Department of Infectious Disease, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.
State Key Laboratory of Neurology and Oncology Drug Development, Jiangsu Simcere Pharmaceutical Co.,Ltd, Jiangsu Simcere Diagnostics Co.,Ltd., Nanjing, China.
Ann Clin Microbiol Antimicrob. 2024 Feb 29;23(1):22. doi: 10.1186/s12941-024-00682-7.
Early and accurate etiological diagnosis is very important for improving the prognosis of central nervous system (CNS) infections in human immunodeficiency virus (HIV)-infected patients. The goal is not easily achieved by conventional microbiological tests. We developed a nanopore targeted sequencing (NTS) platform and evaluated the diagnostic performance for CNS infections in HIV-infected patients, with special focus on cryptococcal meningitis (CM). We compared the CM diagnostic performance of NTS with conventional methods and cryptococcal polymerase chain reaction (PCR).
This study included 57 hospitalized HIV-infected patients with suspected CNS infections from September 2018 to March 2022. The diagnosis established during hospitalization includes 27 cases of CM, 13 CNS tuberculosis, 5 toxoplasma encephalitis, 2 cytomegalovirus (CMV) encephalitis and 1 Varicella-zoster virus (VZV) encephalitis. The 2 cases of CMV encephalitis also have co-existing CM. Target-specific PCR amplification was used to enrich pathogen sequences before nanopore sequencing. NTS was performed on stored cerebrospinal fluid (CSF) samples and the results were compared with the diagnosis during hospitalization.
53 (93.0%) of the patients were male. The median CD4 cell count was 25.0 (IQR: 14.0-63.0) cells/uL. The sensitivities of CSF culture, India ink staining, cryptococcal PCR and NTS for CM were 70.4% (95%CI: 51.5 - 84.1%), 76.0% (95%CI: 56.6 - 88.5%), 77.8% (59.2 - 89.4%) and 85.2% (95%CI: 67.5 - 94.1%), respectively. All those methods had 100% specificity for CM. Our NTS platform could identify Cryptococcus at species level. Moreover, NTS was also able to identify all the 5 cases of toxoplasma encephalitis, 2 cases of CMV encephalitis and 1 VZV encephalitis. However, only 1 of 13 CNS tuberculosis cases was diagnosed by NTS, and so did Xpert MTB/RIF assay.
NTS has a good diagnostic performance for CM in HIV-infected patients and may have the ability of simultaneously detecting other pathogens, including mixed infections. With continuing improving of the NTS platform, it may be a promising alterative microbiological test for assisting with the diagnosis of CNS infections.
早期、准确的病因诊断对于改善人类免疫缺陷病毒(HIV)感染患者中枢神经系统(CNS)感染的预后非常重要。常规微生物学检测往往难以实现这一目标。我们开发了一种纳米孔靶向测序(NTS)平台,并评估了其在 HIV 感染患者 CNS 感染中的诊断性能,特别关注隐球菌性脑膜炎(CM)。我们将 NTS 与常规方法和隐球菌聚合酶链反应(PCR)检测 CM 的诊断性能进行了比较。
本研究纳入了 2018 年 9 月至 2022 年 3 月期间因疑似 CNS 感染住院的 57 例 HIV 感染患者。住院期间确诊的疾病包括 27 例 CM、13 例中枢神经系统结核、5 例弓形虫脑炎、2 例巨细胞病毒(CMV)脑炎和 1 例水痘带状疱疹病毒(VZV)脑炎。2 例 CMV 脑炎也合并有 CM。在进行纳米孔测序之前,使用靶向特异性 PCR 扩增来富集病原体序列。对储存的脑脊液(CSF)样本进行 NTS,并将结果与住院期间的诊断进行比较。
53 例(93.0%)患者为男性。中位 CD4 细胞计数为 25.0(IQR:14.0-63.0)个/μL。CSF 培养、印度墨水染色、隐球菌 PCR 和 NTS 对 CM 的敏感度分别为 70.4%(95%CI:51.5-84.1%)、76.0%(95%CI:56.6-88.5%)、77.8%(59.2-89.4%)和 85.2%(95%CI:67.5-94.1%)。所有这些方法对 CM 的特异性均为 100%。我们的 NTS 平台能够鉴定出隐球菌的种属水平。此外,NTS 还能够鉴定出所有 5 例弓形虫脑炎、2 例 CMV 脑炎和 1 例 VZV 脑炎。然而,只有 13 例中枢神经系统结核病例中的 1 例和 Xpert MTB/RIF 检测通过 NTS 确诊。
NTS 对 HIV 感染患者的 CM 具有良好的诊断性能,并且可能具有同时检测其他病原体的能力,包括混合感染。随着 NTS 平台的不断改进,它可能成为一种有前途的替代微生物学检测方法,有助于 CNS 感染的诊断。