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The Feasibility of Metagenomic Next-Generation Sequencing to Identify Pathogens Causing Tuberculous Meningitis in Cerebrospinal Fluid

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机构: [1]Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China, [2]Department of Neurology, Beijing Children’s Hospital, Capital Medical University, Beijing, China, [3]Department of Neurology, Zhujiang Hospital, Southern Medical University, Guangzhou, China, [4]Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China, [5]Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China, [6]BGI Genomics, BGI-Shenzhen, Shenzhen, China, [7]Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China
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关键词: cerebrospinal fluid Mycobacterium tuberculosis meningitis metagenomic next-generation sequencing early diagnosis

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Purpose: The application of metagenomic next-generation sequencing (mNGS) in the diagnosis of tuberculous meningitis (TBM) remains poorly characterized. Here, we retrospectively analyzed data from patients with TBM who had taken both mNGS and conventional tests including culture of Mycobacterium tuberculosis (MTB), polymerase chain reaction (PCR) and acid-fast bacillus (AFB) stain, and the sensitivity and specificity of these methods were compared. Methods: We retrospectively recruited TBM patients admitted to the hospital between December 2015 and October 2018. The first collection of cerebrospinal fluid (CSF) samples underwent both mNGS and conventional tests. In addition, patients with bacterial/cryptococcal meningitis or viral meningoencephalitis were mNGS positive controls, and a patient with auto-immune encephalitis was an mNGS negative control. Results: Twenty three TBM patients were classified as 12 definite and 11 clinical diagnoses, which were based on clinical manifestations, pathogen evidence, CSF parameters, brain imaging, and treatment response. The mNGS method identified sequences of Mycobacterium tuberculosis complex (MBTC) from 18 samples (18/23, 78.26%). In patients with definite TBM, the sensitivity of mNGS, AFB, PCR, and culture to detect MTB in the first CSF samples were 66.67, 33.33, 25, and 8.33%, respectively. The specificity of each method was 100%. Among the four negative mNGS cases (4/23, 17.39%), three turned out positive by repeated AFB stain. The agreement of mNGS with the total of conventional methods was 44.44% (8/18). Combination of mNGS and conventional methods increased the detection rate to 95.65%. One patient was diagnosed as complex of TBM and cryptococcal meningitis, in which AFB stain and cryptococcal antigen enzyme immunoassay were positive and the DNA of Ctyptococcus neofolmans was detected by mNGS. Conclusion: Our study indicates that mNGS is an alternative method to detect the presence of mycobacterial DNA in CSF samples from patients with TBM and deserves to be applied as a front-line CSF test.

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出版当年[2018]版:
大类 | 2 区 生物
小类 | 2 区 微生物学
最新[2023]版:
大类 | 2 区 生物学
小类 | 3 区 微生物学
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出版当年[2017]版:
Q2 MICROBIOLOGY
最新[2023]版:
Q2 MICROBIOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2017版] 出版当年五年平均 出版前一年[2016版] 出版后一年[2018版]

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第一作者机构: [1]Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China,
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通讯机构: [1]Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China, [7]Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China
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