Institute of Clinical Blood Transfusion, Guangzhou Blood Center, Guangzhou, Guangdong, China.
The Key Medical Laboratory of Guangzhou, Guangzhou, Guangdong, China.
Sci Rep. 2022 May 17;12(1):8194. doi: 10.1038/s41598-022-12288-0.
The characteristics of a large sample size of the full-length genome of occult hepatitis B virus (HBV) infection (OBI) have not been extensively explored in China. Voluntary blood donors who were HBsAg-negative/HBV NAT-positive (HBsAg-/HBV NAT+) were identified by blood screening and recruited. Blood samples were tested for HBV serologic markers, viral loads, and PCR to identify OBI. HBV full-length genomes were obtained by amplifying two fragments using nested PCR. The characterization of OBI strains was based on sequence analyses compared with HBsAg+ strains obtained from the same donor population. Of the 50 full-length genomes of 172 identified OBI strains, 33 were classified as genotype B (OBI) and 17 strains as genotype C (OBI). Significantly higher nucleotide variabilities were observed in the Pre-S2/S promoter region (SP2) and core upstream regulatory sequence (CURS) in OBI than in their HBsAg+ controls (P < 0.05). Both OBI and OBI showed higher amino acid (aa) variabilities in Pol and Pre-S/S regions than their controls (P < 0.05). In addition, 19 novel OBI-related mutations were found spanning the four open reading frames (ORFs) of the HBV genome. Four novel deletions and one novel insertion were also found in OBI strains. Several novel OBI-related mutations spanning the four ORFs of the virus were identified by characterizing a large sample size of the full-length OBI genome, which may affect the production of HBsAg and contribute to the occult infection of HBV.
在中国,尚未广泛探讨隐匿性乙型肝炎病毒(HBV)感染(OBI)的全长基因组的大样本量特征。通过血液筛查确定 HBsAg 阴性/HBV 核酸检测阳性(HBsAg-/HBV NAT+)的无偿献血者,并招募他们作为研究对象。对血液样本进行 HBV 血清学标志物、病毒载量和 PCR 检测,以确定 OBI。使用巢式 PCR 扩增两个片段获得 HBV 全长基因组。OBI 株的特征基于与从同一供体人群中获得的 HBsAg+株的序列分析。在鉴定的 172 株 OBI 中,有 50 株全长基因组,其中 33 株为 B 基因型(OBI),17 株为 C 基因型(OBI)。在 OBI 中,Pre-S2/S 启动子区域(SP2)和核心上游调控序列(CURS)的核苷酸变异性明显高于其 HBsAg+对照(P<0.05)。与对照相比,OBI 和 OBI 的 Pol 和 Pre-S/S 区域的氨基酸(aa)变异性更高(P<0.05)。此外,在 HBV 基因组的四个开放阅读框(ORF)中发现了 19 个新的 OBI 相关突变。在 OBI 株中还发现了 4 个新的缺失和 1 个新的插入。通过对大量全长 OBI 基因组进行特征分析,确定了跨越病毒四个 ORF 的几个新的 OBI 相关突变,这可能会影响 HBsAg 的产生并导致 HBV 的隐匿性感染。