Evidence map›Paper›PMID 34514445›Full record

ArticleBrain disorders (Amsterdam, Netherlands)2021

DJ-1-Nrf2 axis is activated upon murine β-coronavirus infection in the CNS.

Soumya Kundu, Fareeha Saadi, Sourodip Sengupta, Gisha Rose Antony, Vineeth A Raveendran, Rahul Kumar, Mithila Ashok Kamble, Lucky Sarkar, Amy Burrows, Debnath Pal and 2 more

Open access · goldAbstract read
In one paragraph

Article in Brain disorders (Amsterdam, Netherlands), 2021. 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
0.6field-weighted citation impact, top 28% 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, 6 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

12 authors at 3 institutions in 2 countries.

Soumya KunduDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Fareeha SaadiDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Sourodip SenguptaDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Gisha Rose AntonyDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Vineeth A RaveendranDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Rahul KumarDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Mithila Ashok KambleDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Lucky SarkarDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Amy BurrowsDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Ohio, USA.
Debnath PalDepartment of Computational and Data Sciences, Indian Institute of Science, Bangalore, India.
Ganes C SenDepartment of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Ohio, USA.
Jayasri Das SarmaDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, West Bengal, India.
Indian Institute of Science Education and Research Kolkata · INCleveland Clinic Lerner College of Medicine · USIndian Institute of Science Bangalore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronaviruses have emerged as alarming pathogens owing to their inherent ability of genetic variation and cross-species transmission. Coronavirus infection burdens the endoplasmic reticulum (ER.), causes reactive oxygen species production and induces host stress responses, including unfolded protein response (UPR) and antioxidant system. In this study, we have employed a neurotropic murine β-coronavirus (M-CoV) infection in the Central Nervous System (CNS) of experimental mice model to study the role of host stress responses mediated by interplay of DJ-1 and XBP1. DJ-1 is an antioxidant molecule with established functions in neurodegeneration. However, its regulation in virus-induced cellular stress response is less explored. Our study showed that M-CoV infection activated the glial cells and induced antioxidant and UPR genes during the acute stage when the viral titer peaks. As the virus particles decreased and acute neuroinflammation diminished at day ten p.i., a significant up-regulation in UPR responsive XBP1, antioxidant DJ-1, and downstream signaling molecules, including Nrf2, was recorded in the brain tissues. Additionally, preliminary in silico analysis of the binding between the DJ-1 promoter and a positively charged groove of XBP1 is also investigated, thus hinting at a mechanism behind the upregulation of DJ-1 during MHV-infection. The current study thus attempts to elucidate a novel interplay between the antioxidant system and UPR in the outcome of coronavirus infection.

Indexed as

AstrocyteMicrogliaMouse Hepatitis VirusNeuro-COVIDOxidative stressXBP1-DJ-1-Nrf2 axis

Identifiers

PMID34514445
PMCPMC8418700
OpenAlexW3197026699

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.