耐金属环境分离株铜绿假单胞菌S-8的深入基因组和比较基因组分析。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-27 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1511507
Kiran Kumari, Ayushi Sinha, Parva Kumar Sharma, Rajnish Prakash Singh
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引用次数: 0

摘要

本研究旨在确定一种环境细菌的生存机制,这种细菌最初是从印度兰契Jhiri的废物污染土壤中分离出来的。基于16S rRNA、ANI(平均核苷酸识别)和BLAST环状图像发生器(BRIG)分析,鉴定该菌株为铜绿假单胞菌。本研究通过基因组和比较基因组分析扩展了这种细菌的特征,以了解与应激环境中生存有关的基因组特征。Illumina HiSeq平台测序结果显示,该细菌具有6.8 Mb的环状染色体,GC含量为65.9%,rna序列为63个。基因组还包含一些与植物生长促进相关的基因,如植物激素和铁载体的产生、磷酸盐的溶解、运动性和生物膜的形成等。利用在线工具进行的基因组分析揭示了属于细菌分泌系统、抗生素耐药性、毒力和外排泵等的各种基因。生物合成基因簇(BCGs)的存在表明,大量基因与非核糖体合成肽合成酶、聚酮合成酶和其他次生代谢物的产生有关。此外,菌株S-8的基因组编码多种酶,如糖苷水解酶和其他与木质纤维素分解相关的基因,表明菌株S-8具有很强的生物质降解潜力。此外,基于全基因组比较的泛基因组分析表明,核心基因组占基因库的最大部分。因此,对假单胞菌菌株进行基因组和比较基因组分析,对了解其抗金属胁迫机制、基因组进化、HGT事件等具有重要意义,为开发新分离菌株的生物技术应用开辟了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-depth genome and comparative genome analysis of a metal-resistant environmental isolate Pseudomonas aeruginosa S-8.

The present study aimed to identify the mechanisms underlying the survival of an environmental bacterium originally isolated from the waste-contaminated soil of Jhiri, Ranchi, India. Based on 16S rRNA, ANI (average nucleotide identity), and BLAST Ring Image Generator (BRIG) analysis, the isolated strain was identified as Pseudomonas aeruginosa. The present study extends the characterization of this bacterium through genomic and comparative genomic analysis to understand the genomic features pertaining to survival in stressed environments. The sequencing of the bacterium at Illumina HiSeq platform revealed that it possessed a 6.8 Mb circular chromosome with 65.9% GC content and 63 RNAs sequence. The genome also harbored several genes associated to plant growth promotion i.e. phytohormone and siderophore production, phosphate solubilization, motility, and biofilm formation, etc. The genomic analysis with online tools unraveled the various genes belonging to the bacterial secretion system, antibiotic resistance, virulence, and efflux pumps, etc. The presence of biosynthetic gene clusters (BCGs) indicated that large numbers of genes were associated to non-ribosomal synthesized peptide synthetase, polyketide synthetase, and other secondary metabolite production. Additionally, its genomes encode various CAZymes such as glycoside hydrolases and other genes associated with lignocellulose breakdown, suggesting that strain S-8 have strong biomass degradation potential. Furthermore, pan-genome analysis based on a comparison of whole genomes showed that core genome represented the largest part of the gene pools. Therefore, genome and comparative genome analysis of Pseudomonas strains is valuable for understanding the mechanism of resistance to metal stress, genome evolution, HGT events, and therefore, opens a new perspective to exploit a newly isolated bacterium for biotechnological applications.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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