Abstract
Hepatitis B virus RNA is detectable in the serum of infected patients; however, the RNA species has been questioned. We tested 1827 specimens using a quantitative dual-target quantitative polymerase chain reaction assay and determined that full-length pregenomic RNA is the primary source. These results clarify the major identity of circulating HBV RNA species.
Original language | English |
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Pages (from-to) | 2029-2031 |
Number of pages | 3 |
Journal | Clinical infectious diseases : an official publication of the Infectious Diseases Society of America |
Volume | 72 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1 Jun 2021 |
Keywords
- hepatitis B virus
- pregenomic RNA
- quantitative polymerase chain reaction
- viral diagnostic assay