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454 焦磷酸测序法描述微生物真核生物群落组成、多样性和相对丰度:海洋甲藻的检验。

454 pyrosequencing to describe microbial eukaryotic community composition, diversity and relative abundance: a test for marine haptophytes.

机构信息

University of Oslo, Department of Biosciences, Marine Biology, Oslo, Norway.

出版信息

PLoS One. 2013 Sep 12;8(9):e74371. doi: 10.1371/journal.pone.0074371. eCollection 2013.

Abstract

Next generation sequencing of ribosomal DNA is increasingly used to assess the diversity and structure of microbial communities. Here we test the ability of 454 pyrosequencing to detect the number of species present, and assess the relative abundance in terms of cell numbers and biomass of protists in the phylum Haptophyta. We used a mock community consisting of equal number of cells of 11 haptophyte species and compared targeting DNA and RNA/cDNA, and two different V4 SSU rDNA haptophyte-biased primer pairs. Further, we tested four different bioinformatic filtering methods to reduce errors in the resulting sequence dataset. With sequencing depth of 11000-20000 reads and targeting cDNA with Haptophyta specific primers Hap454 we detected all 11 species. A rarefaction analysis of expected number of species recovered as a function of sampling depth suggested that minimum 1400 reads were required here to recover all species in the mock community. Relative read abundance did not correlate to relative cell numbers. Although the species represented with the largest biomass was also proportionally most abundant among the reads, there was generally a weak correlation between proportional read abundance and proportional biomass of the different species, both with DNA and cDNA as template. The 454 sequencing generated considerable spurious diversity, and more with cDNA than DNA as template. With initial filtering based only on match with barcode and primer we observed 100-fold more operational taxonomic units (OTUs) at 99% similarity than the number of species present in the mock community. Filtering based on quality scores, or denoising with PyroNoise resulted in ten times more OTU99% than the number of species. Denoising with AmpliconNoise reduced the number of OTU99% to match the number of species present in the mock community. Based on our analyses, we propose a strategy to more accurately depict haptophyte diversity using 454 pyrosequencing.

摘要

下一代核糖体 DNA 测序技术越来越多地被用于评估微生物群落的多样性和结构。在这里,我们测试了 454 焦磷酸测序技术检测存在物种数量的能力,并根据细胞数量和生物量评估了甲藻门原生动物的相对丰度。我们使用由 11 种甲藻物种等数目的细胞组成的模拟群落,比较了靶向 DNA 和 RNA/cDNA 以及两种不同的 V4 SSU rDNA 甲藻偏向性引物对。此外,我们测试了四种不同的生物信息学过滤方法来减少测序数据集的错误。通过测序深度为 11000-20000 个读数并靶向 cDNA 用甲藻特异性引物 Hap454 我们检测到所有 11 个物种。根据采样深度恢复的预期物种数量的稀疏分析表明,在此模拟群落中,需要至少 1400 个读数才能恢复所有物种。相对读丰度与相对细胞数无关。尽管具有最大生物量的物种在读取中也相对丰富,但在 DNA 和 cDNA 作为模板时,不同物种的比例读丰度与比例生物量之间通常相关性较弱。454 测序产生了相当多的虚假多样性,而且以 cDNA 作为模板比 DNA 更多。基于仅基于条形码和引物匹配的初始过滤,我们在 99%相似性下观察到比模拟群落中存在的物种数量多 100 倍的操作分类单位(OTUs)。基于质量分数的过滤或用 PyroNoise 去噪导致 10 倍更多的 OTU99%比物种数量多。用 AmpliconNoise 去噪将 OTU99%的数量减少到与模拟群落中存在的物种数量相匹配。根据我们的分析,我们提出了一种使用 454 焦磷酸测序更准确地描述甲藻多样性的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/240b/3771978/6098729c697a/pone.0074371.g001.jpg

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