Sars-Cov-2和Ace -2突变谱可改变传染性、免疫原性和疾病严重程度

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由于其对呼吸系统的潜在破坏性影响,它被称为SARS- COV 2(严重急性呼吸综合征冠状病毒2)。然而,该疾病的严重程度因地理区域和受感染人群的病毒载量而异。最近的研究表明,病毒在刺突蛋白上获得了几个突变,刺突蛋白是病毒颗粒的受体结合域。这些突变也改变了病毒包膜的糖基化模式。突变还会使刺突蛋白的S1和S1结构域发生不同的糖基化,从而通过改变与ACE2受体结合的可能性来调节其传染性。传染性的改变也可能改变疾病的免疫原性和表现谱。ACE 2受体突变位点也扰乱了糖基化模式,从而改变了与病毒的结合能力。所有这些突变都可能潜在地改变世界范围内报道的疾病严重程度。因此,SARS-CoV 2和ACE2受体的突变联合或单独调节整个疾病情景,这是COVID研究中最感兴趣的部分。在这篇综述中,我们将揭示COVID -19疾病谱的这些领域。
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Mutational Spectra of Sars-Cov-2 And Ace 2 Can Modify Infectivity, Immunogenicity and Disease Severity: A Review
COVID 19 is primarily characterized as severe respiratory syndrome, careful review revealed that it has multisystem involvement (Mao et al 2020). Due to its potentially damaging effects on respiratory system it is termed as SARS- COV 2 (severe acute respiratory syndrome corona virus 2). However, severity of the disease differentially changes from one to another geographical area and on the viral load of people affected. It has been shown from recent studies that the virus acquired several mutations on the spike protein which is the receptor binding domain of the virus particle. These mutations also alter the glycosylation pattern of the viral envelop. Mutation also differentially glycosylate the S1 and S1 domain of the spike protein and thereby modulate its infectivity through changes the potentiality of binding with ACE2 receptor. Changes in infectivity may also alter immunogenicity and manifestation spectra of the disease. ACE 2 receptor mutation site also perturb the glycosylation pattern and therefore alters the binding capacity with virus. All these mutations may potentially alter disease severity which is reported worldwide. Mutation of SARS-CoV 2 and ACE2 receptor in combination or in alone therefore modulate the entire picture of disease scenario which is the most interested part of COVID research. In this review we are going to unrevealing these areas of COVID -19 disease spectra.
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