Picodroplet partitioned whole genome amplification of low biomass samples preserves genomic diversity for metagenomic analysis

被引:14
作者
Hammond, Maria [1 ,2 ]
Homa, Felix [1 ]
Andersson-Svahn, Helene [2 ]
Ettema, Thijs J. G. [1 ]
Joensson, Haakan N. [2 ]
机构
[1] Uppsala Univ, Dept Cell & Mol Biol, Sci Life Lab, Uppsala, Sweden
[2] Royal Inst Technol KTH, Div Prote & Nanobiotechnol, Sci Life Lab, Stockholm, Sweden
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
Whole genome amplification; Multiple displacement amplification; Metagenomics; Droplet microfluidics; Amplification bias; MULTIPLE DISPLACEMENT AMPLIFICATION; MICROBIAL COMMUNITY; IMPACT; BIAS; POLYMERASE; PHYLOGENY; INSIGHTS;
D O I
10.1186/s40168-016-0197-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Whole genome amplification (WGA) is a challenging, key step in metagenomic studies of samples containing minute amounts of DNA, such as samples from low biomass environments. It is well known that multiple displacement amplification (MDA), the most commonly used WGA method for microbial samples, skews the genomic representation in the sample. We have combined MDA with droplet microfluidics to perform the reaction in a homogeneous emulsion. Each droplet in this emulsion can be considered an individual reaction chamber, allowing partitioning of the MDA reaction into millions of parallel reactions with only one or very few template molecules per droplet. Results: As a proof-of-concept, we amplified genomic DNA from a synthetic metagenome by MDA either in one bulk reaction or in emulsion and found that after sequencing, the species distribution was better preserved and the coverage depth was more evenly distributed across the genomes when the MDA reaction had been performed in emulsion. Conclusions: Partitioning MDA reactions into millions of reactions by droplet microfluidics is a straightforward way to improve the uniformity of MDA reactions for amplifying complex samples with limited amounts of DNA.
引用
收藏
页数:8
相关论文
共 33 条
[1]   Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition [J].
Adey, Andrew ;
Morrison, Hilary G. ;
Asan ;
Xun, Xu ;
Kitzman, Jacob O. ;
Turner, Emily H. ;
Stackhouse, Bethany ;
MacKenzie, Alexandra P. ;
Caruccio, Nicholas C. ;
Zhang, Xiuqing ;
Shendure, Jay .
GENOME BIOLOGY, 2010, 11 (12)
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   Formation of dispersions using "flow focusing" in microchannels [J].
Anna, SL ;
Bontoux, N ;
Stone, HA .
APPLIED PHYSICS LETTERS, 2003, 82 (03) :364-366
[4]  
[Anonymous], ALIGNING SEQUENCE RE, DOI DOI 10.48550/ARXIV.1303.3997
[5]   Something from (almost) nothing: the impact of multiple displacement amplification on microbial ecology [J].
Binga, Erik K. ;
Lasken, Roger S. ;
Neufeld, Josh D. .
ISME JOURNAL, 2008, 2 (03) :233-241
[6]   Trimmomatic: a flexible trimmer for Illumina sequence data [J].
Bolger, Anthony M. ;
Lohse, Marc ;
Usadel, Bjoern .
BIOINFORMATICS, 2014, 30 (15) :2114-2120
[7]   Impact of library preparation protocols and template quantity on the metagenomic reconstruction of a mock microbial community [J].
Bowers, Robert M. ;
Clum, Alicia ;
Tice, Hope ;
Lim, Joanne ;
Singh, Kanwar ;
Ciobanu, Doina ;
Ngan, Chew Yee ;
Cheng, Jan-Fang ;
Tringe, Susannah G. ;
Woyke, Tanja .
BMC GENOMICS, 2015, 16
[8]   The effects of variable sample biomass on comparative metagenomics [J].
Chafee, Meghan ;
Maignien, Lois ;
Simmons, Sheri L. .
ENVIRONMENTAL MICROBIOLOGY, 2015, 17 (07) :2239-2253
[9]   Efficient de novo assembly of single-cell bacterial genomes from short-read data sets [J].
Chitsaz, Hamidreza ;
Yee-Greenbaum, Joyclyn L. ;
Tesler, Glenn ;
Lombardo, Mary-Jane ;
Dupont, Christopher L. ;
Badger, Jonathan H. ;
Novotny, Mark ;
Rusch, Douglas B. ;
Fraser, Louise J. ;
Gormley, Niall A. ;
Schulz-Trieglaff, Ole ;
Smith, Geoffrey P. ;
Evers, Dirk J. ;
Pevzner, Pavel A. ;
Lasken, Roger S. .
NATURE BIOTECHNOLOGY, 2011, 29 (10) :915-U214
[10]   Rapid amplification of plasmid and phage DNA using phi29 DNA polymerase and multiply-primed rolling circle amplification [J].
Dean, FB ;
Nelson, JR ;
Giesler, TL ;
Lasken, RS .
GENOME RESEARCH, 2001, 11 (06) :1095-1099