Metagenomic next-generation sequencing for etiological diagnosis of an unexpected rabies case with unclear exposure history.

IF 3 3区 医学 Q2 INFECTIOUS DISEASES BMC Infectious Diseases Pub Date : 2025-02-24 DOI:10.1186/s12879-025-10687-y
Jing Wu, Yingjie Qi, Wenyan Zhang, Lixue Liu, Jiangrong Chen, Yun Yang, Xuanshun Zhang, Xinru Liu, Yuru Shi
{"title":"Metagenomic next-generation sequencing for etiological diagnosis of an unexpected rabies case with unclear exposure history.","authors":"Jing Wu, Yingjie Qi, Wenyan Zhang, Lixue Liu, Jiangrong Chen, Yun Yang, Xuanshun Zhang, Xinru Liu, Yuru Shi","doi":"10.1186/s12879-025-10687-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Rabies is an acute and lethal zoonotic disease caused by the rabies virus (RABV). After onset, there are no effective drugs or treatment methods.</p><p><strong>Case presentation: </strong>A 49-year-old female from Hefei, Anhui Province, China, presented to a local hospital with fever, pruritus, chest distress, and shortness of breath. During the consultation, the patient exhibited agitation and was later admitted to the intensive care unit (ICU) in the local hospital for endotracheal intubation and mechanical ventilation due to worsened agitation and dyspnea. Cerebrospinal fluid (CSF) and blood samples were collected and pathogenic microorganism identification was performed by culture and mNGS. However, all results were negative. In addition, the patient did not display typical rabies-specific symptoms such as aerophobia, hydrophobia or photophobia from onset to admission. Subsequently, saliva samples were collected for mNGS detection following consultation with experts at our hospital. Nucleic acid sequences uniquely aligned to the rabies virus (RABV) were identified in these samples. The result was further confirmed by local Center for Disease Control and Prevention (CDC) through RT-qPCR which detected part of the N gene of RABV in the saliva sample. The patient was then transferred to the ICU for isolation. Unfortunately, the patient died on the 10th day of admission due to multiple organ failure. The detection of human rabies virus IgG antibodies reported positive during the advanced stage of the disease during the hospitalization. We consistently verified with the patient's family member that there was no clear history of animal bites and no history of RABV vaccination. Furthermore, we performed phylogenetic analysis of partial L and G gene sequences of RABV obtained by mNGS (designated HFG23-L and HFG23-G, respectively), the results showed that both HFG23-L and HFG23-G belonged to the China I lineage, and shared 99.7% similarity with the Fengtai strain isolated from dogs in Beijing.</p><p><strong>Conclusions: </strong>The identification of unique RABV sequence through mNGS in the patient's saliva sample suggested that mNGS could serve as a valuable screening tool for the etiological diagnosis of rabies, especially when timely laboratory testing was unavailable or when patients lacked non-specific prodromal symptom and clear exposure history.</p>","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":"25 1","pages":"258"},"PeriodicalIF":3.0000,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11849319/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12879-025-10687-y","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Rabies is an acute and lethal zoonotic disease caused by the rabies virus (RABV). After onset, there are no effective drugs or treatment methods.

Case presentation: A 49-year-old female from Hefei, Anhui Province, China, presented to a local hospital with fever, pruritus, chest distress, and shortness of breath. During the consultation, the patient exhibited agitation and was later admitted to the intensive care unit (ICU) in the local hospital for endotracheal intubation and mechanical ventilation due to worsened agitation and dyspnea. Cerebrospinal fluid (CSF) and blood samples were collected and pathogenic microorganism identification was performed by culture and mNGS. However, all results were negative. In addition, the patient did not display typical rabies-specific symptoms such as aerophobia, hydrophobia or photophobia from onset to admission. Subsequently, saliva samples were collected for mNGS detection following consultation with experts at our hospital. Nucleic acid sequences uniquely aligned to the rabies virus (RABV) were identified in these samples. The result was further confirmed by local Center for Disease Control and Prevention (CDC) through RT-qPCR which detected part of the N gene of RABV in the saliva sample. The patient was then transferred to the ICU for isolation. Unfortunately, the patient died on the 10th day of admission due to multiple organ failure. The detection of human rabies virus IgG antibodies reported positive during the advanced stage of the disease during the hospitalization. We consistently verified with the patient's family member that there was no clear history of animal bites and no history of RABV vaccination. Furthermore, we performed phylogenetic analysis of partial L and G gene sequences of RABV obtained by mNGS (designated HFG23-L and HFG23-G, respectively), the results showed that both HFG23-L and HFG23-G belonged to the China I lineage, and shared 99.7% similarity with the Fengtai strain isolated from dogs in Beijing.

Conclusions: The identification of unique RABV sequence through mNGS in the patient's saliva sample suggested that mNGS could serve as a valuable screening tool for the etiological diagnosis of rabies, especially when timely laboratory testing was unavailable or when patients lacked non-specific prodromal symptom and clear exposure history.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
元基因组下一代测序用于暴露史不明确的意外狂犬病病例的病原学诊断。
背景:狂犬病是由狂犬病毒(RABV)引起的一种急性致死性人畜共患疾病。发病后,没有有效的药物或治疗方法。病例介绍:一名来自中国安徽省合肥市的49岁女性,因发热、瘙痒、胸闷和呼吸短促到当地医院就诊。在会诊期间,患者表现出躁动,随后因躁动和呼吸困难加重而入住当地医院重症监护病房(ICU)进行气管插管和机械通气。采集脑脊液(CSF)和血液标本,采用培养法和mNGS法进行病原微生物鉴定。然而,所有结果均为阴性。此外,从发病到入院,患者未表现出典型的狂犬病特异性症状,如恐空、恐水或恐光。随后与我院专家会诊,采集唾液样本进行mNGS检测。在这些样本中鉴定出与狂犬病毒(RABV)唯一一致的核酸序列。当地疾病预防控制中心(CDC)通过RT-qPCR检测唾液样本中RABV的部分N基因进一步证实了这一结果。随后将患者转至ICU进行隔离。不幸的是,患者在入院第10天因多器官衰竭死亡。人狂犬病毒IgG抗体检测报告阳性在疾病晚期住院期间。我们与患者的家庭成员一致核实,无明确的动物咬伤史,也无RABV疫苗接种史。对mNGS获得的RABV部分L和G基因序列(分别命名为HFG23-L和HFG23-G)进行系统发育分析,结果表明HFG23-L和HFG23-G均属于中国I系,与北京地区犬分离的丰台株相似度为99.7%。结论:通过mNGS在患者唾液样本中鉴定出独特的RABV序列,提示mNGS可作为一种有价值的狂犬病病原学诊断筛查工具,特别是在无法及时进行实验室检测或患者缺乏非特异性前体症状和明确暴露史的情况下。
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 去求助
来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
期刊最新文献
Cohort evaluation of an all-oral shorter regimen for drug-resistant tuberculosis in Ecuador. A machine learning-based prediction model for treatment efficacy in smear and/or chest X-ray positive tuberculosis patients. Comparative analysis of parenchymal and extraparenchymal neurocysticercosis: a 10-year experience from northern Thailand. Prevalence and determinants of hepatitis B virus infection among youth in southern-central Ethiopia: a community-based cross-sectional study. Seroprevalence of endemic and emergent coronaviruses among SARS-COV-2 patients and healthcare workers in Abidjan, Côte d'Ivoire.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1