Table 1.
Method | Virus Nucleic Acid Detected |
Shortcomings | Advantages | |
---|---|---|---|---|
Metaviromics or viral metagenomics |
RNA or DNA viral genomes in the extracellular stage | RNA viruses targeted separately than DNA viruses Needs special enrichment for dsRNA and ssDNA Large DNA viruses are filtered out High-burst-size viruses can be overrepresented |
Enriched for viral sequences, better assembly | |
Metatranscriptomics | Transcripts of (+) and (−) ssRNA, dsRNA, ssDNA, dsDNA | High background of nonviral sequences Potentially fragmented assemblies Misses low-titre viruses Does not distinguish between (+) ssRNA viral genome and transcripts |
Captures all types of DNA and RNA viruses simultaneously Captures active infection (for DNA viruses) Can capture RNA viruses without capsids |
|
dsRNA sequencing | ssRNA as replicative intermediate dsRNA genomes |
Not as effective for (−) ssRNA and DNA viruses Cellular metatranscriptomes are removed in the enrichment process |
Enriched for RNA viruses Can be used for detection of both extracellular (<0.22 µm fractions) and intracellular RNA viruses |