SARS-CoV-2 transmission among health care workers, an outbreak investigation using whole-genome sequencing
PLOS ONE
RESEARCH ARTICLE
SARS-CoV-2 transmission among health care
workers, an outbreak investigation using
whole-genome sequencing
K. S. te Paske ID1☯*, C. van Tienen2‡, D Dunk2,3‡, D. van Pelt4‡, P. W. Smit2,3☯
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1 Department of Infectious Disease Control, Municipal Health Service Haaglanden, The Hague, the
Netherlands, 2 Department of Medical Microbiology, Maasstad Hospital, Rotterdam, the Netherlands,
3 Molecular Diagnostic Unit, Maasstad Hospital, Rotterdam, the Netherlands, 4 Department of Occupational
Health, Maasstad Hospital, Rotterdam, the Netherlands
☯ These authors contributed equally to this work.
‡ These authors also contributed equally to this work
*
Abstract
OPEN ACCESS
Citation: te Paske KS, Tienen Cv, Dunk D, Pelt Dv,
Smit PW (2023) SARS-CoV-2 transmission among
health care workers, an outbreak investigation
using whole-genome sequencing. PLoS ONE
18(3): e0283292. https://doi.org/10.1371/journal.
pone.0283292
Editor: Kelli L. Barr, University of South Florida,
UNITED STATES
Received: December 2, 2022
Accepted: February 27, 2023
Background
We report an outbreak investigation to map intra-hospital transmission among health care
workers (HCW) using epidemiological and whole-genome sequencing data.
Methods
Fourteen clinical wards (COVID-19 and non-COVID-19) with high infection rates of SARSCoV-2 among HCW were selected and demographical, epidemiological and sequencing
data were collected of all HCW testing positive by RT-PCR. Clustered cases were identified
based on first disease onsets and differences in single nucleotide polymorphisms (SNP’s)
and were analysed for additional characteristics.
Published: March 31, 2023
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https://doi.org/10.1371/journal.pone.0283292
Copyright: © 2023 te Paske et al. This is an open
access article distributed under the terms of the
Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.
Data Availability Statement: On https://gisaid.org
researchers can download all of the sequencing
data that is used in this article. However one has to
register (free). Our data is named as follows:
Results
Data was collected for 123 HCW. Out of 123 HCW, 65 (53%) worked at eight non-COVID19 wards, 56 (46%) at four COVID-19 wards, one (<1%) worked on several wards and for
one (<1%) it was unknown. One major cluster (n = 34) and three minor clusters (n = 2,3,4;
total n = 9) comprising of 43 HCW (35%) were found after comparing our study population (n
= 123) with the circulating regional sequences (n = 819). In clustered cases work was most
often the suspected source of infection and continuing work while having symptoms
occurred in all clusters, ranging from 1–6 days.
Conclusion
Our findings strongly indicate transmission of SARS-CoV-2 among HCW. Whole-genome
sequencing is useful for identification of clusters and can give direction to targeted infection
prevention measures.
PLOS ONE | https://doi.org/10.1371/journal.pone.0283292 March 31, 2023
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Funding: The author(s) received no specific
funding for this work.
Competing interests: The authors have declared
that no competing interests exist.
SARS-CoV-2 transmission among health care workers
Background
Ever since the first reported case of COVID-19 in February 2020, the Netherlands is dealing
with SARS-CoV-2 and its consequences. The second wave started in July followed by a steep
rise in new daily cases up to 11.000 in December 2020 [1]. National public health measures
were repeatedly intensified and the national testing capacity was constrained due to high
demands [2]. Large numbers of COVID-19 infections among patients and health care workers
(HCW) have posed pressure on all hospitals. Several studies indicate intra-hospital transmission between HCW [3,4]. In response to high infection rates in various clinical wards in one
hospital in the Netherlands, we conducted an epidemiological and genomic outbreak investigation of hospital personnel with COVID-19 to gain insight in intra-hospital transmission.
Methods
Hospital context
This study was performed at one hospital in the Netherlands, during 4 September—31 December 2020. At the time, 6468 hospital employees were employed and 3724 RT-PCR tests were
performed (personnel only) of which 2324 unique employees (S1 Table).
According to hospital policy, all HCW experiencing symptoms consistent with COVID-19
underwent oro-nasopharyngeal swab RT-PCR testing and were instructed to self-isolate.
Awaiting test results, HCW were allowed to work with a surgical mask (type 2R) provided that
symptoms were mild and their work was considered crucial (irreplaceable, indispensable and
working remotely impossible) for continuity of patient care. In case HCW tested positive, they
remained on sick leave until seven or fourteen days (depending on severity of clinical course)
after disease onset and >24 hours free of symptoms. In case mild symptoms remained present,
HCW resumed work after a positive SARS-CoV-2 antibodies test (Wantai, Beijing, China) at
day 10. Personal protective equipment supplies and laboratory testing capacity for personnel
were sufficient.
Study design
Fourteen clinical wards (COVID-19 and non-COVID-19) with positive HCW were selected
and all HCW working in these wards who tested positive for SARS-CoV-2 were enrolled.
Departments with a high likeliness of receiving COVID-19 patients were registered as
COVID-19 wards and the remaining departments as non-COVID-19 wards. The molecular
diagnostic unit performed RT-PCR testing for SARS-CoV-2 and whole genome sequencing.
The occupational health department inventoried demographical and epidemiological data of
positive HCW. The Medical Research Ethics Committees United (MEC-U) waived the need
for ethical approval as samples were collected for routine diagnostic care. Samples and data
were processed anonymously to ensure privacy of our co-workers.
Whole genome sequencing and phylogenetic analysis
RT-PCR was performed on a fast RT-PCR platform (NeumoDx, Qiagen, Germany). Samples with a cycle threshold below 30 were considered for sequencing. Oxford Nanopore
MinION sequencing was performed following ARTICv3 (LoCost) protocol [5], using
R9.04.01 flow cells on a MinIon Mk1b or Mk1C device. Basecalling and demultiplexing was
performed using Guppy and further analysed using medaka for consensus and variant calling according to the ARTIC pipeline [6]. Phylogenetic analysis and data visualization was
done in Pathogen.watch [7].
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