Comparison of long-read sequencing technologies in the hybrid assembly of complex bacterial genomes

长时间测序技术在复杂细菌基因组杂交组装中的比较

作者:

Nicola De Maio,Liam P. Shaw,Alasdair Hubbard,Sophie George,Nicholas D. Sanderson,Jeremy Swann,Ryan Wick,Manal AbuOun,Emma Stubberfield,Sarah J. Hoosdally,Derrick W. Crook,Timothy E. A. Peto,Anna E. Sheppard,Mark J. Bailey,Daniel S. Read,Muna F. Anjum,A. Sarah Walker,Nicole Stoesser,M Abuoun,M Anjum,M Bailey,H Brett,M Bowes,K Chau,DW Crook,N de Maio,N Duggett,D Gilson,HS Gweon,A Hubbard,S Hoosdally,J Kavanaugh,H Jones,TEA Peto,DS Read,R Sebra,LP Shaw,AE Sheppard,R Smith

作者背景:N/A

DOI:10.1099/mgen.0.000294

文章关键词:Hybrid assembly,Bacterial genomics,Long-read sequencing,Enterobacteriaceae,Plasmid assembly

原文摘要:Illumina sequencing allows rapid, cheap and accurate whole genome bacterial analyses, but short reads (<300 bp) do not usually enable complete genome assembly. Long-read sequencing greatly assists with resolving complex bacterial genomes, particularly when combined with short-read Illumina data (hybrid assembly). However, it is not clear how different long-read sequencing methods affect hybrid assembly accuracy. Relative automation of the assembly process is also crucial to facilitating high-throughput complete bacterial genome reconstruction, avoiding multiple bespoke filtering and data manipulation steps. In this study, we compared hybrid assemblies for 20 bacterial isolates, including two reference strains, using Illumina sequencing and long reads from either Oxford Nanopore Technologies (ONT) or SMRT Pacific Biosciences (PacBio) sequencing platforms. We chose isolates from the family Enterobacteriaceae , as these frequently have highly plastic, repetitive genetic structures, and complete genome reconstruction for these species is relevant for a precise understanding of the epidemiology of antimicrobial resistance. We de novo assembled genomes using the hybrid assembler Unicycler and compared different read processing strategies, as well as comparing to long-read-only assembly with Flye followed by short-read polishing with Pilon. Hybrid assembly with either PacBio or ONT reads facilitated high-quality genome reconstruction, and was superior to the long-read assembly and polishing approach evaluated with respect to accuracy and completeness. Combining ONT and Illumina reads fully resolved most genomes without additional manual steps, and at a lower consumables cost per isolate in our setting. Automated hybrid assembly is a powerful tool for complete and accurate bacterial genome assembly.

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