Abstract
Bacterial plasmids play a major role in the spread of antibiotic resistance genes. However, their characterization via DNA sequencing suffers from the small proportion of plasmid DNA in those samples. Although sample preparation methods can enrich the proportion of plasmid DNA before sequencing, these methods are expensive and laborious, and they might introduce a bias by enriching only for specific plasmid DNA sequences. Nanopore adaptive sampling could overcome these issues by rejecting uninteresting DNA molecules during the sequencing process. In this study, we assess the application of adaptive sampling for the enrichment of low abundant plasmids in known bacterial isolates using two different adaptive sampling tools. We further inspect potential cost savings for laboratories by utilizing adaptive sampling on reused or expired flow cells. We show that a significant enrichment can be achieved even on reused or expired flow cells. By applying adaptive sampling, we also improve the quality of de novo plasmid assemblies and reduce the sequencing time. Our experiments indicate that the choice of the read classification method and read lengths used for the classification influence the enrichment factor.
Competing Interest Statement
JUU and BYR have filed a patent application on selective nanopore sequencing approaches.
