Evidence map›Paper›PMID 36005818›Full record

ArticleMicrobiology spectrum2022

Immunological and Pathological Peculiarity of Severe Acute Respiratory Syndrome Coronavirus 2 Beta Variant.

Sunhee Lee, Gun Young Yoon, Su Jin Lee, Young-Chan Kwon, Hyun Woo Moon, Yu-Jin Kim, Haesoo Kim, Wooseong Lee, Gi Uk Jeong, Chonsaeng Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 11 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

13 authors at 2 institutions in 1 country.

Sunhee Lee *Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Gun Young Yoon *Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Su Jin Lee *Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Young-Chan KwonCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.ORCID 0000-0003-1100-5168
Hyun Woo MoonCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Yu-Jin KimCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Haesoo KimCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Wooseong LeeCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Gi Uk JeongCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Chonsaeng KimCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Kyun-Do KimCenter for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Seong-Jun Kim *Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.
Dae-Gyun Ahn *Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technologygrid.29869.3c, Daejeon, South Korea.ORCID 0000-0001-8251-8820
Korea Research Institute of Chemical Technology · KRKonkuk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diverse severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants have emerged since the beginning of the COVID-19 pandemic. We investigated the immunological and pathological peculiarity of the SARS-CoV-2 beta variant of concern (VoC) compared to the ancestral strain. Comparative analysis of phenotype and pathology revealed that the beta VoC induces slower disease progression and a prolonged presymptomatic period in the early stages of SARS-CoV-2 infection but ultimately causes sudden death in the late stages of infection in the K18-hACE2 mouse model. The beta VoC induced enhanced activation of CXCL1/2-CXCR2-NLRP3-IL-1β signal cascade accelerating neutrophil recruitment and lung pathology in beta variant-infected mice, as evidenced by multiple analyses of SARS-CoV-2-induced inflammatory cytokines and transcriptomes. CCL2 was one of the most highly secreted cytokines in the early stages of infection. Its blockade reduced virus-induced weight loss and delayed mortality. Our study provides a better understanding of the variant characteristics and need for treatment.

Indexed as

COVID-19SARS-CoV-2AnimalsCytokinesDisease Models, AnimalHumansInterleukin-1betaMiceNLR Family, Pyrin Domain-Containing 3 ProteinPandemicsCytokinesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinCOVID-19cytokineSARS-CoV-2transcriptomevariant

Identifiers

PMID36005818
PMCPMC9602775
OpenAlexW4293091736

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.