Novel hepatitis B virus surface antigen mutations associated with occult genotype B hepatitis B virus infection affect HBsAg detection. Issue 9 (11th May 2020)

• Record Type: Journal Article
• Authors: Wang, Hao; Wang, Min; Huang, Jieting; Xu, Ru; Liao, Qiao; Shan, Zhengang; Zheng, Yourong; Rong, Xia; Tang, Xi; Li, Tingting; Wang, Wenjing; Li, Chengyao; Fu, Yongshui
• Is Part Of: Journal of viral hepatitis. Volume 27:Issue 9(2020)
• Page Start: 915
• Page End: 921
• Publication Date: 2020-05-11
• Subjects: hepatitis B surface antigen -- hepatitis B virus -- mutation -- occult hepatitis B infection; Hepatitis, Viral -- Periodicals; Hepatitis, Viral, Animal; Hepatitis, Viral, Human; 616.3623
• DOI: 10.1111/jvh.13309
• Languages: English
• ISSNs: 1352-0504

Abstract

Abstract: The causative factors of occult hepatitis B infection are complicated and not yet been fully elucidated. Mutations in hepatitis B virus (HBV) S gene are one of the factors may contributing to occult infection. In this study, 89 blood donors with genotype B occult HBV infection were investigated. Fifty‐seven hepatitis B surface antigen (HBsAg)‐positive/HBV DNA‐positive blood donors served as control group for comparison. Occult HBV‐related mutations with a high incidence ( P < .05) in the S gene were identified. To further verify these occult infection‐related mutations, a conservative full‐gene expression vector of HBV B genotype (pHBV1.3B) was constructed. Then, the mutant plasmids on the basis of pHBV1.3B were constructed and transfected into HepG2 cells. Extracellular as well as intracellular HBsAg was analysed by electrochemical luminescence and cellular immunohistochemistry. Ten occult infection‐related mutations (E2G, Q101R, K122R, M133T, D144E, G145R, V168A, S174N, L175S and I226S) were significantly more frequent in the occult infection group ( P < .05). Five of the ten mutations (E2G, D144E, G145R, V168A and S174N) strongly decreased extracellular HBsAg level ( P < .05) in the transfection system. Notably, the E2G mutation had the most significant impact on the ratio of extracellular HBsAg (3.8% vs pHBV1.3B) and intracellular HBsAg (239.3% vs pHBV1.3B) ( P < .05), and the fluorescence density of E2G mutant HBsAg was significantly higher than that of pHBV1.3B ( P < .0001). Hence, ten mutations were associated with genotype B occult HBV infection; E2G and V168A were novel mutations which we confirmed significantly affect HBsAg detection. E2G might cause HBsAg secretion impairment that results in intracellular accumulation and a decrease in HBsAg secretion.