In silico and experimental analysis of ribosomal proteins expressions in SARS-cov-2 patients.

IF 3.3 3区 医学 Q3 IMMUNOLOGY
Microbial pathogenesis Pub Date : 2025-09-01 Epub Date: 2025-06-19 DOI:10.1016/j.micpath.2025.107814
Farnaz Vafanezhad, Shiva Ansari Astaneh, Zahra Rashvand, Nematollah Gheibi, Seyyed Reza Mousavi, Ali Abdi, Azam Janati Esfahani, Hossein Ahmadpour-Yazdi, Hajie Lotfi
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Abstract

The expression levels of ribosomal proteins (RPs), selected based on microarray data, were analyzed in severe and mild infected patients with SARS-CoV-2 virus. qRT-PCR (Quantitative reverse transcription polymerase chain reaction) was performed to measure gene expression levels. Significant down-regulation was observed in RPL27a (-0.75 ± 2.95 in severe vs. -1.71 ± 1.91 in mild), RPL26 (0.021 ± 2.12 in severe vs. -1.23 ± 2.06 in mild), and RPL14 (-1.51 ± 1.9 in severe vs. -0.79 ± 1.5 in mild) (P < 0.05). On the other hand, no significant differences were found in the expression of RPL23 (-1.6 ± 3.4 in severe vs. -2.0 ± 2.69 in mild) and RPL31 (-2.5 ± 1.77 in severe vs. -2.09 ± 2.41 in mild). A significant correlation was identified between RPL26, RPL14, and RPL27a in mild patients, while RPL23 correlated with RPL31 and RPL27a in severe patients. These findings confirm the involvement of ribosomal proteins in SARS-CoV-2 infections in both severe and mild cases, suggesting their influence on the severity of the disease.

SARS-CoV-2患者核糖体蛋白表达的计算机和实验分析。
分析了基于微阵列数据选择的核糖体蛋白(RPs)在重症和轻度SARS-CoV-2病毒感染患者中的表达水平。采用定量逆转录聚合酶链反应(qRT-PCR)检测基因表达水平。RPL27a(重度组为-0.75±2.95,轻度组为-1.71±1.91)、RPL26(重度组为- 0.021±2.12,轻度组为-1.23±2.06)、RPL14(重度组为-1.51±1.9,轻度组为-0.79±1.5)显著下调(P< 0.05)。RPL23(严重组-1.6±3.4比轻度组-2.0±2.69)和RPL31(严重组-2.5±1.77比轻度组-2.09±2.41)的表达差异无统计学意义。轻度患者的RPL26、RPL14和RPL27a存在显著相关性,重度患者的RPL23与RPL31和RPL27a存在显著相关性。这些发现证实了核糖体蛋白参与了严重和轻度SARS-CoV-2感染,表明它们对疾病严重程度的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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