Geographic Classification and Identification of SARS-CoV2 From Related Viral Sequences

Q4 Biochemistry, Genetics and Molecular Biology International Journal of Biology and Biomedical Engineering Pub Date : 2021-07-19 DOI:10.46300/91011.2021.15.31
F. F. Sherif, K. Ahmed
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引用次数: 1

Abstract

The COVID-19 pandemic has introduced to mild the risks of deadly epidemic-prone illnesses sweeping our globalized planet. The pandemic is still going strong, with additional viral variations popping up all the time. For the close to future, the international response will have to continue. The molecular tests for SARS-CoV-2 detection may lead to False-negative results due to their genetic similarity with other coronaviruses, as well as their ability to mutate and evolve. Furthermore, the clinical features caused by SARS-CoV-2 seem to be like the symptoms of other viral infections, making identification even harder. We constructed seven hidden Markov models for each coronavirus family (SARS-CoV2, HCoV-OC43, HCoV-229E, HCoV-NL63, HCoV-HKU1, MERS-CoV, and SARS-CoV), using their complete genome to accurate diagnose human infections. Besides, this study characterized and classified the SARS-CoV2 strains according to their different geographical regions. We built six SARS-CoV2 classifiers for each world's continent (Africa, Asia, Europe, North America, South America, and Australia). The dataset used was retrieved from the NCBI virus database. The classification accuracy of these models achieves 100% in differentiating any virus model among others in the Coronavirus family. However, the accuracy of the continent models showed a variable range of accuracies, sensitivity, and specificity due to heterogeneous evolutional paths among strains from 27 countries. South America model was the highest accurate model compared to the other geographical models. This finding has vital implications for the management of COVID-19 and the improvement of vaccines.
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从相关病毒序列中对严重急性呼吸系统综合征冠状病毒2型的地理分类和鉴定
新冠肺炎大流行降低了席卷全球的致命流行病的风险。新冠疫情仍在持续,不断出现额外的病毒变异。在不久的将来,国际社会必须继续作出反应。严重急性呼吸系统综合征冠状病毒2型检测的分子测试可能会导致假阴性结果,因为它们与其他冠状病毒的基因相似,并且具有变异和进化的能力。此外,严重急性呼吸系统综合征冠状病毒2型引起的临床特征似乎与其他病毒感染的症状相似,这使得识别更加困难。我们为每个冠状病毒家族(严重急性呼吸系统综合征冠状病毒2型、冠状病毒OC43型、冠状病毒229E型、冠状病毒NL63型、冠状病毒HKU1型、MERS-CoV型和非典型肺炎冠状病毒)构建了七个隐马尔可夫模型,使用它们的全基因组准确诊断人类感染。此外,本研究还根据不同的地理区域对严重急性呼吸系统综合征冠状病毒2型菌株进行了表征和分类。我们为每个世界大陆(非洲、亚洲、欧洲、北美、南美和澳大利亚)建立了六个严重急性呼吸系统综合征冠状病毒2型分类器。使用的数据集是从NCBI病毒数据库中检索的。这些模型的分类准确率在区分冠状病毒家族中的任何病毒模型时达到100%。然而,由于来自27个国家的菌株之间的异质进化路径,大陆模型的准确性显示出不同的准确性、敏感性和特异性。与其他地理模型相比,南美洲模型是准确度最高的模型。这一发现对新冠肺炎的管理和疫苗的改进具有重要意义。
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来源期刊
International Journal of Biology and Biomedical Engineering
International Journal of Biology and Biomedical Engineering Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
自引率
0.00%
发文量
42
期刊介绍: Topics: Molecular Dynamics, Biochemistry, Biophysics, Quantum Chemistry, Molecular Biology, Cell Biology, Immunology, Neurophysiology, Genetics, Population Dynamics, Dynamics of Diseases, Bioecology, Epidemiology, Social Dynamics, PhotoBiology, PhotoChemistry, Plant Biology, Microbiology, Immunology, Bioinformatics, Signal Transduction, Environmental Systems, Psychological and Cognitive Systems, Pattern Formation, Evolution, Game Theory and Adaptive Dynamics, Bioengineering, Biotechnolgies, Medical Imaging, Medical Signal Processing, Feedback Control in Biology and Chemistry, Fluid Mechanics and Applications in Biomedicine, Space Medicine and Biology, Nuclear Biology and Medicine.
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