Phylo-Plex: A phylogenetically informed, low-cost amplicon sequencing platform for deployable high-resolution genomic epidemiology
Beale, M. A.; Shetty, V.; Ambridge, K. E.; Lacey, G.; Dougan, S.; Roberts-Sengier, W.; Sampher, B.; Lassalle, F.; Dorman, M. J.; Mahlangu, M. P.; Venter, J. M.; Da Costa Dias, B.; Chipinduro, M.; Washaya, T. M.; Rodgers, L.; Makamure, B.; Dauya, E.; Marks, M.; Muller, E.; Ferrand, R. A.; Thomson, N. R.
Show abstract
Genomic pathogen surveillance is a powerful tool for public health and research, but is costly and unachievable in low-resource settings. Most sub-genomic typing methods sacrifice resolution whilst remaining costly. We developed "Phylo-Plex", a novel approach that identifies information-rich genomic regions to maximise phylogenetic information whilst minimising the number of regions. Applied to Treponema pallidum and Neisseria gonorrhoeae, we designed a high-resolution multiplex PCR sequencing scheme for lineage tracking pathogens with different extremes of genome variation. For Treponema pallidum, we also designed and evaluated the Phylo-Plex scheme in the laboratory and field settings by sequencing 72 clinical samples using MinION Flongle cells. Our T. pallidum scheme comprising 59 multiplex amplicons achieved high discrimination of fine-scale sublineages comparable to those defined using whole genomes, and demonstrating a qPCR detection limit [≤]Ct 32. Variant calls from MinION amplicon sequencing were highly correlated with Illumina whole genome sequencing. We successfully deployed the method in a low-resource laboratory in Zimbabwe, costed at <{pound}300/24 samples ({pound}12.47/sample). Phylo-Plex enables low-cost tracking of priority pathogenic lineages in low resource settings and at scale.
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