Morsli Madjid, Kerharo Quentin, Delerce Jeremy, Roche Pierre-Hugues, Troude Lucas, Drancourt Michel
IHU Méditerranée Infection, 13005 Marseille, France.
Aix-Marseille-Université, IRD, MEPHI, IHU Méditerranée Infection, 13005 Marseille, France.
Pathogens. 2021 Apr 12;10(4):461. doi: 10.3390/pathogens10040461.
Current routine real-time PCR methods used for the point-of-care diagnosis of infectious meningitis do not allow for one-shot genotyping of the pathogen, as in the case of deadly meningitis. Real-time PCR diagnosed meningitis in a 22-year-old male patient, during his hospitalisation following a more than six-metre fall. Using an Oxford Nanopore Technologies real-time sequencing run in parallel to real-time PCR, we detected the genome directly from the cerebrospinal fluid sample in six hours. Furthermore, BLAST analysis of the sequence encoding for a partial DUF417 domain-containing protein diagnosed a non-b serotype, non-typeable belonging to lineage 22.1-21. The Oxford Nanopore metagenomic next-generation sequencing approach could be considered for the point-of-care diagnosis of infectious meningitis, by direct identification of pathogenic genomes and their genotypes/serotypes.
目前用于感染性脑膜炎即时诊断的常规实时PCR方法,无法像在致命性脑膜炎病例中那样对病原体进行一次性基因分型。一名22岁男性患者在从超过6米高处坠落住院期间,通过实时PCR诊断为脑膜炎。我们使用与实时PCR并行运行的牛津纳米孔技术实时测序,在6小时内直接从脑脊液样本中检测到了基因组。此外,对编码部分含DUF417结构域蛋白的序列进行BLAST分析,诊断出一种属于22.1-21分支的非b血清型、不可分型菌株。通过直接鉴定致病基因组及其基因型/血清型,牛津纳米孔宏基因组下一代测序方法可用于感染性脑膜炎的即时诊断。