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2
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Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant.德尔塔刺突 P681R 突变增强了 SARS-CoV-2 对阿尔法变体的适应能力。
Cell Rep. 2022 May 17;39(7):110829. doi: 10.1016/j.celrep.2022.110829. Epub 2022 Apr 29.
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Proteolytic activation of SARS-CoV-2 spike protein.SARS-CoV-2 刺突蛋白的蛋白水解激活。
Microbiol Immunol. 2022 Jan;66(1):15-23. doi: 10.1111/1348-0421.12945. Epub 2021 Oct 12.
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Lectins enhance SARS-CoV-2 infection and influence neutralizing antibodies.凝集素增强 SARS-CoV-2 感染并影响中和抗体。
Nature. 2021 Oct;598(7880):342-347. doi: 10.1038/s41586-021-03925-1. Epub 2021 Aug 31.
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SARS-CoV-2 spike and its adaptable furin cleavage site.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白及其适应性弗林蛋白酶切割位点
Lancet Microbe. 2021 Oct;2(10):e488-e489. doi: 10.1016/S2666-5247(21)00174-9. Epub 2021 Aug 6.
5
Acquisition of the L452R Mutation in the ACE2-Binding Interface of Spike Protein Triggers Recent Massive Expansion of SARS-CoV-2 Variants.刺突蛋白 ACE2 结合界面 L452R 突变的获得引发了 SARS-CoV-2 变体的近期大规模扩张。
J Clin Microbiol. 2021 Oct 19;59(11):e0092121. doi: 10.1128/JCM.00921-21. Epub 2021 Aug 11.
6
SARS-CoV-2 Spike Mutations, L452R, T478K, E484Q and P681R, in the Second Wave of COVID-19 in Maharashtra, India.印度马哈拉施特拉邦第二波新冠疫情中出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白突变,L452R、T478K、E484Q和P681R
Microorganisms. 2021 Jul 20;9(7):1542. doi: 10.3390/microorganisms9071542.
7
SARS-CoV-2 variant B.1.617 is resistant to bamlanivimab and evades antibodies induced by infection and vaccination.SARS-CoV-2 变体 B.1.617 对巴美洛单抗具有耐药性,并能逃避由感染和接种疫苗引起的抗体。
Cell Rep. 2021 Jul 20;36(3):109415. doi: 10.1016/j.celrep.2021.109415. Epub 2021 Jun 29.
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A human three-dimensional neural-perivascular 'assembloid' promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology.人源三维神经血管“聚集物”促进星形胶质细胞发育并可模拟 SARS-CoV-2 神经病理学。
Nat Med. 2021 Sep;27(9):1600-1606. doi: 10.1038/s41591-021-01443-1. Epub 2021 Jul 9.
9
Reduced sensitivity of SARS-CoV-2 variant Delta to antibody neutralization.德尔塔变异株对抗体中和的敏感性降低。
Nature. 2021 Aug;596(7871):276-280. doi: 10.1038/s41586-021-03777-9. Epub 2021 Jul 8.
10
Infection and Vaccine-Induced Neutralizing-Antibody Responses to the SARS-CoV-2 B.1.617 Variants.针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)B.1.617变体的感染及疫苗诱导的中和抗体反应
N Engl J Med. 2021 Aug 12;385(7):664-666. doi: 10.1056/NEJMc2107799. Epub 2021 Jul 7.

SARS-CoV-2 和大流行潜力 RNA 病毒的神经病理生理学:比较分析。

Neurological pathophysiology of SARS-CoV-2 and pandemic potential RNA viruses: a comparative analysis.

机构信息

Department of Epidemiology, University of California, Los Angeles, CA, USA.

Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA, USA.

出版信息

FEBS Lett. 2021 Dec;595(23):2854-2871. doi: 10.1002/1873-3468.14227. Epub 2021 Nov 22.

DOI:10.1002/1873-3468.14227
PMID:34757622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8652524/
Abstract

SARS-CoV-2 has infected hundreds of millions of people with over four million dead, resulting in one of the worst global pandemics in recent history. Neurological symptoms associated with COVID-19 include anosmia, ageusia, headaches, confusion, delirium, and strokes. These may manifest due to viral entry into the central nervous system (CNS) through the blood-brain barrier (BBB) by means of ill-defined mechanisms. Here, we summarize the abilities of SARS-CoV-2 and other neurotropic RNA viruses, including Zika virus and Nipah virus, to cross the BBB into the CNS, highlighting the role of magnetic resonance imaging (MRI) in assessing presence and severity of brain structural changes in COVID-19 patients. We present new insight into key mutations in SARS-CoV-2 variants B.1.1.7 (P681H) and B.1.617.2 (P681R), which may impact on neuropilin 1 (NRP1) binding and CNS invasion. We postulate that SARS-CoV-2 may infect both peripheral cells capable of crossing the BBB and brain endothelial cells to traverse the BBB and spread into the brain. COVID-19 patients can be followed up with MRI modalities to better understand the long-term effects of COVID-19 on the brain.

摘要

SARS-CoV-2 已感染数亿人,导致超过 400 万人死亡,是近代历史上最严重的全球大流行之一。与 COVID-19 相关的神经系统症状包括嗅觉丧失、味觉丧失、头痛、意识混乱、谵妄和中风。这些症状可能是由于病毒通过血脑屏障 (BBB) 进入中枢神经系统 (CNS),其进入机制尚不清楚。在这里,我们总结了 SARS-CoV-2 和其他神经营养性 RNA 病毒(包括寨卡病毒和尼帕病毒)穿过血脑屏障进入中枢神经系统的能力,强调了磁共振成像 (MRI) 在评估 COVID-19 患者大脑结构变化的存在和严重程度方面的作用。我们提出了 SARS-CoV-2 变体 B.1.1.7 (P681H) 和 B.1.617.2 (P681R) 中关键突变的新见解,这些突变可能影响神经纤毛蛋白 1 (NRP1) 的结合和中枢神经系统入侵。我们推测,SARS-CoV-2 可能感染能够穿过血脑屏障的外周细胞和脑内皮细胞,从而穿过血脑屏障并传播到大脑。可以使用 MRI 方式对 COVID-19 患者进行随访,以更好地了解 COVID-19 对大脑的长期影响。