Episode 55: SARS-CoV-2 And Sequencing Spike With Sanger Sequencing - Welcome To 1995
📅8 April 2021
⏱️00:29:03
🎙️Microbial Bioinformatics
👥Guests
Researcher in Computational Biology, Technical University of Denmark
Tue Sparholt Jørgensen
Researcher in Microbial Genomics, Technical University of Denmark
The microbinfie podcast explores an innovative method for rapid COVID-19 variant identification using Sanger sequencing, developed at the Technical University of Denmark to quickly detect and report variants of concern.
Resources
- Preprint: Link to preprint on medRxiv
- Protocol: Sanger sequencing of a part of the SARS-CoV-2 spike
- Software: GitHub repository for COVID spike classification software
- Web App: SSI BioLib COVID Spike Classification App
Note: The method discussed is specific to the spike protein of SARS-CoV-2, and emphasizes the use of Sanger sequencing for variant identification.
Key Points
1. Rapid Variant Detection Method
- Developed a simplified Sanger sequencing approach for COVID-19 variant screening
- Uses existing RT-PCR infrastructure and ARTIC protocol primers
- Can process up to 200 samples per day with minimal additional resources
2. Detection and Reporting Process
- Targets a 1,001-base region in the spike protein
- Results available within 50-60 hours from sample collection
- Immediate reporting to hospitals and contact tracing authorities
3. Practical Implementation
- Initially focused on detecting B.1.1.7 variant
- Successfully identified first P1 variant in Denmark
- Serves as a preliminary screening before whole genome sequencing
Take-Home Messages
- Rapid, accessible method for COVID-19 variant tracking
- Simplifies variant detection using existing laboratory infrastructure
- Enables quick public health response to emerging variants