一种不依赖ACE2-和dpp4进入细胞的蝙蝠merbecv的体内外特性

IF 3.8 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2025-07-22 Epub Date: 2025-06-17 DOI:10.1128/jvi.00727-25
Hiromichi Matsugo, Tomoya Kitamura, Naohiro Takahashi, James Chambers, Ayano Ichikawa, Misa Katayama, Kaixin Li, Wataru Sekine, Kosuke Ohira, Hiroho Ishida, Akiko Takenaka-Uema, Kazuyuki Uchida, Masayuki Shimojima, Taisuke Horimoto, Shin Murakami
{"title":"一种不依赖ACE2-和dpp4进入细胞的蝙蝠merbecv的体内外特性","authors":"Hiromichi Matsugo, Tomoya Kitamura, Naohiro Takahashi, James Chambers, Ayano Ichikawa, Misa Katayama, Kaixin Li, Wataru Sekine, Kosuke Ohira, Hiroho Ishida, Akiko Takenaka-Uema, Kazuyuki Uchida, Masayuki Shimojima, Taisuke Horimoto, Shin Murakami","doi":"10.1128/jvi.00727-25","DOIUrl":null,"url":null,"abstract":"<p><p>Betacoronaviruses, which have caused three human outbreaks within the last two decades, are thought to originate from bats, raising the concern that bat coronaviruses could cause a novel human outbreak in the future. To determine whether the bat merbecovirus EjCoV-3 strain, previously detected in <i>Eptesicus japonensis</i> in Japan, has the potential to infect humans, we analyzed its cellular entry mechanism. Cellular entry of EjCoV-3 via the spike protein requires protease treatment and is mediated by an unknown receptor, other than DPP4 or ACE2. We generated cultivable recombinant EjCoV-3 using bacterial artificial chromosome-based reverse genetics and found that it efficiently replicated in human respiratory and intestinal cell cultures as well as nasal ciliated epithelium in hamsters. These findings suggest that bat merbecovirus with ACE2- and DPP4-independent cell entry has the potential to cause human infections, highlighting the importance of extensive bat surveillance for pandemic preparedness.</p><p><strong>Importance: </strong>Betacoronaviruses, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and SARS-CoV-2, have caused three significant outbreaks in the past two decades and are believed to have originated from bats. To investigate the potential for future outbreaks, we generated a Japanese bat-derived MERS-related coronavirus, designated EjCoV-3, using reverse genetics. Our results showed that EjCoV-3 does not utilize ACE2 and DPP4, cell entry receptors for SARS-CoV and MERS-CoV, as a means of infection. However, we found that EjCoV-3 is the first bat merbecovirus capable of efficiently replicating in human respiratory cells and the respiratory tract of hamsters. These findings provide new insight into the potential for MERS-related coronaviruses that do not use ACE2 and DPP4 to infect the human respiratory tract, highlighting the importance of preparedness for outbreaks caused by these viruses.</p>","PeriodicalId":17583,"journal":{"name":"Journal of Virology","volume":" ","pages":"e0072725"},"PeriodicalIF":3.8000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282129/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>In vitro</i> and <i>in vivo</i> characterization of a bat merbecovirus with ACE2- and DPP4-independent cell entry.\",\"authors\":\"Hiromichi Matsugo, Tomoya Kitamura, Naohiro Takahashi, James Chambers, Ayano Ichikawa, Misa Katayama, Kaixin Li, Wataru Sekine, Kosuke Ohira, Hiroho Ishida, Akiko Takenaka-Uema, Kazuyuki Uchida, Masayuki Shimojima, Taisuke Horimoto, Shin Murakami\",\"doi\":\"10.1128/jvi.00727-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Betacoronaviruses, which have caused three human outbreaks within the last two decades, are thought to originate from bats, raising the concern that bat coronaviruses could cause a novel human outbreak in the future. To determine whether the bat merbecovirus EjCoV-3 strain, previously detected in <i>Eptesicus japonensis</i> in Japan, has the potential to infect humans, we analyzed its cellular entry mechanism. Cellular entry of EjCoV-3 via the spike protein requires protease treatment and is mediated by an unknown receptor, other than DPP4 or ACE2. We generated cultivable recombinant EjCoV-3 using bacterial artificial chromosome-based reverse genetics and found that it efficiently replicated in human respiratory and intestinal cell cultures as well as nasal ciliated epithelium in hamsters. These findings suggest that bat merbecovirus with ACE2- and DPP4-independent cell entry has the potential to cause human infections, highlighting the importance of extensive bat surveillance for pandemic preparedness.</p><p><strong>Importance: </strong>Betacoronaviruses, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and SARS-CoV-2, have caused three significant outbreaks in the past two decades and are believed to have originated from bats. To investigate the potential for future outbreaks, we generated a Japanese bat-derived MERS-related coronavirus, designated EjCoV-3, using reverse genetics. Our results showed that EjCoV-3 does not utilize ACE2 and DPP4, cell entry receptors for SARS-CoV and MERS-CoV, as a means of infection. However, we found that EjCoV-3 is the first bat merbecovirus capable of efficiently replicating in human respiratory cells and the respiratory tract of hamsters. These findings provide new insight into the potential for MERS-related coronaviruses that do not use ACE2 and DPP4 to infect the human respiratory tract, highlighting the importance of preparedness for outbreaks caused by these viruses.</p>\",\"PeriodicalId\":17583,\"journal\":{\"name\":\"Journal of Virology\",\"volume\":\" \",\"pages\":\"e0072725\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12282129/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1128/jvi.00727-25\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Virology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/jvi.00727-25","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在过去20年里,冠状病毒曾三次引发人类疫情,人们认为它起源于蝙蝠,这引发了人们对蝙蝠冠状病毒可能在未来引发新的人类疫情的担忧。为了确定先前在日本野按蚊中检测到的蝙蝠merbecvirus EjCoV-3株是否具有感染人类的潜力,我们分析了其细胞进入机制。EjCoV-3通过刺突蛋白进入细胞需要蛋白酶处理,并由一种未知受体介导,而不是DPP4或ACE2。我们利用细菌人工染色体反向遗传学技术获得了可培养的重组EjCoV-3,并发现其在人呼吸道和肠道细胞培养物以及仓鼠鼻纤毛上皮中可有效复制。这些发现表明,不依赖ACE2-和dpp4进入细胞的蝙蝠merbecv有可能引起人类感染,这突出了广泛监测蝙蝠对大流行防备的重要性。重要性:乙型冠状病毒,包括严重急性呼吸综合征冠状病毒(SARS-CoV)、中东呼吸综合征冠状病毒(MERS-CoV)和SARS-CoV-2,在过去二十年中引起了三次重大疫情,据信起源于蝙蝠。为了调查未来爆发的可能性,我们使用反向遗传学方法生成了一种日本蝙蝠衍生的mers相关冠状病毒,命名为EjCoV-3。我们的结果表明,EjCoV-3不利用SARS-CoV和MERS-CoV的细胞进入受体ACE2和DPP4作为感染手段。然而,我们发现EjCoV-3是第一个能够在人类呼吸细胞和仓鼠呼吸道中有效复制的蝙蝠merbecv病毒。这些发现为不使用ACE2和DPP4的mers相关冠状病毒感染人类呼吸道的可能性提供了新的见解,突出了对这些病毒引起的疫情做好准备的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and in vivo characterization of a bat merbecovirus with ACE2- and DPP4-independent cell entry.

Betacoronaviruses, which have caused three human outbreaks within the last two decades, are thought to originate from bats, raising the concern that bat coronaviruses could cause a novel human outbreak in the future. To determine whether the bat merbecovirus EjCoV-3 strain, previously detected in Eptesicus japonensis in Japan, has the potential to infect humans, we analyzed its cellular entry mechanism. Cellular entry of EjCoV-3 via the spike protein requires protease treatment and is mediated by an unknown receptor, other than DPP4 or ACE2. We generated cultivable recombinant EjCoV-3 using bacterial artificial chromosome-based reverse genetics and found that it efficiently replicated in human respiratory and intestinal cell cultures as well as nasal ciliated epithelium in hamsters. These findings suggest that bat merbecovirus with ACE2- and DPP4-independent cell entry has the potential to cause human infections, highlighting the importance of extensive bat surveillance for pandemic preparedness.

Importance: Betacoronaviruses, including severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and SARS-CoV-2, have caused three significant outbreaks in the past two decades and are believed to have originated from bats. To investigate the potential for future outbreaks, we generated a Japanese bat-derived MERS-related coronavirus, designated EjCoV-3, using reverse genetics. Our results showed that EjCoV-3 does not utilize ACE2 and DPP4, cell entry receptors for SARS-CoV and MERS-CoV, as a means of infection. However, we found that EjCoV-3 is the first bat merbecovirus capable of efficiently replicating in human respiratory cells and the respiratory tract of hamsters. These findings provide new insight into the potential for MERS-related coronaviruses that do not use ACE2 and DPP4 to infect the human respiratory tract, highlighting the importance of preparedness for outbreaks caused by these viruses.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信