RAPID prep : A Simple, Fast Protocol for RNA Metagenomic Sequencing of Clinical Samples.
Rachel L TullochKaran KimChisha T SikazweAlice MichieRebecca BurrellEdward C HolmesDominic E DwyerPhilip N BrittonJen KokJohn-Sebastian EdenPublished in: Viruses (2023)
Emerging infectious disease threats require rapid response tools to inform diagnostics, treatment, and outbreak control. RNA-based metagenomics offers this; however, most approaches are time-consuming and laborious. Here, we present a simple and fast protocol, the RAPID prep assay, with the aim of providing a cause-agnostic laboratory diagnosis of infection within 24 h of sample collection by sequencing ribosomal RNA-depleted total RNA. The method is based on the synthesis and amplification of double-stranded cDNA followed by short-read sequencing, with minimal handling and clean-up steps to improve processing time. The approach was optimized and applied to a range of clinical respiratory samples to demonstrate diagnostic and quantitative performance. Our results showed robust depletion of both human and microbial rRNA, and library amplification across different sample types, qualities, and extraction kits using a single workflow without input nucleic-acid quantification or quality assessment. Furthermore, we demonstrated the genomic yield of both known and undiagnosed pathogens with complete genomes recovered in most cases to inform molecular epidemiological investigations and vaccine design. The RAPID prep assay is a simple and effective tool, and representative of an important shift toward the integration of modern genomic techniques with infectious disease investigations.
Keyphrases
- nucleic acid
- infectious diseases
- men who have sex with men
- single cell
- loop mediated isothermal amplification
- high throughput
- randomized controlled trial
- endothelial cells
- copy number
- microbial community
- electronic health record
- cross sectional
- wastewater treatment
- single molecule
- gram negative
- multidrug resistant
- pluripotent stem cells