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Co-infection with SARS-CoV-2 Omicron and Delta variants revealed by genomic surveillance.
Rockett, Rebecca J; Draper, Jenny; Gall, Mailie; Sim, Eby M; Arnott, Alicia; Agius, Jessica E; Johnson-Mackinnon, Jessica; Fong, Winkie; Martinez, Elena; Drew, Alexander P; Lee, Clement; Ngo, Christine; Ramsperger, Marc; Ginn, Andrew N; Wang, Qinning; Fennell, Michael; Ko, Danny; Hueston, Linda; Kairaitis, Lukas; Holmes, Edward C; O'Sullivan, Matthew N; Chen, Sharon C-A; Kok, Jen; Dwyer, Dominic E; Sintchenko, Vitali.
  • Rockett RJ; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Draper J; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Gall M; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Sim EM; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Arnott A; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Agius JE; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Johnson-Mackinnon J; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Fong W; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Martinez E; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Drew AP; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Lee C; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Ngo C; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Ramsperger M; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Ginn AN; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Wang Q; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Fennell M; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Ko D; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Hueston L; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
  • Kairaitis L; Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
  • Holmes EC; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • O'Sullivan MN; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Chen SC; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Kok J; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Dwyer DE; Institute for Clinical Pathology and Medical Research, New South Wales Health Pathology, Westmead, NSW, Australia.
  • Sintchenko V; Sydney Institute for Infectious Diseases, University of Sydney, Sydney, NSW, Australia.
Nat Commun ; 13(1): 2745, 2022 05 18.
Article in English | MEDLINE | ID: covidwho-1931393
ABSTRACT
Co-infections with different variants of SARS-CoV-2 are a key precursor to recombination events that are likely to drive SARS-CoV-2 evolution. Rapid identification of such co-infections is required to determine their frequency in the community, particularly in populations at-risk of severe COVID-19, which have already been identified as incubators for punctuated evolutionary events. However, limited data and tools are currently available to detect and characterise the SARS-CoV-2 co-infections associated with recognised variants of concern. Here we describe co-infection with the SARS-CoV-2 variants of concern Omicron and Delta in two epidemiologically unrelated adult patients with chronic kidney disease requiring maintenance haemodialysis. Both variants were co-circulating in the community at the time of detection. Genomic surveillance based on amplicon- and probe-based sequencing using short- and long-read technologies identified and quantified subpopulations of Delta and Omicron viruses in respiratory samples. These findings highlight the importance of integrated genomic surveillance in vulnerable populations and provide diagnostic pathways to recognise SARS-CoV-2 co-infection using genomic data.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coinfection / COVID-19 Type of study: Prognostic study Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-30518-x

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coinfection / COVID-19 Type of study: Prognostic study Topics: Variants Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2022 Document Type: Article Affiliation country: S41467-022-30518-x