比较基因组学揭示了从马里亚纳海沟挑战者深渊沉积物中分离出来的哈达尔阿利碱杆菌的基因组还原和代谢潜力。

IF 4.1 2区 生物学 Q2 MICROBIOLOGY Microorganisms Pub Date : 2025-01-10 DOI:10.3390/microorganisms13010132
Shaofeng Yang, Jie Liu, Yang Liu, Weichao Wu, Jiahua Wang, Yuli Wei
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Strain Lsc_1132<sup>T</sup> contains heterogenous 16S rRNA genes, exhibiting the highest sequence similarities to the type strains of <i>Neobacillus drentensis</i> LMG 21831<sup>T</sup>, <i>Neobacillus dielmonensis</i>, <i>Neobacillus drentensis</i> NBRC 102427<sup>T</sup>, <i>Neobacillus rhizosphaerae</i>, and <i>Neobacillus soli</i> NBRC 102451<sup>T</sup>, with a range of 98.60-99.10% identity. The highest average nucleotide identity (ANI), the highest digital DNA-DNA hybridization (DDH) values, and the average amino acid identity (AAI) with <i>Neobacillus</i> sp. PS3-40 reached 73.5%, 21.4%, and 75.54%, respectively. The major cellular fatty acids of strain Lsc_1132<sup>T</sup> included iso-C<sub>15:0</sub>, Summed Feature 3 (C<sub>16:1</sub><i>ω</i>6c and/or C<sub>16:1</sub><i>ω7</i>c), iso-C<sub>17:0</sub>, anteiso-C<sub>15:0</sub>, and iso-C<sub>17:1</sub><i>ω</i>5c. The respiratory quinone of strains Lsc_1132<sup>T</sup> was MK-7. The G + C content of the genomic DNA was 40.9%. Based on the GTDB taxonomy and phenotypic data, strain Lsc_1132<sup>T</sup> could represent a novel species of a novel genus, proposed as <i>Aliineobacillus hadale</i> gen. nov. sp. nov. (type strain Lsc_1132<sup>T</sup> = MCCC 1K09620<sup>T</sup>). Metabolically, strain Lsc_1132<sup>T</sup> demonstrates a robust carbohydrate metabolism with many strain-specific sugar transporters. It also has a remarkable capacity for metabolizing amino acids and carboxylic acids. Genomic analysis reveals a streamlined genome in the organism, characterized by a significant loss of orthologous genes, including those involved in cytochrome c synthesis, aromatic compound degradation, and polyhydroxybutyrate (PHB) synthesis, which suggests its adaptation to low oxygen levels and oligotrophic conditions through alternative metabolic pathways. 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Comparative Genomics Reveals Evidence of the Genome Reduction and Metabolic Potentials of Aliineobacillus hadale Isolated from Challenger Deep Sediment of the Mariana Trench.

Hadal zones account for the deepest 45% of oceanic depth range and play an important role in ocean biogeochemical cycles. As the least-explored aquatic habitat on earth, further investigation is still required to fully elucidate the microbial taxonomy, ecological significance, metabolic diversity, and adaptation in hadal environments. In this study, a novel strain Lsc_1132T was isolated from sediment of the Mariana Trench at 10,954 m in depth. Strain Lsc_1132T contains heterogenous 16S rRNA genes, exhibiting the highest sequence similarities to the type strains of Neobacillus drentensis LMG 21831T, Neobacillus dielmonensis, Neobacillus drentensis NBRC 102427T, Neobacillus rhizosphaerae, and Neobacillus soli NBRC 102451T, with a range of 98.60-99.10% identity. The highest average nucleotide identity (ANI), the highest digital DNA-DNA hybridization (DDH) values, and the average amino acid identity (AAI) with Neobacillus sp. PS3-40 reached 73.5%, 21.4%, and 75.54%, respectively. The major cellular fatty acids of strain Lsc_1132T included iso-C15:0, Summed Feature 3 (C16:1ω6c and/or C16:1ω7c), iso-C17:0, anteiso-C15:0, and iso-C17:1ω5c. The respiratory quinone of strains Lsc_1132T was MK-7. The G + C content of the genomic DNA was 40.9%. Based on the GTDB taxonomy and phenotypic data, strain Lsc_1132T could represent a novel species of a novel genus, proposed as Aliineobacillus hadale gen. nov. sp. nov. (type strain Lsc_1132T = MCCC 1K09620T). Metabolically, strain Lsc_1132T demonstrates a robust carbohydrate metabolism with many strain-specific sugar transporters. It also has a remarkable capacity for metabolizing amino acids and carboxylic acids. Genomic analysis reveals a streamlined genome in the organism, characterized by a significant loss of orthologous genes, including those involved in cytochrome c synthesis, aromatic compound degradation, and polyhydroxybutyrate (PHB) synthesis, which suggests its adaptation to low oxygen levels and oligotrophic conditions through alternative metabolic pathways. In addition, the reduced number of paralogous genes in strain Lsc_1132T, together with its high protein-coding gene density, may further contribute to streamlining its genome and enhancing its genomic efficiency. This research expands our knowledge of hadal microorganisms and their metabolic strategies for surviving in extreme deep-sea environments.

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来源期刊
Microorganisms
Microorganisms Medicine-Microbiology (medical)
CiteScore
7.40
自引率
6.70%
发文量
2168
审稿时长
20.03 days
期刊介绍: Microorganisms (ISSN 2076-2607) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to prokaryotic and eukaryotic microorganisms, viruses and prions. It publishes reviews, research papers and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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