An optimized flow cytometry sorting-sequencing workflow reduces storage, sorting, and extraction bias in sorted microbial communities.

IF 4.1 2区 生物学 Q2 MICROBIOLOGY
Valerie Goethals, Nathan Vanwinsen, Fabian Mermans, Sofie De Gand, Nico Boon, Tom Van de Wiele, Kim De Paepe
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引用次数: 0

Abstract

Fluorescence-activated cell sorting (FACS) followed by metataxonomics is commonly used to probe the composition of microbial subpopulations with a functionality of interest. Metataxonomic analysis of sorted low-microbial-biomass samples is prone to contamination and bias introduced during sorting and DNA extraction. To improve metataxonomic accuracy, the DNA yield obtained by the DNeasy PowerSoil Pro kit was first maximized. FACS-sequencing using the optimized DNA extraction method distorted the composition of sorted microbiota by introducing sheath fluid contaminants, termed the FACSome. Since FACSome contaminants were experiment-specific, a standardized, applicable in silico decontamination method was developed to characterize and remove FACSome contamination in PacBio and Illumina metataxonomic sequencing data based on carefully selected controls. The optimized DNA extraction and decontamination methods were validated in soil, water, feces, saliva, gut reactor, and mock microbial communities. Metataxonomic profiles of non-selectively sorted and unsorted samples derived from these ecosystems did not perfectly match due to relic DNA depletion during FACS. Effective (97%) relic DNA depletion was confirmed with a spike-in experiment and is desirable since naturally present relic DNA can interfere with function-driven FACS-sequencing. A nuclease-based digest further enhanced relic DNA depletion. Since FACS depleted relic DNA, the preservation of intact cells prior to sorting is essential for activity- or viability-targeted FACS. Intact cells were best preserved during long-term -80°C storage of fecal samples that were not amended with glycerol-1× Tris-EDTA cryoprotectant.IMPORTANCEBulk meta-omics fail to provide sufficient resolution to gain mechanistic insights in microbial ecosystems. Function-driven microbiome research requires high-throughput profiling of active microbial subpopulations. These can be singled out through fluorescence-activated cell sorting (FACS) combined with function-, activity-, or viability-based labeling. The resulting low-biomass sorted samples present a currently overlooked challenge for accurate 16S rRNA gene profiling. We systematically identified all potential sources of interference to enable decontamination of 16S rRNA gene sequences from sorted microbiota. While this study focused on metataxonomic read-outs, our optimized extraction and decontamination workflow can advance other sequencing-based omics analyses of sorted microbial communities. Our optimized FACS-sequencing workflow is thus imperative to unlock the full potential of single-cell labeling and FACS, in turn enabling mode-of-action studies that will broaden our understanding of microbe-environment interactions.

优化的流式细胞术分选-测序工作流程减少了分选微生物群落的存储、分选和提取偏差。
荧光活化细胞分选(FACS)之后的元taxonomics通常用于探测微生物亚群的组成与感兴趣的功能。分类后的低微生物生物量样品的元分类学分析容易在分类和DNA提取过程中引入污染和偏差。为了提高元分类学的准确性,首先最大限度地提高dnasy PowerSoil Pro试剂盒获得的DNA产量。使用优化的DNA提取方法的facs测序通过引入鞘液污染物(称为FACSome)扭曲了已分类微生物群的组成。由于FACSome污染物是实验特异性的,因此基于精心选择的对照,开发了一种标准化的、适用于硅的去污方法来表征和去除PacBio和Illumina元分类测序数据中的FACSome污染。优化后的DNA提取和去污方法在土壤、水、粪便、唾液、肠道反应器和模拟微生物群落中进行了验证。来自这些生态系统的非选择性分选和未分选样本的元分类学特征由于FACS期间的遗物DNA枯竭而不完全匹配。有效(97%)的遗迹DNA损耗通过峰值实验得到证实,这是可取的,因为自然存在的遗迹DNA会干扰功能驱动的facs测序。基于核酸酶的消化进一步增强了遗迹DNA的消耗。由于FACS耗尽了残余DNA,因此在分选之前保存完整的细胞对于活性或活力靶向FACS至关重要。未添加甘油-1× Tris-EDTA冷冻保护剂的粪便样品在-80°C下长期保存完好的细胞。批量元组学不能提供足够的分辨率来获得微生物生态系统的机制见解。功能驱动的微生物组研究需要对活性微生物亚群进行高通量分析。这些可以通过荧光激活细胞分选(FACS)结合功能、活性或生存力标记来挑选出来。由此产生的低生物量分类样品是目前被忽视的准确16S rRNA基因分析的挑战。我们系统地鉴定了所有潜在的干扰源,以便从已分类的微生物群中去除16S rRNA基因序列。虽然这项研究主要集中在元分类学上的读数,但我们优化的提取和去污工作流程可以推进其他基于测序的微生物群落组学分析。因此,我们优化的FACS测序工作流程对于释放单细胞标记和FACS的全部潜力至关重要,从而实现作用模式研究,这将扩大我们对微生物-环境相互作用的理解。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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