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Metatranscriptomics of the marine sponge Geodia barretti: Tackling phylogeny and function of its microbial community

机译:海洋海绵Gerdia barretti的元转录组学:解决系统发育及其微生物群落的功能

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Geodia barretti is a marine cold-water sponge harbouring high numbers of microorganisms. Significant rates of nitrification have been observed in this sponge, indicating a substantial contribution to nitrogen turnover in marine environments with high sponge cover. In order to get closer insights into the phylogeny and function of the active microbial community and the interaction with its host G. barretti, a metatranscriptomic approach was employed, using the simultaneous analysis of rRNA and mRNA. Of the 262298 RNA-tags obtained by pyrosequencing, 92% were assigned to ribosomal RNA (ribo-tags). A total of 109325 SSU rRNA ribo-tags revealed a detailed picture of the community, dominated by group SAR202 of Chloroflexi, candidate phylum Poribacteria and Acidobacteria, which was different in its composition from that obtained in clone libraries prepared form the same samples. Optimized assembly strategies allowed the reconstruction of full-length rRNA sequences from the short ribo-tags for more detailed phylogenetic studies of the dominant taxa. Cells of several phyla were visualized by FISH analyses for confirmation. Of the remaining 21325 RNA-tags, 10023 were assigned to mRNA-tags, based on similarities to genes in the databases. A wide range of putative functional gene transcripts from over 10 different phyla were identified among the bacterial mRNA-tags. The most abundant mRNAs were those encoding key metabolic enzymes of nitrification from ammonia-oxidizing archaea as well as candidate genes involved in related processes. Our analysis demonstrates the potential and limits of using a combined rRNA and mRNA approach to explore the microbial community profile, phylogenetic assignments and metabolic activities of a complex, but little explored microbial community.
机译:Geodia barretti是一种含有大量微生物的海洋冷水海绵。在这种海绵中观察到了明显的硝化速率,这表明在海绵覆盖率高的海洋环境中,氮的转化量起了很大作用。为了更深入地了解活性微生物群落的系统发育和功能以及与其宿主G. Barretti的相互作用,采用了一种转录组学方法,同时分析了rRNA和mRNA。通过焦磷酸测序获得的262298个RNA标签中,有92%被分配给了核糖体RNA(核糖标签)。共有109325个SSU rRNA核糖标签显示了该群落的详细图片,其中以绿屈挠SAR202组,候选幽门菌和嗜酸性细菌为主导,其组成与从相同样品制备的克隆文库中组成不同。优化的组装策略可从短的核糖标签重建全长rRNA序列,以对优势类群进行更详细的系统发育研究。通过FISH分析将几个门的细胞可视化以进行确认。根据与数据库中基因的相似性,在剩余的21325个RNA标签中,将10023个分配给了mRNA标签。在细菌mRNA标签中鉴定出来自10多种不同门的多种推定功能基因转录本。最丰富的mRNA是编码氨氧化古细菌硝化的关键代谢酶的mRNA,以及参与相关过程的候选基因。我们的分析表明,结合使用rRNA和mRNA的方法来探索微生物群落概况,系统发育分配和复杂但很少探索的微生物群落的代谢活性的潜力和局限性。

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