Evidence map›Paper›PMID 16605302›Full record

ArticlePLoS medicine2006

Cynomolgus macaque as an animal model for severe acute respiratory syndrome.

James V Lawler, Timothy P Endy, Lisa E Hensley, Aura Garrison, Elizabeth A Fritz, May Lesar, Ralph S Baric, David A Kulesh, David A Norwood, Leonard P Wasieloski and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS medicine, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. A Meta-Analysis of Rhesus Macaques (Comparative medicine · 2021
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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 1 country.

James V LawlerInfectious Diseases Department, National Naval Medical Center, Bethesda, Maryland, United States of America.
Timothy P Endy
Lisa E Hensley
Aura Garrison
Elizabeth A Fritz
May Lesar
Ralph S Baric
David A Kulesh
David A Norwood
Leonard P Wasieloski
Melanie P Ulrich
Tom R Slezak
Elizabeth Vitalis
John W Huggins
Peter B Jahrling
Jason Paragas
United States Army Medical Research Institute of Infectious Diseases · USLawrence Livermore National Laboratory · USNaval Medical Research Command · USUniversity of North Carolina at Chapel Hill · USWalter Reed National Military Medical Center · US

Funding

SARS Reverse GeneticsR01AI059136 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BARIC, RALPH S · 2004 to 2008
$1.4M
NIAID NIH HHS AI059136NIAID NIH HHS R01 AI059136
6 · The paper itself

Abstract

backgroundThe emergence of severe acute respiratory syndrome (SARS) in 2002 and 2003 affected global health and caused major economic disruption. Adequate animal models are required to study the underlying pathogenesis of SARS-associated coronavirus (SARS-CoV) infection and to develop effective vaccines and therapeutics. We report the first findings of measurable clinical disease in nonhuman primates (NHPs) infected with SARS-CoV. METHODS AND

findingsIn order to characterize clinically relevant parameters of SARS-CoV infection in NHPs, we infected cynomolgus macaques with SARS-CoV in three groups: Group I was infected in the nares and bronchus, group II in the nares and conjunctiva, and group III intravenously. Nonhuman primates in groups I and II developed mild to moderate symptomatic illness. All NHPs demonstrated evidence of viral replication and developed neutralizing antibodies. Chest radiographs from several animals in groups I and II revealed unifocal or multifocal pneumonia that peaked between days 8 and 10 postinfection. Clinical laboratory tests were not significantly changed. Overall, inoculation by a mucosal route produced more prominent disease than did intravenous inoculation. Half of the group I animals were infected with a recombinant infectious clone SARS-CoV derived from the SARS-CoV Urbani strain. This infectious clone produced disease indistinguishable from wild-type Urbani strain.

conclusionsSARS-CoV infection of cynomolgus macaques did not reproduce the severe illness seen in the majority of adult human cases of SARS; however, our results suggest similarities to the milder syndrome of SARS-CoV infection characteristically seen in young children.

Indexed as

Disease Models, AnimalAnimalsAntibody FormationChild, PreschoolFemaleHumansMacaca fascicularisMaleMucous MembraneSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusSeverity of Illness IndexSyndromeVaccinesVirus ReplicationVaccines

Identifiers

PMID16605302
PMCPMC1435788
OpenAlexW2089797630

What OpenQuestion holds

Textmetadata
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.