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Updated: Nov 20, 2025

Isolation and Genome Analysis of Single Virions using 'Single Virus Genomics'
Published on: May 26, 2013
Isolating SARS-CoV-2 Strains From Countries in the Same Meridian: Genome Evolutionary Analysis
Emilio Mastriani1,2, Alexey V Rakov3, Shu-Lin Liu1,2,4
1Systemomics Center, College of Pharmacy, Genomics Research Center, State-Province Key Laboratories of Biomedicine-Pharmaceutics of China, Harbin Medical University, Harbin, China.
Genomic analysis of SARS-CoV-2 strains revealed a key mutation (codon 9628) influencing viral attachment. This finding aids in developing effective vaccines and antiviral strategies against COVID-19.
Area of Science:
- Virology
- Genomics
- Molecular Biology
Background:
- COVID-19, caused by SARS-CoV-2, is a global health threat with significant mortality.
- SARS-CoV-2 strains exhibit geographic and genomic specificity, with potential variations in clinical features.
- Previous genomic comparisons identified distinct clades in Europe, Asia, and North America.
Purpose of the Study:
- To compare SARS-CoV-2 genomes from Italy, Sweden, Congo, and Brazil.
- To analyze evolutionary pressure signatures in viral genomes across different geographical and climatic conditions.
- To investigate potential differences in SARS-CoV-2 evolution.
Main Methods:
- Genome data acquisition from GISAID.
- Phylogenetic and evolutionary analyses using HyPhy (genetic algorithm recombination detection, mixed effects model of evolution).
- Secondary structure prediction, disorder, transmembrane analyses, and ab initio protein structure prediction.
Main Results:
- Codon 9628 identified as under episodic selective pressure across all analyzed SARS-CoV-2 strains.
- Mutation at codon 9628 affects the secondary structure of the P0DTD3 protein, influencing helical modification.
- The mutation enhances protein binding probability and may be involved in viral attachment.
Conclusions:
- A specific mutation (codon 9628) impacts SARS-CoV-2 RNA secondary structure and protein function.
- Amino acid changes (T to G, G to D) may enhance viral binding to human cells.
- Findings support the development of targeted in vitro experiments, vaccines, and antiviral therapies.
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