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Culture-independent molecular analysis of bacterial diversity in uranium-ore/-mine waste-contaminated and non-contaminated sites from uranium mines

机译:铀矿/矿山受铀矿山污染和未污染场所细菌多样性的与文化无关的分子分析

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摘要

Soil, water and sediment samples collected from in and around Jaduguda, Bagjata and Turamdih mines were analyzed for physicochemical parameters and cultured, and yet to be cultured microbial diversity. Culturable fraction of microbial community measured as Colony Forming Unit (CFU) on R2A medium revealed microbes between 104 and 109 CFU/g sample. Community DNA was extracted from all the samples; 16S rRNA gene amplified, cloned and subject to Amplified Ribosomal DNA Restriction Analysis. Clones representing each OTU were selected and sequenced. Sequence analyses revealed that non-contaminated samples were mostly represented by Acidobacteria, Bacteroidetes, Firmicutes and Proteobacteria (β-, γ-, and/or δ-subdivisions) along with less frequent phyla Nitrospira, Deferribacteres, Chloroflexi. In contrast, samples obtained from highly contaminated samples showed distinct abundance of β-,γ- and α-Proteobacteria along with Acidobacteria,Bacteroidetes and members of Firmicutes, Chloroflexi, Candidate division, Planctomycete, Cyanobacteria and Actinobacteria as minor groups. Our data represented the baseline information on bacterial community composition within non-contaminated samples which could potentially be useful for assessing the impact of metal and radionuclides contamination due to uranium mine activities.
机译:分析了从贾杜古达,巴格亚塔和图拉米迪矿山及其周围地区采集的土壤,水和沉积物样品的理化参数,并进行了培养,尚待培养微生物多样性。在R2A培养基上以菌落形成单位(CFU)衡量的微生物群落可培养部分显示出10 4 和10 9 CFU / g样品之间的微生物。从所有样品中提取社区DNA。扩增,克隆16S rRNA基因,并对其进行了核糖体DNA限制性酶切分析。选择代表每个OTU的克隆并测序。序列分析显示,未污染的样品主要由酸杆菌,拟杆菌,硬毛菌和变形杆菌(β,γ和/或δ亚类),以及较少的门硝化螺旋体,去铁细菌,绿藻。相比之下,从高度污染的样品中获得的样品显示出丰富的β-,γ-和α-变形杆菌以及 Acidobacteria, Bacteroidetes Firmicutes,Chloroflexi成员候选部门,Planctomycete 蓝细菌放线菌是次要群体。我们的数据代表了未污染样品中细菌群落组成的基线信息,这对于评估铀矿活动对金属和放射性核素污染的影响可能很有用。

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