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利用分子条形码和全基因组测序探索木薯根际枯草芽孢杆菌分离株的遗传多样性和基因组见解。

Exploring genetic diversity and genomic insights of Bacillus subtilis isolates from cassava rhizosphere using molecular barcoding and whole genome sequencing.

作者信息

Sraphet Supajit, Javadi Bagher

机构信息

Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom, 73170, Thailand.

Department of Sciences, Faculty of Science and Technology, Suan Sunandha Rajabhat University, Bangkok, 10300, Thailand.

出版信息

Sci Rep. 2025 Jul 2;15(1):22708. doi: 10.1038/s41598-025-08736-2.

Abstract

Bacillus subtilis plays a significant role in both agriculture and industry. It is commonly isolated from agricultural environments, particularly various soil types. This study aimed to investigate DNA barcoding and whole-genome sequencing of B. subtilis strains, focusing on those specific to the cassava rhizosphere. Genetic identification and diversity of B. subtilis strains isolated from the rhizosphere of the Piroon 2 cassava cultivar were initially characterized using 16 S rDNA, a molecular marker for species-level identification. To explore strain-specific biodiversity within B. subtilis, repetitive DNA elements-specifically extragenic palindromic and BOX sequences-were analyzed across the genomes of the isolated strains. These repetitive sequences revealed two main structural patterns, providing clear and distinct genomic fingerprints for biodiversity analysis. The results showed that both REP and BOX sequences were highly conserved within specific regions of the B. subtilis genome, resulting in reliable and reproducible DNA patterns suitable for whole-genome phylogenetic analysis. While the 16 S rDNA approach showed a high sequence similarity among the B. subtilis strains (99.98%), whole-genome analysis using repetitive sequences allowed for clearer differentiation, with phylogenetic distances exceeding 97%. Whole-genome sequencing of the elite strain BsPr8 was performed using the Illumina MiSeq platform. The sequencing results yielded 56 contigs, with an average GC content of 43.67% and a total genome size of approximately 4,050 Kbp. Genome annotation identified 3,575 proteins with functional assignments, including 1,055 enzymes classified by Enzyme Commission numbers. The PATRIC database further annotated 3,937 genus-specific protein families. Additionally, 45 genes homologous to known antibiotic resistance genes were identified within the BsPr8 genome. These findings have important implications for sustainable agricultural practices and cassava cultivation. By elucidating the genetic diversity and genomic characteristics of B. subtilis strains, this study facilitates the identification of beneficial traits-such as plant growth promotion, pathogen suppression, and improved nutrient uptake. These strains hold potential for development as biofertilizers or biopesticides, offering an environmentally friendly alternative to conventional chemical inputs.

摘要

枯草芽孢杆菌在农业和工业中都发挥着重要作用。它通常从农业环境中分离得到,尤其是各种土壤类型。本研究旨在调查枯草芽孢杆菌菌株的DNA条形码和全基因组测序,重点关注木薯根际特有的菌株。最初使用16S rDNA(一种用于物种水平鉴定的分子标记)对从皮伦2号木薯品种根际分离的枯草芽孢杆菌菌株进行遗传鉴定和多样性分析。为了探索枯草芽孢杆菌内菌株特异性的生物多样性,对分离菌株的基因组分析了重复DNA元件,特别是基因外回文序列和BOX序列。这些重复序列揭示了两种主要的结构模式,为生物多样性分析提供了清晰且独特的基因组指纹。结果表明,REP和BOX序列在枯草芽孢杆菌基因组的特定区域内高度保守,产生了适用于全基因组系统发育分析的可靠且可重复的DNA模式。虽然16S rDNA方法显示枯草芽孢杆菌菌株之间的序列相似性很高(99.98%),但使用重复序列的全基因组分析能够实现更清晰的区分,系统发育距离超过97%。使用Illumina MiSeq平台对优良菌株BsPr8进行了全基因组测序。测序结果产生了56个重叠群,平均GC含量为43.67%,总基因组大小约为4050 Kbp。基因组注释鉴定出3575个具有功能注释的蛋白质,其中包括1055个按酶委员会编号分类的酶。PATRIC数据库进一步注释了3937个属特异性蛋白质家族。此外,在BsPr8基因组中鉴定出45个与已知抗生素抗性基因同源的基因。这些发现对可持续农业实践和木薯种植具有重要意义。通过阐明枯草芽孢杆菌菌株的遗传多样性和基因组特征,本研究有助于识别有益特性,如促进植物生长、抑制病原体和改善养分吸收。这些菌株具有开发为生物肥料或生物农药的潜力,为传统化学投入提供了一种环境友好的替代方案。

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