Detection of HBV DNA by PCR on HBsAg negative blood donors
- VernacularTitle:HBV DNA PCR检测在HBsAg阴性献血人群中的应用
- Author:
Xiaohua CHEN
;
Bi LIN
;
Baolin LIU
;
Lingguang KONG
- Publication Type:Journal Article
- Keywords:
Hepatitis B virus;
DNA,viral;
Hepatitis B surface antigens;
Blood donors;
Polymerase chain reaction;
Enzyme-linked immunosorbent assay
- From:
Chinese Journal of Laboratory Medicine
2008;31(6):672-674
- CountryChina
- Language:Chinese
-
Abstract:
Objective To define the application value of HBV DNA detection on HBsAg-negative blood donors and assess the necessity for nucleic acid detection.Methods Real-time PCR was used to detect HBV DNA on HBsAg negative blood donors.Pools of eight donor samples were used for NAT testing.Viruses were concentrated by centrifugation and the viral DNA extraction was performed using magnetic beads.If HBV DNA wag positive,serological indicators including HBsAg,anti-HBs,HBeAg, anti-Hbe,total anti-HBc was further detected.Results The HBV DNA detection limit was 25 U/ml.There were four HBV DNA positive cases among 23 225 specimens.and the detection rate was 0.17‰ The further serological examination showed anti-Hbe(+),anti-HBc(+) in the two cases and anti-HBc(+) in one case and anti-Hbs(+),anti-HBc(+)in 1 case.The viral load can range form 50 to 200 U/ml. Conclusions The results indicate that there is false negative possibility in blood screening by ELISA.It is necessary to employ anti-Hbe screening or NAT to blood donors screening.
