary microbiology Pub Date : 2025-01-01 DOI:10.1099/ijsem.0.006611
Yi Li, Jiaojiao Wang, Chunyuan Wu, Jian He, Qinfen Li, Xiao Deng, Huadong Tan
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Abstract

A bacterial strain, designated as A6T, was isolated from the rhizosphere soil of a healthy muskmelon in Wenchang, Hainan Province, China. The cells of strain A6T were Gram-negative, aerobic, short rod and motile with a single polar flagellum. Strain A6T could tolerate up to 55.0 mM Al3+ and inhibited the growth of Fusarium oxysporum f. sp. melonis, which is the pathogen of muskmelon Fusarium wilt. Growth occurred at 15-37 ℃ (optimum at 30 ℃), pH 4.5-8.0 (optimum pH 6.5) and with 0-3.0 % NaCl (w/v; optimum, 0.5%). Strain A6T shared the highest 16S rRNA gene sequence similarities with Dyella lutea SaT (98.0%), followed by Dyella thiooxydans ATSB10T (98.0%), Frateuria edaphi 5GH9-34T (97.9%), Dyella nitratireducens DHG59T (97.7%), Frateuria defendens DHoT (97.7%) and Frateuria soli 5GH9-11T (97.7%). Phylogenetic trees based on 16S rRNA gene and genomic sequences indicated that strain A6T belonged to the genus Dyella and formed a subclade with Dyella lutea SaT and Dyella thiooxydans ATSB10T. The average nucleotide identity (ANI), average amino acid identity (AAI) and digital DNA-DNA hybridization (dDDH) values between A6T and its closely related type strains were 78.8-80.8 %, 70.0-71.7 % and 20.5-22.1 %, respectively. The sole respiratory quinone was ubiquinone-8 (Q-8). The polar lipid profile consisted of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylethanolamine (PE), two unidentified aminophospholipids (APL1-2) and three unidentified phospholipids (PL1-3). The major cellular fatty acids (≥5 %) were iso-C17 : 0, C16 : 0, summed feature 9 (iso-C17 : 1ω9c and/or C16 : 0 10-methyl), iso-C15 : 0, iso-C16 : 0 and anteiso-C17 : 0. The genome size of strain A6T was 3.7 Mb with a DNA G+C content of 65.1%. Based on the phenotypic, phylogenetic, genotypic and chemotaxonomic features, strain A6T represents a novel species in the genus Dyella, for which Dyella aluminiiresistens A6T sp. nov. is proposed. The type strain is A6T (= GDMCC 1.4640T = KCTC 92542T).

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从甜瓜根际土壤中分离出的耐Al3+的耐铝迪氏菌,具有抑制甜瓜尖孢镰刀菌的能力。
从海南文昌健康甜瓜根际土壤中分离到一株A6T菌株。菌株A6T为革兰氏阴性,需氧型,短杆型,单极鞭毛可运动。菌株A6T能耐受高达55.0 mM的Al3+,并能抑制甜瓜枯萎病病原菌甜瓜尖孢镰刀菌的生长。15 ~ 37℃(30℃最适)、pH 4.5 ~ 8.0 (pH 6.5最适)和0 ~ 3.0 % NaCl (w/v;最佳,0.5%)。菌株A6T的16S rRNA基因序列相似性最高(98.0%),其次是硫代氧化Dyella ATSB10T(98.0%)、edaphifrateuria 5GH9-34T(97.9%)、硝化还原Dyella DHG59T(97.7%)、防御Frateuria DHoT(97.7%)和固体Frateuria 5GH9-11T(97.7%)。基于16S rRNA基因和基因组序列的系统进化树表明,A6T菌株属于痢疾菌属,与黄氏痢疾菌SaT和硫氧氧化痢疾菌ATSB10T形成一个亚枝。A6T与近缘型菌株的平均核苷酸同源性(ANI)、平均氨基酸同源性(AAI)和数字DNA-DNA杂交(dDDH)值分别为78.8 ~ 80.8%、70.0 ~ 71.7%和20.5 ~ 22.1%。唯一的呼吸醌为泛醌-8 (Q-8)。极性脂质谱由二磷脂酰甘油(DPG)、磷脂酰甘油(PG)、磷脂酰乙醇胺(PE)、2种未识别的氨基磷脂(APL1-2)和3种未识别的磷脂(PL1-3)组成。主要细胞脂肪酸(≥5%)为iso-C17: 0, C16: 0,特征9 (iso-C17: 1 ω9c和/或C16: 0 10-甲基),iso-C15: 0, iso-C16: 0和前iso-C17: 0。菌株A6T的基因组大小为3.7 Mb, DNA G+C含量为65.1%。基于表型、系统发育、基因型和化学分类特征,菌株A6T代表了Dyella属的一个新种,该菌株被认为是Dyella aluminiiresistens A6T sp. 11。型应变为A6T (= GDMCC 1.4640T = KCTC 92542T)。
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来源期刊
CiteScore
5.20
自引率
21.40%
发文量
426
审稿时长
1 months
期刊介绍: Published by the Microbiology Society and owned by the International Committee on Systematics of Prokaryotes (ICSP), a committee of the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, International Journal of Systematic and Evolutionary Microbiology is the leading forum for the publication of novel microbial taxa and the ICSP’s official journal of record for prokaryotic names. The journal welcomes high-quality research on all aspects of microbial evolution, phylogenetics and systematics, encouraging submissions on all prokaryotes, yeasts, microfungi, protozoa and microalgae across the full breadth of systematics including: Identification, characterisation and culture preservation Microbial evolution and biodiversity Molecular environmental work with strong taxonomic or evolutionary content Nomenclature Taxonomy and phylogenetics.
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