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Nanopore sequencing of cerebrospinal fluid of three patients with cryptococcal meningitis

BACKGROUND: 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. CASE PRESENTATION: In addition to the traditional methods of India ink staining and crypto...

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Detalles Bibliográficos
Autores principales: Jin, Ke, Wang, Xiaojuan, Qin, Lingzhi, Jia, Yazhen, Zhou, Keke, Jiang, Yusu, Zhang, Milan, Zhang, Tao, Zhang, Mengge, Ma, Weifeng, Jia, Lin, Teng, Yongshi, Dai, Shuhua, li, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722347/
https://www.ncbi.nlm.nih.gov/pubmed/34980252
http://dx.doi.org/10.1186/s40001-021-00625-4
Descripción
Sumario:BACKGROUND: 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. CASE PRESENTATION: 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. CONCLUSION: 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.