Ospino Melody Cabrera, Engel Katja, Ruiz-Navas Santiago, Binns W Jeffrey, Doxey Andrew C, Neufeld Josh D
Department of Biology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.
Safety and Technical Research, Nuclear Waste Management Organization of Canada, Toronto, Ontario M4T 2S3, Canada.
ISME Commun. 2024 Feb 12;4(1):ycae024. doi: 10.1093/ismeco/ycae024. eCollection 2024 Jan.
Combining multiple displacement amplification (MDA) with metagenomics enables the analysis of samples with extremely low DNA concentrations, making them suitable for high-throughput sequencing. Although amplification bias and nonspecific amplification have been reported from MDA-amplified samples, the impact of MDA on metagenomic datasets is not well understood. We compared three MDA methods (i.e. bulk MDA, emulsion MDA, and primase MDA) for metagenomic analysis of two DNA template concentrations (approx. 1 and 100 pg) derived from a microbial community standard "mock community" and two low biomass environmental samples (i.e. borehole fluid and groundwater). We assessed the impact of MDA on metagenome-based community composition, assembly quality, functional profiles, and binning. We found amplification bias against high GC content genomes but relatively low nonspecific amplification such as chimeras, artifacts, or contamination for all MDA methods. We observed MDA-associated representational bias for microbial community profiles, especially for low-input DNA and with the primase MDA method. Nevertheless, similar taxa were represented in MDA-amplified libraries to those of unamplified samples. The MDA libraries were highly fragmented, but similar functional profiles to the unamplified libraries were obtained for bulk MDA and emulsion MDA at higher DNA input and across these MDA libraries for the groundwater sample. Medium to low-quality bins were possible for the high input bulk MDA metagenomes for the most simple microbial communities, borehole fluid, and mock community. Although MDA-based amplification should be avoided, it can still reveal meaningful taxonomic and functional information from samples with extremely low DNA concentration where direct metagenomics is otherwise impossible.
将多重置换扩增(MDA)与宏基因组学相结合,能够对DNA浓度极低的样本进行分析,使其适用于高通量测序。尽管已有报道称MDA扩增的样本存在扩增偏差和非特异性扩增,但MDA对宏基因组数据集的影响尚未得到充分了解。我们比较了三种MDA方法(即整体MDA、乳液MDA和引发酶MDA),用于对来自微生物群落标准“模拟群落”的两种DNA模板浓度(约1和100 pg)以及两种低生物量环境样本(即钻孔液和地下水)进行宏基因组分析。我们评估了MDA对基于宏基因组的群落组成、组装质量、功能概况和分箱的影响。我们发现所有MDA方法都存在针对高GC含量基因组的扩增偏差,但诸如嵌合体、假象或污染等非特异性扩增相对较低。我们观察到MDA相关的微生物群落概况代表性偏差,特别是对于低输入DNA以及使用引发酶MDA方法时。然而,MDA扩增文库中呈现的分类单元与未扩增样本中的相似。MDA文库高度碎片化,但对于整体MDA和乳液MDA,在较高DNA输入时以及针对地下水样本的这些MDA文库中,获得了与未扩增文库相似的功能概况。对于最简单的微生物群落、钻孔液和模拟群落,高输入整体MDA宏基因组可以进行中等至低质量的分箱。尽管应避免基于MDA的扩增,但它仍能从DNA浓度极低的样本中揭示有意义的分类学和功能信息,而直接进行宏基因组学分析在其他情况下是不可能的。