Evidence map›Paper›PMID 34835057›Full record

ArticleViruses2021

Development of a Hamster Natural Transmission Model of SARS-CoV-2 Infection.

Stuart Dowall, Francisco J Salguero, Nathan Wiblin, Susan Fotheringham, Graham Hatch, Simon Parks, Kathryn Gowan, Debbie Harris, Oliver Carnell, Rachel Fell and 6 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 14% of its field
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

19 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Stuart DowallUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Francisco J SalgueroUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.ORCID 0000-0002-5315-3882
Nathan WiblinUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Susan FotheringhamUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Graham HatchUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Simon ParksUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Kathryn GowanUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Debbie HarrisUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Oliver CarnellUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Rachel FellUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Robert WatsonUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Victoria GrahamUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Karen GoochUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Yper HallUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.
Simon MizenTecniplast UK Ltd., BCM Box 3058, London WC1N 3XX, UK.
Roger HewsonUnited Kingdom Health Security Agency (UKHSA), Porton Down, Salisbury SP4 0JG, UK.

Funding

Medical Research Council MR/V036963/1National Institute for Health Research MR/V036963/1UK Research and Innovation MR/V036963/1
6 · The paper itself

Abstract

The global pandemic of coronavirus disease (COVID-19) caused by infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has led to an international thrust to study pathogenesis and evaluate interventions. Experimental infection of hamsters and the resulting respiratory disease is one of the preferred animal models since clinical signs of disease and virus shedding are similar to more severe cases of human COVID-19. The main route of challenge has been direct inoculation of the virus via the intranasal route. To resemble the natural infection, we designed a bespoke natural transmission cage system to assess whether recipient animals housed in physically separate adjacent cages could become infected from a challenged donor animal in a central cage, with equal airflow across the two side cages. To optimise viral shedding in the donor animals, a low and moderate challenge dose were compared after direct intranasal challenge, but similar viral shedding responses were observed and no discernible difference in kinetics. The results from our natural transmission set-up demonstrate that most recipient hamsters are infected within the system developed, with variation in the kinetics and levels of disease between individual animals. Common clinical outputs used for the assessment in directly-challenged hamsters, such as weight loss, are less obvious in hamsters who become infected from naturally acquiring the infection. The results demonstrate the utility of a natural transmission model for further work on assessing the differences between virus strains and evaluating interventions using a challenge system which more closely resembles human infection.

Indexed as

Disease Models, AnimalMesocricetusAnimalsCOVID-19CricetinaeFemaleLungMaleNasal CavitySARS-CoV-2Viral LoadVirus SheddinganimalsCOVID-19transmission

Identifiers

PMID34835057
PMCPMC8625437
OpenAlexW3213721870

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.