Evidence map›Paper›PMID 35284643›Full record

ArticleHealth science reports2022

An experimental in silico study on COVID-19: Response of neutrophil-related genes to antibiotics.

Seyyed R Mousavi, Hajie Lotfi, Sharareh Salmanizadeh, Sara Feizbakhshan, Farinaz Khosravian, Maryam S Sajjadi, Sajad R Komachali, Faeze A Beni, Banafshe Torkan, Mohammad Kazemi and 2 more

Open access · goldAbstract read
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Article in Health science reports, 2022. 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
0.8field-weighted citation impact, top 30% 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, 5 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 2 institutions in 1 country.

Seyyed R MousaviCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.ORCID 0000-0001-5389-339X
Hajie LotfiCellular and Molecular Research Center Qazvin University of Medical Sciences Qazvin Iran.ORCID 0000-0001-8450-748X
Sharareh SalmanizadehCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Sara FeizbakhshanCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Farinaz KhosravianCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Maryam S SajjadiMedical Genetics Laboratory Alzahra University Hospital Isfahan University of Medical Sciences Isfahan Iran.
Sajad R KomachaliCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Faeze A BeniCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Banafshe TorkanCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.
Mohammad KazemiDepartment of Genetics and Molecular Biology Isfahan University of Medical Sciences Isfahan Iran.
Ramin SamiDepartment of Pulmonology Isfahan University of Medical Sciences Isfahan Iran.
Mansoor SalehiCellular, Molecular and Genetics Research Center Isfahan University of Medical Sciences Isfahan Iran.ORCID 0000-0002-6565-0907
Isfahan University of Medical Sciences · IRQazvin University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: All components of the immune system are involved in alleviating severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Further research is required to provide detailed insights into COVID-19-related immune compartments and pathways. In addition, a significant percentage of hospitalized COVID-19 patients suspect bacterial infections and antimicrobial resistance occurs following antibiotics treatment. The aim of this study was to evaluate the possible effects of antibiotics on the response of neutrophil-related genes in SARS-CoV-2 patients by an experimental in silico study. Methods: The two data sets GSE1739 and GSE21802 including 10 SARS positive patients and 35 influenza A (H1N1) patients were analyzed, respectively. Differentially expressed genes (DEGs) between these two data sets were determined by GEO2R analysis and the Venn diagram online tool. After determining the hub genes involved in immune responses, the expression of these genes in 30 COVID-19 patients and 30 healthy individuals was analyzed by real-time polymerase chain reaction (PCR). All patients received antibiotics, including levofloxacin, colistin, meropenem, and ceftazidime. Results: GEO2R analysis detected 240 and 120 DEGs in GSE21802 and GSE1739, respectively. Twenty DEGs were considered as enriched hub genes involved in immune processes such as neutrophil degranulation, neutrophil activation, and antimicrobial humoral response. The central nodes were attributed to the genes of neutrophil elastase (ELANE), arginase 1 (ARG-1), lipocalin 2 (LCN2), and defensin 4 (DEFA4). Compared to the healthy subjects, the expression of LCN2 and DEFA4 were significantly reduced in COVID-19 patients. However, no significant differences were observed in the ELANE and AGR-1 levels between COVID-19 subjects and the control group. Conclusions: Activation and degranulation of neutrophils were observed mainly in SARS, and H1N1 infection processes and antibiotics administration could affect neutrophil activity during viral infection. It can be suggested that antibiotics can decrease inflammation by restoring the expression of neutrophil-related genes in COVID-19 patients.

Indexed as

ARG‐1DEFA4ELANELCN2neutrophil‐mediated immunitySARS‐CoV‐2

Identifiers

PMID35284643
PMCPMC8900978
OpenAlexW4220830111

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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.