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Nat Biotechnol ; 37(8): 937-944, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31359005

RESUMEN

Characterization of microbiomes has been enabled by high-throughput metagenomic sequencing. However, existing methods are not designed to combine reads from short- and long-read technologies. We present a hybrid metagenomic assembler named OPERA-MS that integrates assembly-based metagenome clustering with repeat-aware, exact scaffolding to accurately assemble complex communities. Evaluation using defined in vitro and virtual gut microbiomes revealed that OPERA-MS assembles metagenomes with greater base pair accuracy than long-read (>5×; Canu), higher contiguity than short-read (~10× NGA50; MEGAHIT, IDBA-UD, metaSPAdes) and fewer assembly errors than non-metagenomic hybrid assemblers (2×; hybridSPAdes). OPERA-MS provides strain-resolved assembly in the presence of multiple genomes of the same species, high-quality reference genomes for rare species (<1%) with ~9× long-read coverage and near-complete genomes with higher coverage. We used OPERA-MS to assemble 28 gut metagenomes of antibiotic-treated patients, and showed that the inclusion of long nanopore reads produces more contiguous assemblies (200× improvement over short-read assemblies), including more than 80 closed plasmid or phage sequences and a new 263 kbp jumbo phage. High-quality hybrid assemblies enable an exquisitely detailed view of the gut resistome in human patients.


Asunto(s)
Bacterias/efectos de los fármacos , Bacterias/genética , Metagenómica/métodos , Microbiota/efectos de los fármacos , Análisis de Secuencia de ADN/métodos , Antibacterianos/farmacología , Farmacorresistencia Bacteriana , Heces/microbiología , Secuenciación de Nucleótidos de Alto Rendimiento/métodos , Humanos , Metagenoma , Nanoporos , Programas Informáticos
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