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下一代测序揭示了加纳脑炎的病毒病因:一项前瞻性横断面研究。

Next-generation sequencing reveals viral aetiologies of encephalitis in Ghana: a prospective cross-sectional study.

作者信息

Yeboah Richmond, Gorman Richmond, El-Duah Philip, Osei-Mensa James, Acheampong Henry Kyeremateng, Nyarko-Afriyie Emmanuella, Owusu Michael, Amoako Yaw Ampem, Obiri-Danso Kwasi, Phillips Richard Odame, Corman Victor Max, Drosten Christian, Sylverken Augustina Angelina

机构信息

Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana.

Kwame Nkrumah University of Science and Technology (KNUST), Kumasi, Ghana.

出版信息

BMC Infect Dis. 2025 Aug 8;25(1):1005. doi: 10.1186/s12879-025-11436-x.

Abstract

In Ghana, cerebrospinal fluid polymerase chain reaction (PCR) is the primary diagnostic tool for viral encephalitis. However, its application remains limited, and diagnosis is predominantly syndromic. Current data on encephalitis in Ghana are sparse and often restricted to sporadic cases, with improved PCR diagnostics elucidating some aetiological agents but leaving approximately 60% of cases undiagnosed. This diagnostic gap arises because PCR targets specific pathogens, overlooking unexpected or novel agents. Consequently, tailored patient management is hindered, patient outcomes are adversely affected, and efforts to understand the true burden of viral encephalitis are impeded. To address these challenges, we conducted a cross-sectional study at the Komfo Anokye Teaching Hospital, a major tertiary referral centre in Ghana, from May 2019 to August 2022. Forty-three (43) cerebrospinal fluid samples from suspected encephalitis patients were analysed using Polymerase chain reaction (PCR) and high-throughput next-generation sequencing (NGS) to identify a broader range of viral pathogens and assess the role of co-infections in disease outcomes. Viral encephalitis was detected in 42% (18/43) of samples, revealing 11 viruses across six families. Herpesviruses (34%) and retroviruses (28%) were the most prevalent, with human immunodeficiency virus-1 (HIV-1) and enteroviruses identified as the primary causative agents. NGS identified a broader viral spectrum, detecting 6 additional viruses (HIV-1, EBV, Mumps, HHV-6, HRV, Rotavirus A) which were not targeted by PCR. While NGS and PCR demonstrated comparable sensitivity for certain pathogens, NGS identified additional co-infections (39%, 7/18) and rare viruses. The survival rate for patients with co-infections was 28.6% (2/7), with HIV-1 and herpesviruses implicated in 85.7% (6/7) of co-infected cases. This study highlights the potential of NGS to expand the diagnostic capabilities for viral encephalitis. By overcoming the limitations of PCR, NGS provides a more comprehensive approach, enhancing our understanding of the true burden of viral encephalitis in Ghana and informing better patient management strategies.

摘要

在加纳,脑脊液聚合酶链反应(PCR)是病毒性脑炎的主要诊断工具。然而,其应用仍然有限,诊断主要是基于症状。加纳目前关于脑炎的数据稀少,且往往局限于散发病例,改进后的PCR诊断法阐明了一些病原体,但仍有大约60%的病例未得到诊断。出现这种诊断差距是因为PCR针对特定病原体,忽略了意想不到的或新型病原体。因此,量身定制的患者管理受到阻碍,患者预后受到不利影响,了解病毒性脑炎真实负担的努力也受到阻碍。为应对这些挑战,我们于2019年5月至2022年8月在加纳的主要三级转诊中心孔福·阿诺凯教学医院开展了一项横断面研究。对43份疑似脑炎患者的脑脊液样本进行了聚合酶链反应(PCR)和高通量下一代测序(NGS)分析,以识别更广泛的病毒病原体,并评估合并感染在疾病转归中的作用。42%(18/43)的样本检测出病毒性脑炎,共发现六个病毒科的11种病毒。疱疹病毒(34%)和逆转录病毒(28%)最为常见,人类免疫缺陷病毒1型(HIV-1)和肠道病毒被确定为主要病原体。NGS识别出更广泛的病毒谱,检测到另外6种PCR未靶向的病毒(HIV-1、EB病毒、腮腺炎病毒、HHV-6、鼻病毒、轮状病毒A)。虽然NGS和PCR对某些病原体的敏感性相当,但NGS识别出了更多的合并感染(39%,7/18)和罕见病毒。合并感染患者的生存率为28.6%(2/7),HIV-1和疱疹病毒在85.7%(6/7)的合并感染病例中起作用。这项研究凸显了NGS在扩大病毒性脑炎诊断能力方面的潜力。通过克服PCR的局限性,NGS提供了一种更全面的方法,增强了我们对加纳病毒性脑炎真实负担的理解,并为更好的患者管理策略提供依据。

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本文引用的文献

1
Clinical epidemiology, determinants, and outcomes of viral encephalitis in Ghana; a cross-sectional study.
PLoS One. 2024 Feb 12;19(2):e0297277. doi: 10.1371/journal.pone.0297277. eCollection 2024.
2
Prevention, treatment and cure of HIV infection.
Nat Rev Microbiol. 2023 Oct;21(10):657-670. doi: 10.1038/s41579-023-00914-1. Epub 2023 Jun 21.
3
Etiological Analysis of Viral Encephalitis in Children in Zhejiang Province from 2018 to 2019.
Diagnostics (Basel). 2022 Aug 14;12(8):1964. doi: 10.3390/diagnostics12081964.
5
Rabies is still a fatal but neglected disease: a case report.
J Med Case Rep. 2021 Dec 1;15(1):575. doi: 10.1186/s13256-021-03164-y.
7
Challenges in the application of NGS in the clinical laboratory.
Hum Immunol. 2021 Nov;82(11):812-819. doi: 10.1016/j.humimm.2021.03.011. Epub 2021 Apr 21.
8
Treatment of Viral Encephalitis.
Neurol Clin. 2021 Feb;39(1):197-207. doi: 10.1016/j.ncl.2020.09.011. Epub 2020 Nov 7.
9
Toward Clinical Implementation of Next-Generation Sequencing-Based Genetic Testing in Rare Diseases: Where Are We?
Trends Genet. 2019 Nov;35(11):852-867. doi: 10.1016/j.tig.2019.08.006. Epub 2019 Oct 14.
10
Next-generation sequencing and its clinical application.
Cancer Biol Med. 2019 Feb;16(1):4-10. doi: 10.20892/j.issn.2095-3941.2018.0055.

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