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在感染两种新冠病毒变体的人类鼻上皮细胞中检测到的早期从头编程“CoV-MAC-TED”主要复杂性状有望帮助设计治疗策略。

Major Complex Trait for Early De Novo Programming 'CoV-MAC-TED' Detected in Human Nasal Epithelial Cells Infected by Two SARS-CoV-2 Variants Is Promising to Help in Designing Therapeutic Strategies.

作者信息

Costa José Hélio, Aziz Shahid, Noceda Carlos, Arnholdt-Schmitt Birgit

机构信息

Functional Genomics and Bioinformatics Group, Department of Biochemistry and Molecular Biology, Federal University of Ceará, Fortaleza 60451-970, Brazil.

Non-Institutional Competence Focus (NICFocus) 'Functional Cell Reprogramming and Organism Plasticity' (FunCROP), Coordinated from Foros de Vale de Figueira, 7050-704 Montemor-o-Novo, Portugal.

出版信息

Vaccines (Basel). 2021 Nov 26;9(12):1399. doi: 10.3390/vaccines9121399.

Abstract

BACKGROUND

Early metabolic reorganization was only recently recognized as an essentially integrated part of immunology. In this context, unbalanced ROS/RNS levels connected to increased aerobic fermentation, which is linked to alpha-tubulin-based cell restructuring and control of cell cycle progression, were identified as a major complex trait for early de novo programming ('CoV-MAC-TED') during SARS-CoV-2 infection. This trait was highlighted as a critical target for developing early anti-viral/anti-SARS-CoV-2 strategies. To obtain this result, analyses had been performed on transcriptome data from diverse experimental cell systems. A call was released for wide data collection of the defined set of genes for transcriptome analyses, named 'ReprogVirus', which should be based on strictly standardized protocols and data entry from diverse virus types and variants into the 'ReprogVirus Platform'. This platform is currently under development. However, so far, an in vitro cell system from primary target cells for virus attacks that could ideally serve for standardizing the data collection of early SARS-CoV-2 infection responses has not been defined.

RESULTS

Here, we demonstrate transcriptome-level profiles of the most critical 'ReprogVirus' gene sets for identifying 'CoV-MAC-TED' in cultured human nasal epithelial cells infected by two SARS-CoV-2 variants differing in disease severity. Our results (a) validate 'Cov-MAC-TED' as a crucial trait for early SARS-CoV-2 reprogramming for the tested virus variants and (b) demonstrate its relevance in cultured human nasal epithelial cells.

CONCLUSION

In vitro-cultured human nasal epithelial cells proved to be appropriate for standardized transcriptome data collection in the 'ReprogVirus Platform'. Thus, this cell system is highly promising to advance integrative data analyses with the help of artificial intelligence methodologies for designing anti-SARS-CoV-2 strategies.

摘要

背景

早期代谢重组直到最近才被视为免疫学中一个基本的整合部分。在这种情况下,与有氧发酵增加相关的活性氧/氮化物(ROS/RNS)水平失衡,这与基于α-微管蛋白的细胞重组和细胞周期进程控制有关,被确定为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染期间早期从头编程(“CoV-MAC-TED”)的一个主要复杂特征。这一特征被强调为开发早期抗病毒/SARS-CoV-2策略的关键靶点。为了获得这一结果,已对来自不同实验细胞系统的转录组数据进行了分析。呼吁广泛收集用于转录组分析的一组定义基因的数据,即“ReprogVirus”,该数据应基于严格标准化的方案以及将来自不同病毒类型和变体的数据输入“ReprogVirus平台”。该平台目前正在开发中。然而,到目前为止,尚未确定一种来自病毒攻击主要靶细胞的体外细胞系统,该系统理想情况下可用于标准化早期SARS-CoV-2感染反应的数据收集。

结果

在这里,我们展示了在感染两种疾病严重程度不同的SARS-CoV-2变体的培养人鼻上皮细胞中,用于识别“CoV-MAC-TED”的最关键“ReprogVirus”基因集的转录组水平概况。我们的结果(a)验证了“Cov-MAC-TED”是测试病毒变体早期SARS-CoV-2重编程的关键特征,并且(b)证明了其在培养的人鼻上皮细胞中的相关性。

结论

体外培养的人鼻上皮细胞被证明适用于“ReprogVirus平台”的标准化转录组数据收集。因此,该细胞系统在借助人工智能方法推进综合数据分析以设计抗SARS-CoV-2策略方面极具前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e9/8708361/82bc9442b223/vaccines-09-01399-g001.jpg

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