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Evaluation of lncRNA EGOT and ISG15 expression in SARSCoV-2 infection

سال انتشار: 1401
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 211
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شناسه ملی سند علمی:

MEDISM23_079

تاریخ نمایه سازی: 16 مهر 1401

چکیده مقاله Evaluation of lncRNA EGOT and ISG15 expression in SARSCoV-2 infection

Background and Aim : The recent coronavirus disease 2019 (COVID-19) pandemic, caused bysevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), activates antiviral immuneresponses and uncontrolled inflammatory reactions. Recent studies have demonstrated that longnoncoding RNAs (lncRNAs) which are a class of non-coding RNAs with more than 200nucleotides in length, have various biological functions and participate in the regulation ofimmunity signaling pathways in viral infections. Several investigations have indicated the lncRNAEosinophil Granule Ontogeny Transcript (EGOT) levels can be up-regulated in SARS-CoV-2infection. The NF-κB pathway is EGOT inducer and therefore, EGOT takes part as a negativeregulator in the type I interferon response. On the other hand, the interferon I immunity responseand ISG15 expression level can be increased by EGOT depletion. The same pattern is alsoobserved in other viral infections, such as HCV chronic infection. This present survey aimed toassess the blood levels of EGOT and ISG15 lncRNAs in COVID-19 patients in comparison withhealthy controls.Methods : In this case-control study, blood samples were collected from 14 COVID-19 patientsin comparison with 14 healthy controls who were enrolled at Taleghani Hospital, Shahid BeheshtiUniversity of Medical Science. Total RNA was isolated by RiboEX™ total RNA extractionsolution (GeneAll, Seoul, South Korea). After cDNA synthesis, quantitative real-time PCR wasused to detect levels of EGOT and ISG15. Expression levels were assessed using the GraphPadPrism software through the 2-ΔΔCt method.Results : The result indicates that the gene expression level of EGOT in SARS-CoV-2 infectedpatients is up-regulated compared to the control group (Fold change=11.073), but the oppositeresult has been observed for ISG15 expression level and it was down-regulated (Foldchange=0.2217). A significant difference was found in blood levels of EGOT and ISG15 betweenpatients and control group (P values 0.0383 and 0.0053, respectively).Conclusion : According to these results, there is a correlation between EGOT and ISG15expression levels and SARS-CoV-2 infection. Also, increased level of EGOT acts as a negativeregulator of interferon I immunity response by blocking the expression of ISG15 and other ISGswhich can lead to promoting viral replication. It seems EGOT lncRNA can be a useful keytherapeutic target for the treatment of COVID-19 patients.

کلیدواژه های Evaluation of lncRNA EGOT and ISG15 expression in SARSCoV-2 infection:

نویسندگان مقاله Evaluation of lncRNA EGOT and ISG15 expression in SARSCoV-2 infection

Zahra Sefatjoo

Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran -Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroente

Seyed Reza Mohebbi

Research Center for Gastroenterology and Liver Diseases, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Seyed Masoud Hosseini

Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran

Sharzad Shoraka

Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran -Department of Microbiology and Microbial Biotechnolog

Shabnam Kazemian

Research Center for Gastroenterology and Liver Diseases, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Mahsa Saeedi Niasar

Research Center for Gastroenterology and Liver Diseases, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran