• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Might SARS-CoV-2 Have Arisen via Serial Passage through an Animal Host or Cell Culture?: A potential explanation for much of the novel coronavirus' distinctive genome.SARS-CoV-2 是否可能通过动物宿主或细胞培养的连续传代而出现?:对新型冠状病毒独特基因组的大部分内容的一种潜在解释。
Bioessays. 2020 Oct;42(10):e2000091. doi: 10.1002/bies.202000091. Epub 2020 Aug 12.
2
Broad and Differential Animal Angiotensin-Converting Enzyme 2 Receptor Usage by SARS-CoV-2.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)对动物血管紧张素转换酶2受体的广泛及差异性利用
J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.00940-20.
3
[Source of the COVID-19 pandemic: ecology and genetics of coronaviruses (Betacoronavirus: Coronaviridae) SARS-CoV, SARS-CoV-2 (subgenus Sarbecovirus), and MERS-CoV (subgenus Merbecovirus).].[新冠疫情的源头:冠状病毒(β冠状病毒:冠状病毒科)、严重急性呼吸综合征冠状病毒(SARS-CoV)、严重急性呼吸综合征冠状病毒2(SARS-CoV-2,Sarbecovirus亚属)和中东呼吸综合征冠状病毒(MERS-CoV,Merbecovirus亚属)的生态学与遗传学。]
Vopr Virusol. 2020;65(2):62-70. doi: 10.36233/0507-4088-2020-65-2-62-70.
4
COVID-19: Time to exonerate the pangolin from the transmission of SARS-CoV-2 to humans.COVID-19:是时候为穿山甲洗脱传播 SARS-CoV-2 给人类的罪名了。
Infect Genet Evol. 2020 Oct;84:104493. doi: 10.1016/j.meegid.2020.104493. Epub 2020 Aug 5.
5
Profile of a killer: the complex biology powering the coronavirus pandemic.杀手剖析:驱动新冠疫情的复杂生物学机制
Nature. 2020 May;581(7806):22-26. doi: 10.1038/d41586-020-01315-7.
6
Enhanced Binding of SARS-CoV-2 Spike Protein to Receptor by Distal Polybasic Cleavage Sites.通过远端多碱性切割位点增强严重急性呼吸综合征冠状病毒2刺突蛋白与受体的结合
ACS Nano. 2020 Aug 25;14(8):10616-10623. doi: 10.1021/acsnano.0c04798. Epub 2020 Aug 4.
7
Structural and functional modelling of SARS-CoV-2 entry in animal models.SARS-CoV-2 入侵动物模型的结构和功能建模。
Sci Rep. 2020 Sep 28;10(1):15917. doi: 10.1038/s41598-020-72528-z.
8
SARS-CoV-2: Zoonotic origin of pandemic coronavirus.严重急性呼吸综合征冠状病毒2:大流行冠状病毒的人畜共患病起源
Acta Virol. 2020;64(3):281-287. doi: 10.4149/av_2020_302.
9
Highly conserved binding region of ACE2 as a receptor for SARS-CoV-2 between humans and mammals.高度保守的 ACE2 结合区域作为人类和哺乳动物之间 SARS-CoV-2 的受体。
Vet Q. 2020 Dec;40(1):243-249. doi: 10.1080/01652176.2020.1823522.
10
Comparison of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein Binding to ACE2 Receptors from Human, Pets, Farm Animals, and Putative Intermediate Hosts.严重急性呼吸综合征冠状病毒 2 刺突蛋白与人、宠物、农场动物和潜在中间宿主 ACE2 受体结合的比较。
J Virol. 2020 Jul 16;94(15). doi: 10.1128/JVI.00831-20.

引用本文的文献

1
Biosafety, biosecurity, and bioethics.生物安全、生物安保和生物伦理。
Monash Bioeth Rev. 2024 Jun;42(1):137-167. doi: 10.1007/s40592-024-00204-3. Epub 2024 Jul 30.
2
Non-uniform aspects of the SARS-CoV-2 intraspecies evolution reopen question of its origin.SARS-CoV-2 种内进化的非均匀性方面再次引发了其起源问题。
Int J Biol Macromol. 2022 Dec 1;222(Pt A):972-993. doi: 10.1016/j.ijbiomac.2022.09.184. Epub 2022 Sep 26.
3
Insertion-and-Deletion Mutations between the Genomes of SARS-CoV, SARS-CoV-2, and Bat Coronavirus RaTG13.刺突蛋白插入缺失突变在 SARS-CoV、SARS-CoV-2 和蝙蝠冠状病毒 RaTG13 之间。
Microbiol Spectr. 2022 Jun 29;10(3):e0071622. doi: 10.1128/spectrum.00716-22. Epub 2022 Jun 6.
4
Thus spoke peptides: SARS-CoV-2 spike gene evolved in humans and then shortly in rats while the rest of its genome in horseshoe bats and then in treeshrews.肽如是说:严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突基因在人类中进化,随后在大鼠中短暂进化,而其基因组的其余部分则先在马蹄蝠中进化,然后在树鼩中进化。
Commun Integr Biol. 2022 Apr 10;15(1):96-104. doi: 10.1080/19420889.2022.2057010. eCollection 2022.
5
Host Manipulation Mechanisms of SARS-CoV-2.SARS-CoV-2 的宿主操纵机制。
Acta Biotheor. 2021 Dec 13;70(1):4. doi: 10.1007/s10441-021-09425-z.
6
There is no "origin" to SARS-CoV-2.SARS-CoV-2 没有“起源”。
Environ Res. 2022 May 1;207:112173. doi: 10.1016/j.envres.2021.112173. Epub 2021 Oct 6.
7
Origin of COVID-19: Dismissing the Mojiang mine theory and the laboratory accident narrative.新冠病毒起源:摒弃“墨江矿洞”及“实验室事故”两种假说。
Environ Res. 2022 Mar;204(Pt B):112141. doi: 10.1016/j.envres.2021.112141. Epub 2021 Sep 28.
8
SARS-CoV-2 Infection: New Molecular, Phylogenetic, and Pathogenetic Insights. Efficacy of Current Vaccines and the Potential Risk of Variants.SARS-CoV-2 感染:新的分子、系统发生和发病机制见解。当前疫苗的功效和变异的潜在风险。
Viruses. 2021 Aug 25;13(9):1687. doi: 10.3390/v13091687.
9
An appeal for an objective, open, and transparent scientific debate about the origin of SARS-CoV-2.呼吁就严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的起源展开一场客观、开放和透明的科学辩论。
Lancet. 2021 Oct 16;398(10309):1402-1404. doi: 10.1016/S0140-6736(21)02019-5. Epub 2021 Sep 17.
10
Can Science Help Resolve the Controversy on the Origins of the SARS-CoV-2 Pandemic?科学能否帮助解决关于 SARS-CoV-2 大流行起源的争议?
mBio. 2021 Aug 31;12(4):e0194821. doi: 10.1128/mBio.01948-21. Epub 2021 Aug 2.

本文引用的文献

1
On the origin and continuing evolution of SARS-CoV-2.关于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的起源及持续进化
Natl Sci Rev. 2020 Jun;7(6):1012-1023. doi: 10.1093/nsr/nwaa036. Epub 2020 Mar 3.
2
Furin: A Potential Therapeutic Target for COVID-19.弗林蛋白酶:新冠病毒病的一个潜在治疗靶点。
iScience. 2020 Oct 23;23(10):101642. doi: 10.1016/j.isci.2020.101642. Epub 2020 Oct 5.
3
Are pangolins the intermediate host of the 2019 novel coronavirus (SARS-CoV-2)?穿山甲是否是 2019 新型冠状病毒(SARS-CoV-2)的中间宿主?
PLoS Pathog. 2020 May 14;16(5):e1008421. doi: 10.1371/journal.ppat.1008421. eCollection 2020 May.
4
A rampage through the body.在体内肆虐。
Science. 2020 Apr 24;368(6489):356-360. doi: 10.1126/science.368.6489.356.
5
The proximal origin of SARS-CoV-2.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的近端起源。
Nat Med. 2020 Apr;26(4):450-452. doi: 10.1038/s41591-020-0820-9.
6
Diarrhea During COVID-19 Infection: Pathogenesis, Epidemiology, Prevention, and Management.新冠病毒感染期间的腹泻:发病机制、流行病学、预防和管理。
Clin Gastroenterol Hepatol. 2020 Jul;18(8):1663-1672. doi: 10.1016/j.cgh.2020.04.001. Epub 2020 Apr 8.
7
Infection and Rapid Transmission of SARS-CoV-2 in Ferrets.雪貂中 SARS-CoV-2 的感染和快速传播。
Cell Host Microbe. 2020 May 13;27(5):704-709.e2. doi: 10.1016/j.chom.2020.03.023. Epub 2020 Apr 6.
8
COVID-19 and the Heart.新型冠状病毒肺炎与心脏
Circ Res. 2020 May 8;126(10):1443-1455. doi: 10.1161/CIRCRESAHA.120.317055. Epub 2020 Apr 7.
9
COVID-19 and the Inpatient Dialysis Unit: Managing Resources during Contingency Planning Pre-Crisis.COVID-19与住院透析单元:危机前应急规划期间的资源管理
Clin J Am Soc Nephrol. 2020 May 7;15(5):720-722. doi: 10.2215/CJN.03750320. Epub 2020 Apr 3.
10
The neuroinvasive potential of SARS-CoV2 may play a role in the respiratory failure of COVID-19 patients.SARS-CoV2 的神经侵袭性可能在 COVID-19 患者的呼吸衰竭中起作用。
J Med Virol. 2020 Jun;92(6):552-555. doi: 10.1002/jmv.25728. Epub 2020 Mar 11.

SARS-CoV-2 是否可能通过动物宿主或细胞培养的连续传代而出现?:对新型冠状病毒独特基因组的大部分内容的一种潜在解释。

Might SARS-CoV-2 Have Arisen via Serial Passage through an Animal Host or Cell Culture?: A potential explanation for much of the novel coronavirus' distinctive genome.

机构信息

Karl Sirotkin LLC, 1301 Tadsworth Terrace, Lake Mary, FL, 32746, USA.

出版信息

Bioessays. 2020 Oct;42(10):e2000091. doi: 10.1002/bies.202000091. Epub 2020 Aug 12.

DOI:10.1002/bies.202000091
PMID:32786014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7435492/
Abstract

Despite claims from prominent scientists that SARS-CoV-2 indubitably emerged naturally, the etiology of this novel coronavirus remains a pressing and open question: Without knowing the true nature of a disease, it is impossible for clinicians to appropriately shape their care, for policy-makers to correctly gauge the nature and extent of the threat, and for the public to appropriately modify their behavior. Unless the intermediate host necessary for completing a natural zoonotic jump is identified, the dual-use gain-of-function research practice of viral serial passage should be considered a viable route by which the novel coronavirus arose. The practice of serial passage mimics a natural zoonotic jump, and offers explanations for SARS-CoV-2's distinctive spike-protein region and its unexpectedly high affinity for angiotensin converting enzyme (ACE2), as well as the notable polybasic furin cleavage site within it. Additional molecular clues raise further questions, all of which warrant full investigation into the novel coronavirus's origins and a re-examination of the risks and rewards of dual-use gain-of-function research.

摘要

尽管一些知名科学家声称新型冠状病毒(SARS-CoV-2)无疑是自然产生的,但这种新型冠状病毒的病因仍然是一个紧迫且尚未解决的问题:如果不知道疾病的真正性质,临床医生就不可能正确地调整他们的治疗方案,政策制定者也无法正确评估威胁的性质和程度,公众也无法适当地改变他们的行为。除非确定了完成自然人畜共患病跳跃所必需的中间宿主,否则应该将病毒连续传代的两用增益功能研究实践视为新型冠状病毒出现的一种可行途径。连续传代的做法模拟了自然人畜共患病跳跃,并解释了为什么 SARS-CoV-2 的独特刺突蛋白区域及其对血管紧张素转化酶(ACE2)的意外高亲和力,以及其中明显的多碱性弗林裂解位点。其他分子线索提出了更多问题,所有这些都需要对新型冠状病毒的起源进行全面调查,并重新审视两用增益功能研究的风险和回报。