Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State

Abstract Background Long-term care facilities (LTCFs) are vulnerable to disease outbreaks. Here, we jointly analyze SARS-CoV-2 genomic and paired epidemiologic data from LTCFs and surrounding communities in Washington state (WA) to assess transmission patterns during 2020–2022, in a setting of chang...

Full description

Bibliographic Details
Main Authors: Hanna N. Oltean, Allison Black, Stephanie M. Lunn, Nailah Smith, Allison Templeton, Elyse Bevers, Lynae Kibiger, Melissa Sixberry, Josina B. Bickel, James P. Hughes, Scott Lindquist, Janet G. Baseman, Trevor Bedford
Format: Article
Language:English
Published: BMC 2024-01-01
Series:BMC Public Health
Subjects:
Online Access:https://doi.org/10.1186/s12889-023-17461-2
_version_ 1797349666657927168
author Hanna N. Oltean
Allison Black
Stephanie M. Lunn
Nailah Smith
Allison Templeton
Elyse Bevers
Lynae Kibiger
Melissa Sixberry
Josina B. Bickel
James P. Hughes
Scott Lindquist
Janet G. Baseman
Trevor Bedford
author_facet Hanna N. Oltean
Allison Black
Stephanie M. Lunn
Nailah Smith
Allison Templeton
Elyse Bevers
Lynae Kibiger
Melissa Sixberry
Josina B. Bickel
James P. Hughes
Scott Lindquist
Janet G. Baseman
Trevor Bedford
author_sort Hanna N. Oltean
collection DOAJ
description Abstract Background Long-term care facilities (LTCFs) are vulnerable to disease outbreaks. Here, we jointly analyze SARS-CoV-2 genomic and paired epidemiologic data from LTCFs and surrounding communities in Washington state (WA) to assess transmission patterns during 2020–2022, in a setting of changing policy. We describe sequencing efforts and genomic epidemiologic findings across LTCFs and perform in-depth analysis in a single county. Methods We assessed genomic data representativeness, built phylogenetic trees, and conducted discrete trait analysis to estimate introduction sizes over time, and explored selected outbreaks to further characterize transmission events. Results We found that transmission dynamics among cases associated with LTCFs in WA changed over the course of the COVID-19 pandemic, with variable introduction rates into LTCFs, but decreasing amplification within LTCFs. SARS-CoV-2 lineages circulating in LTCFs were similar to those circulating in communities at the same time. Transmission between staff and residents was bi-directional. Conclusions Understanding transmission dynamics within and between LTCFs using genomic epidemiology on a broad scale can assist in targeting policies and prevention efforts. Tracking facility-level outbreaks can help differentiate intra-facility outbreaks from high community transmission with repeated introduction events. Based on our study findings, methods for routine tree building and overlay of epidemiologic data for hypothesis generation by public health practitioners are recommended. Discrete trait analysis added valuable insight and can be considered when representative sequencing is performed. Cluster detection tools, especially those that rely on distance thresholds, may be of more limited use given current data capture and timeliness. Importantly, we noted a decrease in data capture from LTCFs over time. Depending on goals for use of genomic data, sentinel surveillance should be increased or targeted surveillance implemented to ensure available data for analysis.
first_indexed 2024-03-08T12:33:42Z
format Article
id doaj.art-ab8ecfbcc2504dbfa6dac0d4ec7acfa6
institution Directory Open Access Journal
issn 1471-2458
language English
last_indexed 2024-03-08T12:33:42Z
publishDate 2024-01-01
publisher BMC
record_format Article
series BMC Public Health
spelling doaj.art-ab8ecfbcc2504dbfa6dac0d4ec7acfa62024-01-21T12:38:25ZengBMCBMC Public Health1471-24582024-01-0124111210.1186/s12889-023-17461-2Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington StateHanna N. Oltean0Allison Black1Stephanie M. Lunn2Nailah Smith3Allison Templeton4Elyse Bevers5Lynae Kibiger6Melissa Sixberry7Josina B. Bickel8James P. Hughes9Scott Lindquist10Janet G. Baseman11Trevor Bedford12Department of Health, Washington StateDepartment of Health, Washington StateDepartment of Health, Washington StateDepartment of Health, Washington StateDepartment of Health, Washington StateDepartment of Health, Washington StateDepartment of Health, Washington StateYakima Health DistrictYakima Health DistrictUniversity of WashingtonDepartment of Health, Washington StateUniversity of WashingtonFred Hutchinson Cancer Research CenterAbstract Background Long-term care facilities (LTCFs) are vulnerable to disease outbreaks. Here, we jointly analyze SARS-CoV-2 genomic and paired epidemiologic data from LTCFs and surrounding communities in Washington state (WA) to assess transmission patterns during 2020–2022, in a setting of changing policy. We describe sequencing efforts and genomic epidemiologic findings across LTCFs and perform in-depth analysis in a single county. Methods We assessed genomic data representativeness, built phylogenetic trees, and conducted discrete trait analysis to estimate introduction sizes over time, and explored selected outbreaks to further characterize transmission events. Results We found that transmission dynamics among cases associated with LTCFs in WA changed over the course of the COVID-19 pandemic, with variable introduction rates into LTCFs, but decreasing amplification within LTCFs. SARS-CoV-2 lineages circulating in LTCFs were similar to those circulating in communities at the same time. Transmission between staff and residents was bi-directional. Conclusions Understanding transmission dynamics within and between LTCFs using genomic epidemiology on a broad scale can assist in targeting policies and prevention efforts. Tracking facility-level outbreaks can help differentiate intra-facility outbreaks from high community transmission with repeated introduction events. Based on our study findings, methods for routine tree building and overlay of epidemiologic data for hypothesis generation by public health practitioners are recommended. Discrete trait analysis added valuable insight and can be considered when representative sequencing is performed. Cluster detection tools, especially those that rely on distance thresholds, may be of more limited use given current data capture and timeliness. Importantly, we noted a decrease in data capture from LTCFs over time. Depending on goals for use of genomic data, sentinel surveillance should be increased or targeted surveillance implemented to ensure available data for analysis.https://doi.org/10.1186/s12889-023-17461-2EpidemiologySurveillanceSARS-CoV-2GenomicsHealthcare-associated InfectionsPublic health
spellingShingle Hanna N. Oltean
Allison Black
Stephanie M. Lunn
Nailah Smith
Allison Templeton
Elyse Bevers
Lynae Kibiger
Melissa Sixberry
Josina B. Bickel
James P. Hughes
Scott Lindquist
Janet G. Baseman
Trevor Bedford
Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
BMC Public Health
Epidemiology
Surveillance
SARS-CoV-2
Genomics
Healthcare-associated Infections
Public health
title Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
title_full Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
title_fullStr Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
title_full_unstemmed Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
title_short Changing genomic epidemiology of COVID-19 in long-term care facilities during the 2020–2022 pandemic, Washington State
title_sort changing genomic epidemiology of covid 19 in long term care facilities during the 2020 2022 pandemic washington state
topic Epidemiology
Surveillance
SARS-CoV-2
Genomics
Healthcare-associated Infections
Public health
url https://doi.org/10.1186/s12889-023-17461-2
work_keys_str_mv AT hannanoltean changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT allisonblack changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT stephaniemlunn changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT nailahsmith changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT allisontempleton changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT elysebevers changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT lynaekibiger changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT melissasixberry changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT josinabbickel changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT jamesphughes changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT scottlindquist changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT janetgbaseman changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate
AT trevorbedford changinggenomicepidemiologyofcovid19inlongtermcarefacilitiesduringthe20202022pandemicwashingtonstate