Related Experiment Video
Updated: Dec 26, 2025

18:10
Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
Published on: June 16, 2011
30.0K
The establishment of reference sequence for SARS-CoV-2 and variation analysis.
Changtai Wang1,2,3, Zhongping Liu1,2, Zixiang Chen2
1Department of Infectious Diseases, The Second Hospital of Anhui Medical University, Hefei, China.
Journal of Medical Virology
|March 14, 2020
Summary
Genetic analysis of 95 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) strains revealed high genomic homology. Researchers identified key mutation sites, crucial for developing accurate diagnostic tools and interventions for COVID-19.
Area of Science:
- Virology
- Genomics
- Epidemiology
Background:
- The COVID-19 pandemic, caused by SARS-CoV-2, emerged in late 2019.
- Limited sensitivity of current nucleic acid detection methods necessitates further investigation.
- The role of genetic variation in SARS-CoV-2 is not fully understood.
Purpose of the Study:
- To analyze sequence variations in SARS-CoV-2 genomes.
- To establish a reference sequence for SARS-CoV-2.
- To identify potential mutation sites for diagnostic and therapeutic development.
Main Methods:
- Retrieved 95 full-length SARS-CoV-2 genomic sequences from public databases (NCBI and GISAID).
- Performed multiple sequence alignment and phylogenetic analyses to establish a reference sequence.
- Analyzed sequence variations across the viral genome, focusing on open-reading frames (ORFs).
Main Results:
- High genomic homology observed among SARS-CoV-2 strains (nucleotide and amino acid levels).
- Identified 13 variation sites across multiple genomic regions (1a, 1b, S, 3a, M, 8, and N).
- Noted significant mutation rates at nt28144 in ORF 8 (30.53%) and nt8782 in ORF 1a (29.47%).
Conclusions:
- Selective mutations may exist within the SARS-CoV-2 genome.
- Identified mutation sites are critical for primer and probe design in diagnostic assays.
- Establishing a SARS-CoV-2 reference sequence aids biological study, diagnosis, and clinical management.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
17.7K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.7K
Sanger Sequencing
772.2K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
772.2K
Evolutionary Relationships through Genome Comparisons
6.8K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.8K

