Capturing and cultivating single bacterial cells in gel microdroplets to obtain near-complete genomes

被引:32
作者
Dichosa, Armand E. K. [1 ]
Daughton, Ashlynn R. [1 ]
Reitenga, Krista G. [1 ]
Fitzsimons, Michael S. [1 ]
Han, Cliff S. [1 ]
机构
[1] Los Alamos Natl Lab, Genome Sci Programs, Bioenergy & Biome Sci B 11, Los Alamos, NM 87544 USA
关键词
FLOW-CYTOMETRY; AMPLIFICATION; MICROORGANISMS; ENUMERATION; PHYLOGENY; SEQUENCES; INSIGHTS; SAMPLES;
D O I
10.1038/nprot.2014.034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Assembling a complete genome from a single bacterial cell, termed single-cell genomics, is challenging with current technologies. Recovery rates of complete genomes from fragmented assemblies of single-cell templates significantly vary. Although increasing the amount of genomic template material by standard cultivation improves recovery, most bacteria are unfortunately not amenable to traditional cultivation, possibly owing to the lack of unidentified, yet necessary, growth signals and/ or specific symbiotic influences. To overcome this limitation, we adopted and modified the method of cocultivation of single-captured bacterial cells in gel microdroplets (GMDs) to improve full genomic sequence recovery. By completing multiple genomes of two novel species derived from single cells, we demonstrated its efficacy on diverse bacterial species using human oral and gut microbiome samples. Here we describe a detailed protocol for capturing single bacterial cells, cocultivating them in medium and isolating microcolonies in GMDs with flow cytometry. Beginning with preliminary studies, obtaining GMDs with single microcolonies for whole-genome amplification may take similar to 4 weeks.
引用
收藏
页码:608 / 621
页数:14
相关论文
共 37 条
[1]   16 S rDNA primers and the unbiased assessment of thermophile diversity [J].
Baker, GC ;
Cowan, DA .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2004, 32 :218-221
[2]   Decreasing amplification bias associated with multiple displacement amplification and short tandem repeat genotyping [J].
Ballantyne, Kaye N. ;
van Oorschot, Roland A. H. ;
Muharam, Iman ;
van Daal, Angela ;
Mitchell, R. John .
ANALYTICAL BIOCHEMISTRY, 2007, 368 (02) :222-229
[3]   Assessment and interpretation of bacterial viability by using the LIVE/DEAD BacLight kit in combination with flow cytometry [J].
Berney, Michael ;
Hammes, Frederik ;
Bosshard, Franziska ;
Weilenmann, Hans-Ulrich ;
Egli, Thomas .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (10) :3283-3290
[4]   Digital MDA for enumeration of total nucleic acid contamination [J].
Blainey, Paul C. ;
Quake, Stephen R. .
NUCLEIC ACIDS RESEARCH, 2011, 39 (04) :e19
[5]  
Borth N, 2000, BIOTECHNOL BIOENG, V71, P266, DOI 10.1002/1097-0290(2000)71:4<266::AID-BIT1016>3.0.CO
[6]  
2-2
[7]   TREPONEMA-PALLIDUM IN GEL MICRODROPLETS - A NOVEL STRATEGY FOR INVESTIGATION OF TREPONEMAL MOLECULAR ARCHITECTURE [J].
COX, DL ;
AKINS, DR ;
PORCELLA, SF ;
NORGARD, MV ;
RADOLF, JD .
MOLECULAR MICROBIOLOGY, 1995, 15 (06) :1151-1164
[8]   Limited surface exposure of Borrelia burgdorferi outer surface lipoproteins [J].
Cox, DL ;
Akins, DR ;
Bourell, KW ;
Lahdenne, P ;
Norgard, MV ;
Radolf, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7973-7978
[9]   Artificial Polyploidy Improves Bacterial Single Cell Genome Recovery [J].
Dichosa, Armand E. K. ;
Fitzsimons, Michael S. ;
Lo, Chien-Chi ;
Weston, Lea L. ;
Preteska, Lara G. ;
Snook, Jeremy P. ;
Zhang, Xiaojing ;
Gu, Wei ;
McMurry, Kim ;
Green, Lance D. ;
Chain, Patrick S. ;
Detter, J. Chris ;
Han, Cliff S. .
PLOS ONE, 2012, 7 (05)
[10]   ISOLATION AND DIRECT COMPLETE NUCLEOTIDE DETERMINATION OF ENTIRE GENES - CHARACTERIZATION OF A GENE CODING FOR 16S-RIBOSOMAL RNA [J].
EDWARDS, U ;
ROGALL, T ;
BLOCKER, H ;
EMDE, M ;
BOTTGER, EC .
NUCLEIC ACIDS RESEARCH, 1989, 17 (19) :7843-7853