Evidence map›Paper›PMID 32002752›Full record

ArticleJournal of molecular neuroscience : MN2020

Reduction of Human DNA Contamination in Clinical Cerebrospinal Fluid Specimens Improves the Sensitivity of Metagenomic Next-Generation Sequencing.

Xin-Chao Ji, Lin-Fu Zhou, Chao-Yang Li, Ya-Jun Shi, Meng-Li Wu, Yun Zhang, Xiao-Fei Fei, Gang Zhao

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04864873 (An External Evaluation of a Metagenomic Next Generation Sequencing Workflow for Infection Diagnosis Using Oxford Nanopore Sequencing.), which is not on this map. Cited by 40 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04864873 naunknown statusnot on this mapstarted 2021, after this paper: background citation

An External Evaluation of a Metagenomic Next Generation Sequencing Workflow for Infection Diagnosis Using Oxford Nanopore Sequencing.

TypeinterventionalSponsorCapital and Coast District Health boardRan2021 to 2022Enrolled400ConditionsBacterial InfectionsArmsMetagenomic next generation sequencing using Oxford Nanopore, Standard microbiological diagnostic pathway
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 3 syntheses or guidelines pooled it, 54 citations in OpenAlex.

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  7. Clinical features ofFrontiers in cellular and infection microbiology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xin-Chao JiDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Lin-Fu ZhouDepartment of Neurology, The 987 Hospital of PLA, Baoji, China.
Chao-Yang LiDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Ya-Jun ShiDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Meng-Li WuDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Yun ZhangDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Xiao-Fei FeiDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China.
Gang ZhaoDepartment of Neurology, Xijing Hospital, Air Force Military Medical University, Xi'an, China. gangzhao01@163.com.ORCID http://orcid.org/0000-0002-7679-8683
Xijing Hospital · CN

Funding

National Key Research and Development Plan Precision Medicine Project 2016 YFC0904501
6 · The paper itself

Abstract

Metagenomics next-generation sequencing (mNGS) is increasingly available for the detection of obscure infectious diseases of the central nervous system. However, human DNA contamination from elevated white cells, one of the characteristic cerebrospinal fluid (CSF) features in meningitis patients, greatly reduces the sensitivity of mNGS in the pathogen detection. Currently, effective approaches to selectively reduce host DNA contamination from clinical CSF samples are still lacking. In this study, a total of 20 meningitis patients were enrolled, including 10 definitively diagnosed tuberculous meningitis (TBM) and 10 definite cryptococcal meningitis (CM) cases. To evaluate the effect of reduced human DNA in the sensitivity of mNGS detection, three specimen-processing protocols were performed: (i) To remove human DNA, saponin, a nonionic surfactant, was used to selectively lyse white cells in CSF followed by DNase treatment prior to the extraction of DNA; (ii) to reduce host DNA, CSF was centrifuged to remove human cells, and the supernatant was collected for DNA extraction; and (iii) DNA extraction from the unprocessed specimens was set as the control. We found that saponin processing significantly elevated the NGS unique reads for Cryptococcus (P < 0.01) compared with the control but had no effects for Mycobacterium tuberculosis (P > 0.05). However, detection of centrifuged supernatants improved the NGS unique reads for both TBM and CM compared with controls (P < 0.01). Our results demonstrate that the use of mNGS of centrifuged supernatants from clinical CSF samples in patients with TBM and CM is a simple and effective method to improve the sensitivity of pathogen detection.

Indexed as

AdultAgedCerebrospinal FluidCryptococcusFemaleGenome, BacterialGenome, HumanHigh-Throughput Nucleotide SequencingHumansMaleMeningitis, CryptococcalMetagenomicsMiddle AgedMolecular Diagnostic TechniquesMycobacterium tuberculosisSensitivity and SpecificityCryptococcal meningitisHost DNA contaminationMetagenomic next-generation sequencingSaponinTuberculous meningitis

Identifiers

PMID32002752
OpenAlexW3003455884

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.