This study provides significant new data on the application of metagenomic next-generation sequencing (mNGS) to clinical diagnostics of central nervous system (CNS) viral infections, which can have high mortality rates and severe sequelae. Conventional diagnostic procedures for identifying viruses can be inefficient and rely on preconceived assumptions about the pathogen, making mNGS an appealing alternative. However, the effectiveness of mNGS is affected by the presence of human DNA contamination, which can be minimized by using cell-free DNA (cfDNA) instead of whole-cell DNA (wcDNA). This multi-center retrospective study of patients with suspected viral CNS infection found that mNGS using cfDNA had a significantly lower proportion of human DNA and higher sensitivity for detecting viruses than mNGS using wcDNA. Herpesviruses, particularly VZV, were found to be the most common DNA viruses in these patients. Overall, mNGS using cfDNA is a promising complementary diagnostic method for detecting CNS viral infections.
Keyphrases
- circulating tumor
- cell free
- single molecule
- endothelial cells
- sars cov
- circulating tumor cells
- end stage renal disease
- blood brain barrier
- chronic kidney disease
- randomized controlled trial
- induced pluripotent stem cells
- ejection fraction
- newly diagnosed
- antibiotic resistance genes
- systematic review
- copy number
- risk assessment
- stem cells
- single cell
- genetic diversity
- drinking water
- risk factors
- coronary artery disease
- machine learning
- mesenchymal stem cells
- bone marrow
- early onset
- microbial community
- heavy metals
- human health