<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Zhang C</submitter><funding>National Natural Science Foundation of China</funding><pubmed_abstract>The mutation pattern of severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has changed constantly during worldwide community transmission of this virus. However, the reasons for the changes in mutation patterns are still unclear. Accordingly, in this study, we present a comprehensive analysis of over 300 million peptides derived from 13,432 SARS-CoV-2 strains harboring 4,420 amino acid mutations to analyze the potential selective pressure of the host immune system and reveal the driver of mutations in circulating SARS-CoV-2 isolates. The results showed that the nonstructural protein ORF1ab and the structural protein Spike were most susceptible to mutations. Furthermore, mutations in cross-reactive T-cell epitopes between SARS-CoV-2 and seasonal human coronavirus may help SARS-CoV</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>599562</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8169977</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Antigenic Evolution on a Global Scale Reveals the Potential Natural Selection of Severe Acute Respiratory Syndrome-Coronavirus 2 by Pre-existing Cross-Reactive T-Cell Immunity.</pubmed_title><pmcid>PMC8169977</pmcid><pubmed_authors>Leng Q</pubmed_authors><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Qiu T</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Qiu L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antigenic Evolution on a Global Scale Reveals the Potential Natural Selection of Severe Acute Respiratory Syndrome-Coronavirus 2 by Pre-existing Cross-Reactive T-Cell Immunity.</name><description>The mutation pattern of severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has changed constantly during worldwide community transmission of this virus. However, the reasons for the changes in mutation patterns are still unclear. Accordingly, in this study, we present a comprehensive analysis of over 300 million peptides derived from 13,432 SARS-CoV-2 strains harboring 4,420 amino acid mutations to analyze the potential selective pressure of the host immune system and reveal the driver of mutations in circulating SARS-CoV-2 isolates. The results showed that the nonstructural protein ORF1ab and the structural protein Spike were most susceptible to mutations. Furthermore, mutations in cross-reactive T-cell epitopes between SARS-CoV-2 and seasonal human coronavirus may help SARS-CoV</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T01:22:43.639Z</modification><creation>2022-02-10T14:11:26.569Z</creation></dates><accession>S-EPMC8169977</accession><cross_references><pubmed>34093454</pubmed><doi>10.3389/fmicb.2021.599562</doi></cross_references></HashMap>