Five-year longitudinal surveillance reveals the continual circulation of both alpha- and beta-coronaviruses in Plateau and Gansu pikas (Ochotona spp.) at Qinghai Lake, China1.

IF 8.4 2区 医学 Q1 IMMUNOLOGY
Emerging Microbes & Infections Pub Date : 2024-12-01 Epub Date: 2024-08-24 DOI:10.1080/22221751.2024.2392693
Lin Xu, Meiqing Song, Xianzhi Tian, Ju Sun, Yanjun Wang, Mengyu Bie, Yuhai Bi, Edward C Holmes, Yi Guan, Jianjun Chen, Juan Li, Weifeng Shi
{"title":"Five-year longitudinal surveillance reveals the continual circulation of both alpha- and beta-coronaviruses in Plateau and Gansu pikas (<i>Ochotona</i> spp.) at Qinghai Lake, China<sup>1</sup>.","authors":"Lin Xu, Meiqing Song, Xianzhi Tian, Ju Sun, Yanjun Wang, Mengyu Bie, Yuhai Bi, Edward C Holmes, Yi Guan, Jianjun Chen, Juan Li, Weifeng Shi","doi":"10.1080/22221751.2024.2392693","DOIUrl":null,"url":null,"abstract":"<p><p>The discovery of alphacoronaviruses and betacoronaviruses in plateau pikas (<i>Ochotona curzoniae</i>) expanded the host range of mammalian coronavirus (CoV) to a new order - Lagomorpha. However, the diversity and evolutionary relationships of CoVs in these plateau-region-specific animal population remains uncertain. We conducted a five-year longitudinal surveillance of CoVs harboured by pikas around Qinghai Lake, China. CoVs were identified in 33 of 236 plateau pikas and 2 of 6 Gansu pikas (<i>Ochotona cansus</i>), with a total positivity rate of 14.5%, and exhibiting a wide spatiotemporal distribution across seven sampling sites and six time points. Through meta-transcriptomic sequencing and RT-PCR, we recovered 16 near-complete viral genome sequences. Phylogenetic analyses classified the viruses as variants of either pika alphacoronaviruses or betacoronaviruses endemic to plateau pikas from the Qinghai-Tibet Plateau region. Of particular note, the pika-associated betacoronaviruses may represent a novel subgenus within the genus <i>Betacoronavirus</i>. Tissue tropism, evaluated using quantitative real-time PCR, revealed the presence of CoV in the rectal and/or lung tissues, with the highest viral loads at 10<sup>3.55</sup> or 10<sup>2.80</sup> RNA copies/μL. Surface plasmon resonance (SPR) assays indicated that the newly identified betacoronavirus did not bind to human or pika Angiotensin-converting enzyme 2 (ACE2) or Dipeptidyl peptidase 4 (DPP4). The findings highlight the ongoing circulation and broadening host spectrum of CoVs among pikas, emphasizing the necessity for further investigation to evaluate their potential public health risks.</p>","PeriodicalId":11602,"journal":{"name":"Emerging Microbes & Infections","volume":" ","pages":"2392693"},"PeriodicalIF":8.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11346322/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Emerging Microbes & Infections","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/22221751.2024.2392693","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/24 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The discovery of alphacoronaviruses and betacoronaviruses in plateau pikas (Ochotona curzoniae) expanded the host range of mammalian coronavirus (CoV) to a new order - Lagomorpha. However, the diversity and evolutionary relationships of CoVs in these plateau-region-specific animal population remains uncertain. We conducted a five-year longitudinal surveillance of CoVs harboured by pikas around Qinghai Lake, China. CoVs were identified in 33 of 236 plateau pikas and 2 of 6 Gansu pikas (Ochotona cansus), with a total positivity rate of 14.5%, and exhibiting a wide spatiotemporal distribution across seven sampling sites and six time points. Through meta-transcriptomic sequencing and RT-PCR, we recovered 16 near-complete viral genome sequences. Phylogenetic analyses classified the viruses as variants of either pika alphacoronaviruses or betacoronaviruses endemic to plateau pikas from the Qinghai-Tibet Plateau region. Of particular note, the pika-associated betacoronaviruses may represent a novel subgenus within the genus Betacoronavirus. Tissue tropism, evaluated using quantitative real-time PCR, revealed the presence of CoV in the rectal and/or lung tissues, with the highest viral loads at 103.55 or 102.80 RNA copies/μL. Surface plasmon resonance (SPR) assays indicated that the newly identified betacoronavirus did not bind to human or pika Angiotensin-converting enzyme 2 (ACE2) or Dipeptidyl peptidase 4 (DPP4). The findings highlight the ongoing circulation and broadening host spectrum of CoVs among pikas, emphasizing the necessity for further investigation to evaluate their potential public health risks.

为期五年的纵向监测显示,α-和β-冠状病毒在中国青海湖的高原鼠兔和甘肃鼠兔(Ochotona spp.)
摘要 在高原鼠兔(Ochotona curzoniae)中发现的阿尔法冠状病毒(alphacoronaviruses)和贝他冠状病毒(betacoronaviruses)将哺乳动物冠状病毒(CoV)的宿主范围扩大到了一个新的目--Lagomorpha。然而,这些高原地区特有的动物种群中CoV的多样性和进化关系仍不确定。我们对中国青海湖周边鼠兔携带的CoV进行了为期五年的纵向监测。在 236 只高原鼠兔中的 33 只和 6 只甘肃鼠兔(Ochotona cansus)中的 2 只发现了 CoVs,总阳性率为 14.5%,并在 7 个采样点和 6 个时间点上呈现出广泛的时空分布。通过元转录组测序和 RT-PCR,我们恢复了 16 个几乎完整的病毒基因组序列。系统发生学分析将这些病毒归类为青藏高原地区特有的鼠兔α-冠状病毒或β-冠状病毒的变种。特别值得注意的是,与鼠兔相关的betacoronaviruses可能代表了Betacoronavirus属中的一个新亚属。使用定量实时聚合酶链式反应(real-time PCR)对组织趋向性进行评估后发现,CoV存在于直肠和/或肺组织中,最高病毒载量为103.55或102.80 RNA拷贝/μL。表面等离子体共振(SPR)测定表明,新发现的betacoronavirus不与人或鼠兔血管紧张素转换酶2(ACE2)或二肽基肽酶4(DPP4)结合。这些发现突显了CoVs在鼠兔中的持续传播和宿主谱的不断扩大,强调了进一步调查以评估其潜在公共卫生风险的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
×
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:481959085
Book学术官方微信