Evidence map›Paper›PMID 33295839›Full record

ArticleEmerging microbes & infections2020

An infectious cDNA clone of a growth attenuated Korean isolate of MERS coronavirus KNIH002 in clade B.

Minwoo Kim, Hee Cho, Seung-Hoon Lee, Woo-Jung Park, Jeong-Min Kim, Jae-Su Moon, Geon-Woo Kim, Wooseong Lee, Hae-Gwang Jung, Jeong-Sun Yang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 9 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

14 authors at 4 institutions in 1 country.

Minwoo KimDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Hee ChoDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Seung-Hoon LeeDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Woo-Jung ParkDivision of Emerging Infectious Disease and Vector Research, Center for Infectious Diseases Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Kore.
Jeong-Min KimDivision of Viral Diseases, Center for Laboratory Control of Infectious Diseases, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Korea.
Jae-Su MoonDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Geon-Woo KimDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Wooseong LeeDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Hae-Gwang JungDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Jeong-Sun YangDivision of Emerging Infectious Disease and Vector Research, Center for Infectious Diseases Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Kore.
Jang-Hoon ChoiDivision of Viral Disease Research, Center for Infectious Diseases Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Korea.
Joo-Yeon LeeDivision of Emerging Infectious Disease and Vector Research, Center for Infectious Diseases Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Kore.
Sung Soon KimCenter for Infectious Diseases Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Republic of Korea.
Jong-Won OhDepartment of Biotechnology, Yonsei University, Seoul, Korea.
Yonsei University · KRKorea Center for Disease Control and Prevention · KRKorea Disease Control and Prevention Agency · KRKorea National Institute of Health · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MERS-CoV isolated during the 2015 nosocomial outbreak in Korea showed distinctive differences in mortality and transmission patterns compared to the prototype MERS-CoV EMC strain belonging to clade A. We established a BAC-based reverse genetics system for a Korean isolate of MERS-CoV KNIH002 in the clade B phylogenetically far from the EMC strain, and generated a recombinant MERS-CoV expressing red fluorescent protein. The virus rescued from the infectious clone and KNIH002 strain displayed growth attenuation compared to the EMC strain. Consecutive passages of the rescued virus rapidly generated various ORF5 variants, highlighting its genetic instability and calling for caution in the use of repeatedly passaged virus in pathogenesis studies and for evaluation of control measures against MERS-CoV. The infectious clone for the KNIH002 in contemporary epidemic clade B would be useful for better understanding of a functional link between molecular evolution and pathophysiology of MERS-CoV by comparative studies with EMC strain.

Indexed as

AnimalsCell Line, TumorChlorocebus aethiopsClone CellsCricetinaeDNA, ComplementaryHumansMiddle East Respiratory Syndrome CoronavirusReceptors, VirusVero CellsViral ProteinsDNA, ComplementaryReceptors, VirusViral Proteinsclade B Korean isolategrowth attenuationinfectious cDNA cloneMERS-CoVORF5 deletion variants

Identifiers

PMID33295839
PMCPMC7782039
OpenAlexW3112052597

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.