- Case report
- Open Access
Nanopore sequencing of cerebrospinal fluid of three patients with cryptococcal meningitis
European Journal of Medical Research volume 27, Article number: 1 (2022)
Cryptococcal meningitis (CM) has a high morbidity and mortality due to the low detection of Cryptococcus in cerebrospinal fluid (CSF) during the early stage of the disease with traditional methods.
In addition to the traditional methods of India ink staining and cryptococcal antigen (CrAg), we used nanopore sequencing and next-generation sequencing (NGS) to detect pathogenic DNA in CSF samples of three patients with CM. The CSF samples of all three patients were positive by India ink staining and CrAg. NGS also detected Cryptococcus in all three CSF samples. Nanopore sequencing detected Cryptococcus in two CSF samples.
Nanopore sequencing may be useful in assisting with the clinical diagnosis of CM. Further research is needed to determine the sensitivity and specificity of nanopore sequencing of CSF.
Cryptococcal meningitis (CM) is an opportunistic infectious disease of the central nervous system (CNS) with high morbidity and mortality . CM shows nonspecific symptoms, such as headache, fever, vomiting, seizures, and focal neurological deficits [2, 3]. With an increase in the number of immunocompromised patients with Human Immunodeficiency Virus (HIV), cirrhosis and malignancies, CM has become a public health hazard [1,2,3,4,5]. However, CM culture is either time-consuming or lacks sensitivity, while the detection of cryptococcal antigen (CrAg) can produce false negative results [3, 4]. Therefore, a fast and highly efficient method of diagnosis is needed.
Molecular biological methods can detect and identify pathogens rapidly and accurately without requiring culture. Polymerase chain reaction (PCR) is used in the clinical diagnosis of microbes but is limited by DNA fragment quantity. Therefore, metagenomic sequencing was used. The pathogen-positive rate of next-generation sequencing (NGS) was 28.34% in the CSF of patients with CNS infections [5,6,7,8]. In addition, Cryptococcus has a large genome. As a result, NGS has poor specificity in the detection of Cryptococcus, since it can only produce short reads with satisfactory sensitivity. In contrast, nanopore sequencing has the ability to generate long reads and real-time sequencing. Therefore, nanopore sequencing has better specificity than NGS [10, 11, 13,14,15,16,17]. However, the clinical application of nanopore sequencing is currently limited and further study is needed.
This study was conducted in the People’s Hospital of Zhengzhou University. The CSF samples were collected from three patients who provided signed informed consent and stored at − 80 °C from three patients who provided signed informed consent. The samples were only used for this study.
DNA was extracted from the samples with the TIANamp micro DNA kit (DP316, TIANGEN BIOTECH) and sonicated to a size of 150 bp. The DNA libraries were constructed through end repair, adapter ligation, PCR amplification, and sequencing on the BGISEQ-50/MGISEQ-2000 platform. High-quality sequencing data were generated by removing short (< 35 bp), low-quality and human sequence data. The remaining data were aligned to four microbial genome databases.
DNA was extracted by a QIAamp DNA mini kit (QIAGEN 51,304, Valencia, CA, USA). The DNA libraries were constructed using a rapid PCR barcoding kit (SQK-RPB004) and sequenced on Flow Cell R9.4 or R9.5 of a MinION platform. The sequencing data were base-called in fast5 files and demultiplexed in fastq files. After removing the short and low-quality reads, the reads were aligned with the microorganism genome database. Species with identified reads higher than two for ONT data were reported.
The study included one male and two female patients, whose ages were 27, 32 and 60 years, respectively. One patient was exposed to pigeons before the onset of symptoms. All patients presented with headache, fever and stiff neck after infection. One patient experienced a seizure, while another patient had decreased level of consciousness. Medical imaging showed invasion of the meninges. CSF tests revealed elevated intracranial pressure (345–400 mmHg) and increased white blood cell (WBC) counts (1–343 × 106/L). All three patients were positive by CSF India ink staining and CSF CrAg detection but negative by CSF culture (Tables 1 and 2). Magnetic resonance imaging (MRI) showed increased meningeal enhancement in all three cases (Fig. 1).
Nanopore sequencing detected Cryptococcus in two CSF samples (I and II) and NGS detected Cryptococcus in all three CSF samples. Nanopore sequencing produced 17,566 reads and 14,366 reads that were aligned to C. neoformans. NGS yielded 1, 17,394 and 97,979 reads that were aligned to C. neoformans.
All three patients were treated with amphotericin B, flucytosine and fluconazole for 31–46 days, and the symptoms gradually improved. Thereafter, the patients were discharged and continued 12 weeks of outpatient follow-up. The symptoms of headache and fever gradually disappeared, and the haemogram returned to normal.
Conclusions and discussion
CM is caused by inhalation of Cryptococcus from soil, pigeon droppings and rotting vegetation [1,2,3]. CSF culture is the gold standard in the diagnosis of CM but is time-consuming and has a low positive rate. The India ink staining results are variable and dependent on the technician [2, 4]. The detection of CrAg always shows false negative results due to the frontal zone phenomenon [2,3,4]. Genetic testing has been increasingly used as a fast and highly efficient method to diagnose CM. Nanopore sequencing, a molecular biology method, is fast and can generate pathogen sequence information, such as drug resistance, to guide management [10, 11, 13,14,15,16,17].
In this study, three patients were clinically confirmed to have CM by positive detection using CSF culture and India ink staining. Nanopore sequencing detected Cryptococcus in two CSF samples and NGS detected Cryptococcus in all three CSF samples. Nanopore sequencing produced 17,566 reads and 14,366 reads that were aligned to C. neoformans, while NGS yielded 1,17,394 and 97,979 reads that were aligned to C. neoformans. The reads produced by nanopore sequencing were much longer than those produced by NGS. Thus, nanopore sequencing can sequence repetitive regions and structural variants, and provide comprehensive genomic information, such as the phenotype of antimicrobial resistance-encoding genes to help clinicians optimize the selection of antifungal agents for treatment (11, 12, 14, 18, 19).
This study was limited by the small sample size, and it is uncertain whether nanopore sequencing can increase the positive rate of pathogen detection. Therefore, further studies are needed.
Nanopore sequencing with improvements in accuracy could change the diagnosis of infection in the future.
Availability of data and materials
The data sets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Central nervous system
Human Immunodeficiency Virus
Polymerase chain reaction
White blood cell
Magnetic resonance imaging
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This work was supported by the People’s Hospital of Zhengzhou University.
Ethics approval and consent to participate
(a) The patient’s written consent was obtained. (b) The design of the work has been approved by the ethical committees of the Henan Provincial People’s Hospital.
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Jin, K., Wang, X., Qin, L. et al. Nanopore sequencing of cerebrospinal fluid of three patients with cryptococcal meningitis. Eur J Med Res 27, 1 (2022). https://doi.org/10.1186/s40001-021-00625-4
- Nanopore sequencing
- Next-generation sequencing
- Cerebrospinal fluid
- Cryptococcal meningitis