Evidence map›Paper›PMID 35062231›Full record

ArticleViruses2021

SARS-CoV-2 Variants of Concern Infect the Respiratory Tract and Induce Inflammatory Response in Wild-Type Laboratory Mice.

Shannon Stone, Hussin Alwan Rothan, Janhavi Prasad Natekar, Pratima Kumari, Shaligram Sharma, Heather Pathak, Komal Arora, Tabassum Tasnim Auroni, Mukesh Kumar

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

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  5. SARS-CoV-2 XBB.1.5 infects wild-type C57BL/6 mice and induces a protective CD4Frontiers in cellular and infection microbiology · 2025
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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

9 authors at 1 institution in 1 country.

Shannon StoneDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.
Hussin Alwan RothanDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.ORCID 0000-0002-7300-6388
Janhavi Prasad NatekarDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.ORCID 0000-0003-0340-082X
Pratima KumariDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.
Shaligram SharmaDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.ORCID 0000-0001-9719-7572
Heather PathakDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.
Komal AroraDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.
Tabassum Tasnim AuroniDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.
Mukesh KumarDepartment of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30303, USA.ORCID 0000-0003-0970-4875
Georgia State University · US

Funding

A Guinea Pig Model of Zika Virus DiseaseR21OD024896 · OD · UNIVERSITY OF HAWAII AT MANOA · PI KUMAR, MUKESH · 2017 to 2018
$402k
NIH HHS R21 OD024896
6 · The paper itself

Abstract

The emergence of new severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants of concern pose a major threat to public health, due to possible enhanced virulence, transmissibility and immune escape. These variants may also adapt to new hosts, in part through mutations in the spike protein. In this study, we evaluated the infectivity and pathogenicity of SARS-CoV-2 variants of concern in wild-type C57BL/6 mice. Six-week-old mice were inoculated intranasally with a representative virus from the original B.1 lineage, or the emerging B.1.1.7 and B.1.351 lineages. We also infected a group of mice with a mouse-adapted SARS-CoV-2 (MA10). Viral load and mRNA levels of multiple cytokines and chemokines were analyzed in the lung tissues on day 3 after infection. Our data show that unlike the B.1 virus, the B.1.1.7 and B.1.351 viruses are capable of infecting C57BL/6 mice and replicating at high concentrations in the lungs. The B.1.351 virus replicated to higher titers in the lungs compared with the B.1.1.7 and MA10 viruses. The levels of cytokines (IL-6, TNF-α, IL-1β) and chemokine (CCL2) were upregulated in response to the B.1.1.7 and B.1.351 infection in the lungs. In addition, robust expression of viral nucleocapsid protein and histopathological changes were detected in the lungs of B.1.351-infected mice. Overall, these data indicate a greater potential for infectivity and adaptation to new hosts by emerging SARS-CoV-2 variants.

Indexed as

AnimalsCOVID-19CytokinesDisease Models, AnimalHost SpecificityInflammationLungMiceMice, Inbred C57BLSARS-CoV-2Viral LoadVirus ReplicationCytokinesC57BL/6 miceCOVID-19host-rangeinflammationSARS-CoV-2 variants

Identifiers

PMID35062231
PMCPMC8777867
OpenAlexW4225358271

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.