Review Article
The Applications of Nanopore Sequencing Technology in Pathogenic Microorganism Detection
Table 2
Nanopore sequencing can quickly identify pathogens in various clinical samples.
| Sample type | Nucleic acid type | Diagnosis | Sequencing methods | Turnaround time | Pathogen |
| Blackbird brain tissues | DNA | — | — | — | Usutu virus [21] | Whole blood | RNA | — | — | <24 h | Ebola virus [20] | Plasma | RNA | — | Metagenomic sequencing | <6 h | Chikungunya virus [29] | Whole blood | RNA | — | Metagenomic sequencing | <6 h | Ebola virus [29] | Serum | RNA | — | Metagenomic sequencing | <6 h | Hepatitis C virus [29] | Cerebrospinal fluid | DNA | Bacterial meningitis | 16S sequencing | 3 h | L. monocytogenes: S. pneumoniae, P. aeruginosa: K. pneumoniae, etc. [34] | Sputum | DNA | Community-acquired pneumonia | 16S sequencing | 5 h | Haemophilus influenzae pneumonia [30] | Faeces | DNA | Necrotizing enterocolitis | Shotgun metagenomic sequencing | <5 h | Klebsiella pneumoniae and Enterobacter cloacae [28] | Sonication fluid | DNA | Prosthetic joint infections | Metagenomic sequencing | — | Staphylococcus aureus, Cutibacterium acnes, Staphylococcus epidermidis, etc. [35] |
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—, not given.
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