4.7 Article

Epidemiological data and genome sequencing reveals that nosocomial transmission of SARS-CoV-2 is underestimated and mostly mediated by a small number of highly infectious individuals

期刊

JOURNAL OF INFECTION
卷 83, 期 4, 页码 473-482

出版社

W B SAUNDERS CO LTD
DOI: 10.1016/j.jinf.2021.07.034

关键词

Whole genome sequencing; Epidemiology; SARS-CoV-2; Nosocomial infection

资金

  1. National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Healthcare Associated Infections and Antimicrobial Resistance at Oxford University
  2. Public Health England (PHE), the NIHR Biomedical Research Centre, Oxford [NIHR200915]
  3. Wellcome Intermediate Fellowship [110,110/Z/15/Z, 214,560/Z/18/Z]
  4. [MRF-145-00 04-TPG-AVISO]

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This study investigated the epidemiological characteristics of healthcare-associated SARS-CoV-2 acquisition. The findings suggest that current surveillance definitions underestimate nosocomial acquisition, with most nosocomial transmission occurring from a relatively limited number of highly infectious individuals.
Objectives: Despite robust efforts, patients and staffacquire SARS-CoV-2 infection in hospitals. We investigated whether whole-genome sequencing enhanced the epidemiological investigation of healthcare-associated SARS-CoV-2 acquisition. Methods: From 17-November-2020 to 5-January-2021, 803 inpatients and 329 staff were diagnosed with SARS-CoV-2 infection at four Oxfordshire hospitals. We classified cases using epidemiological definitions, looked for a potential source for each nosocomial infection, and evaluated genomic evidence supporting transmission. Results: Using national epidemiological definitions, 109/803(14%) inpatient infections were classified as definite/probable nosocomial, 615(77%) as community-acquired and 79(10%) as indeterminate. There was strong epidemiological evidence to support definite/probable cases as nosocomial. Many indeterminate cases were likely infected in hospital: 53/79(67%) had a prior-negative PCR and 75(95%) contact with a potential source. 89/615(11% of all 803 patients) with apparent community-onset had a recent hospital exposure. Within 764 samples sequenced 607 genomic clusters were identified (>1 SNP distinct). Only 43/607(7%) clusters contained evidence of onward transmission (subsequent cases within <= 1 SNP). 20/21 epidemiologically-identified outbreaks contained multiple genomic introductions. Most (80%) nosocomial acquisition occurred in rapid super-spreading events in settings with a mix of COVID-19 and non-COVID-19 patients. Conclusions: Current surveillance definitions underestimate nosocomial acquisition. Most nosocomial transmission occurs from a relatively limited number of highly infectious individuals. (C) 2021 The Authors. Published by Elsevier Ltd on behalf of The British Infection Association.

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