The ability to deliver safe medications and vaccines, free of microbial contamination, is dependent on modern methods to identify bacteria that range from biochemical to genotypic in nature. Conventional genotypic methods for bacterial identification generally rely on small parts of the genome, but advancements in DNA sequencing technologies have reduced the time and cost needed to sequence whole genomes. In order to increase resolution in microbial identification and reduce time-to-result compared to conventional methods, we have developed a workflow for rapid identification of bacteria using Oxford Nanopore DNA sequencing that can reconstruct whole genome sequences with >99.8% accuracy to reference sequences. The reconstruction of an entire genome sequence enables high-resolution identification of bacteria. For example, the platform can rapidly differentiate closely related strains of Shigella and E. coli through taxonomic assignment using average nucleotide identity (ANI) and multi-locus sequence typing, and investigations into sub-strain-level differentiation using ANI are ongoing. The analysis of genome data normally requires a highly trained analyst, but work is underway to automate these computational processes as part of Merck's patent-pending ViruScreen platform which enables multi-omic analytical research through an easy-to-use web portal.
Watson et al. (Thu,) studied this question.