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Evidence of recurrent selection of mutations commonly found in SARS-CoV-2 variants of concern in viruses infecting immunocompromised patients.
Goes, Livia R; Siqueira, Juliana D; Garrido, Marianne M; Alves, Brunna M; Cicala, Claudia; Arthos, James; Viola, João P B; Soares, Marcelo A.
  • Goes LR; Oncovirology Program, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
  • Siqueira JD; Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States.
  • Garrido MM; Oncovirology Program, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
  • Alves BM; Hospital Infection Control Committee, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
  • Cicala C; Oncovirology Program, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
  • Arthos J; Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States.
  • Viola JPB; Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, Bethesda, MD, United States.
  • Soares MA; Immunology and Tumor Biology Program, Brazilian National Cancer Institute, Rio de Janeiro, Brazil.
Front Microbiol ; 13: 946549, 2022.
Article in English | MEDLINE | ID: covidwho-1993801
ABSTRACT
Chronically immunosuppressed patients infected with SARS-CoV-2 often experience prolonged virus shedding, and may pave the way to the emergence of mutations that render viral variants of concern (VOC) able to escape immune responses induced by natural infection or by vaccination. We report herein a SARS-CoV-2+ cancer patient from the beginning of the COVID-19 pandemic whose virus quasispecies across multiple timepoints carried several immune escape mutations found in more contemporary VOC, such as alpha, delta and omicron, that appeared to be selected for during infection. We hypothesize that immunosuppressed patients may represent the source of VOC seen throughout the COVID-19 pandemics.
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Full text: Available Collection: International databases Database: MEDLINE Topics: Vaccines / Variants Language: English Journal: Front Microbiol Year: 2022 Document Type: Article Affiliation country: Fmicb.2022.946549

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Full text: Available Collection: International databases Database: MEDLINE Topics: Vaccines / Variants Language: English Journal: Front Microbiol Year: 2022 Document Type: Article Affiliation country: Fmicb.2022.946549