通过细胞外DNA解码自然和人为干扰事件诱导的过去微生物群落变化。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
S Varrella, M Tangherlini, C Corinaldesi, L Musco, A Schirone, G Armiento, R Danovaro, A Dell'Anno
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引用次数: 0

摘要

沿海海洋生态系统面临着包括工业污染物排放在内的多种人为压力源不断升级的威胁。尽管几十年来的工业活动影响着海洋生态系统,但对微生物群落和相关关键生态功能的长期影响尚不清楚。在这里,我们分析了保存在沉积物层中的细胞外DNA的原核遗传特征,这些沉积物层可追溯到17世纪中叶至今,收集自污染最严重的欧洲沿海地区之一(即第勒尼安海的Bagnoli-Coroglio湾)的两个地点,那里的工业活动始于20世纪初,结束于1992年。古细菌16S rDNA拷贝数高于细菌,在工业前火山期和工业发展激烈期分别达到2.3 × 107拷贝和8.8 × 107拷贝。沿沉积物垂直剖面确定的古细菌遗传特征大部分属于深海古菌。与工业化时期(182个家族)相比,工业化前时期70个原核生物扩增子序列变异(asv)的多样性较低,这表明原核生物有能力响应和改变随时间变化的环境条件。微生物β多样性值较高,两个岩心中有50多个原核生物类群发生了重大变化,表明化学污染和火山爆发促进了微生物演替,选择了更适应这种不利生态条件的某些类群。我们的研究结果表明,海洋沉积物的细胞外DNA库可以保存底栖微生物多样性长期变化的信息,是了解生态系统动态的宝贵档案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decoding Past Microbial Communities Shifts Induced by Natural and Anthropogenic Disturbance Events Through Extracellular DNA.

Coastal marine ecosystems face escalating threats from multiple anthropogenic stressors, including the release of industrial contaminants. Despite decades of industrial activity impacting marine ecosystems, long-term effects on microbial communities and related key ecological functions remain unclear. Here, we analysed the prokaryotic genetic signatures of extracellular DNA preserved in sediment layers dating from the mid-17th century to the present day collected from two sites of one of the most polluted European coastal areas (i.e., Bagnoli-Coroglio Bay, Tyrrhenian Sea), where industrial activities began in the early 20th century and ended in 1992. Archaeal 16S rDNA copy numbers were higher than bacterial ones, reaching values of 2.3 and 8.8 × 107 copies during pre-industrial volcanic episodes and the intense industrial development period, respectively. Most of the archaeal genetic signatures identified along the sediment vertical profiles belong to Bathyarchaeia. The pre-industrial period showed lower diversity in terms of Amplicon Sequence Variants (ASVs) belonging to 70 prokaryotic families when compared with industrialisation periods (182 families), suggesting prokaryotic ability to respond and change in relation to modified environmental conditions occurring over time. High microbial β-diversity values were observed, with major shifts occurring for more than 50 prokaryotic taxa in both cores, suggesting that chemical contamination and volcanic eruptions fostered microbial succession, selecting certain taxa more adapted to cope with such adverse ecological conditions. Our findings indicate that extracellular DNA pools of marine sediments can hold information on long-term changes in benthic microbial diversity, representing valuable archives for understanding ecosystem dynamics over time.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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