Evidence map›Paper›PMID 39072023›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Spatial and temporal transmission dynamics of respiratory syncytial virus in New Zealand before and after the COVID-19 pandemic.

Lauren Jelley, Jordan Douglas, Meaghan O'Neill, Klarysse Berquist, Ana Claasen, Jing Wang, Srushti Utekar, Helen Johnston, Judy Bocacao, Margot Allais and 18 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Lauren JelleyInstitute of Environmental Science and Research, Wellington, New Zealand.
Jordan DouglasCentre for Computational Evolution, University of Auckland, Auckland, New Zealand.
Meaghan O'NeillInstitute of Environmental Science and Research, Wellington, New Zealand.
Klarysse BerquistInstitute of Environmental Science and Research, Wellington, New Zealand.
Ana ClaasenInstitute of Environmental Science and Research, Wellington, New Zealand.
Jing WangInstitute of Environmental Science and Research, Wellington, New Zealand.
Srushti UtekarInstitute of Environmental Science and Research, Wellington, New Zealand.
Helen JohnstonInstitute of Environmental Science and Research, Wellington, New Zealand.
Judy BocacaoInstitute of Environmental Science and Research, Wellington, New Zealand.
Margot AllaisInstitute of Environmental Science and Research, Wellington, New Zealand.
Joep de LigtInstitute of Environmental Science and Research, Wellington, New Zealand.
Chor Ee TanInstitute of Environmental Science and Research, Wellington, New Zealand.
Ruth SeedsInstitute of Environmental Science and Research, Wellington, New Zealand.
Tim WoodInstitute of Environmental Science and Research, Wellington, New Zealand.
Nayyereh AminisaniInstitute of Environmental Science and Research, Wellington, New Zealand.
Tineke JenningsRegional Public Health, Te Whatu Ora - Health New Zealand Capital, Coast and Hutt Valley, Wellington, New Zealand.
David WelchCentre for Computational Evolution, University of Auckland, Auckland, New Zealand.
Nikki TurnerDepartment of General Practice and Primary Care, University of Auckland, Auckland, New Zealand.
Peter McIntyreDepartment of Primary Health Care and General Practice, University of Otago, Dunedin, New Zealand.
Tony DowellDepartment of Primary Health Care and General Practice, University of Otago, Dunedin, New Zealand.
Adrian TrenholmeTe Whatu Ora-Health New Zealand Counties Manukau, Auckland, New Zealand.
Cass ByrnesTe Whatu Ora-Health New Zealand Counties Manukau, Auckland, New Zealand.
SHIVERS investigation team
Richard WebbyDepartment of Host-Microbe Interactions, St Jude Children's Research Hospital, Memphis, USA.
Nigel FrenchTāwharau Ora/School of Veterinary Science, Massey University, Palmerston North, New Zealand.
David WinterInstitute of Environmental Science and Research, Wellington, New Zealand.
Q Sue HuangInstitute of Environmental Science and Research, Wellington, New Zealand.ORCID 0000-0002-3923-5195
Jemma L GeogheganInstitute of Environmental Science and Research, Wellington, New Zealand.

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
Household Respiratory Virus SARS-CoV-2 Transmission and Immunity Sub-Study (HRTS)U01AI144616 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GORDON, AUBREE L, THOMAS, PAUL G. · 2019 to 2025
$43.7M
NIAID NIH HHS 75N93021C00016NIAID NIH HHS U01 AI144616
6 · The paper itself

Abstract

Human respiratory syncytial virus (RSV) is a major cause of acute respiratory infection. In 2020, RSV was effectively eliminated from the community in New Zealand due to non-pharmaceutical interventions (NPI) used to control the spread of COVID-19. However, in April 2021, following a brief quarantine-free travel agreement with Australia, there was a large-scale nationwide outbreak of RSV that led to reported cases more than five times higher, and hospitalisations more than three times higher, than the typical seasonal pattern. In this study, we generated 1,471 viral genomes of both RSV-A and RSV-B sampled between 2015 and 2022 from across New Zealand. Using a phylodynamics approach, we used these data to better understand RSV transmission patterns in New Zealand prior to 2020, and how RSV became re-established in the community following the relaxation of COVID-19 restrictions. We found that in 2021, there was a large epidemic of RSV in New Zealand that affected a broader age group range compared to the usual pattern of RSV infections. This epidemic was due to an increase in RSV importations, leading to several large genomic clusters of both RSV-A ON1 and RSV-B BA9 genotypes in New Zealand. However, while a number of importations were detected, there was also a major reduction in RSV genetic diversity compared to pre-pandemic seasonal outbreaks. These genomic clusters were temporally associated with the increase of migration in 2021 due to quarantine-free travel from Australia at the time. The closest genetic relatives to the New Zealand RSV genomes, when sampled, were viral genomes sampled in Australia during a large, off-season summer outbreak several months prior, rather than cryptic lineages that were sustained but not detected in New Zealand. These data reveal the impact of NPI used during the COVID-19 pandemic on other respiratory infections and highlight the important insights that can be gained from viral genomes.

Indexed as

disease outbreakgenomic epidemiologyNew ZealandphylodynamicsRespiratory syncytial virusRSVvirus evolution

Identifiers

PMID39072023
PMCPMC11275701

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.