| Literature DB >> 29941366 |
Yan Wang1, Jeffrey S Glenn2, Mark A Winters2, Li-Ping Shen3, Ingrid Choong4, Ya-Lun Shi5, Sheng-Li Bi3, Li-Ying Ma6, Hui Zeng7, Fu-Jie Zhang8.
Abstract
In this study, a real-time reverse transcription-polymerase chain reaction (real time RT-PCR) assay targeting 2 genetic segments was established to detect HDV RNA. Utilizing the World Health Organization International Standard for Hepatitis D Virus RNA, the lower limit of detection was 575 IU/mL, and the linearity of quantification ranged from 575,000 IU/mL to 575 IU/mL. 384 HBsAg-positive samples collected from China were tested by this method and HDV antibody detection. Eleven samples were positive for anti-HDV IgG which may persist after HDV resolution, 6 samples were HDV RNA positive, and 5 samples were positive for anti-HDV IgM. This assay showed more sensitivity than the detection of anti-HDV IgM. These data demonstrate that the real-time RT-PCR assay for HDV RNA could be implemented in the clinical detection of HDV infection in chronic HBV-infected patients in China.Entities:
Keywords: Detection; HDV; RNA; Real-time PCR
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Year: 2018 PMID: 29941366 DOI: 10.1016/j.diagmicrobio.2018.05.016
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803