Department of Health and Applied Sciences, Nairobi Technical Training Institute, Nairobi, Kenya.
Department of Medical Laboratory Science, Kenyatta University, Nairobi, Kenya.
Virol J. 2020 Nov 13;17(1):176. doi: 10.1186/s12985-020-01447-2.
Hepatitis B virus (HBV) causes significant morbidity and mortality globally primarily due to its ability to cause hepatitis, liver cirrhosis and hepatocellular carcinoma. The Kenya National Blood Transfusion Services screens for Hepatitis B antibodies using the chemiluminescent microparticle immunoassay method. This test does not inform on the genotypic characteristics of the virus or the actual presence of the virus in blood. This study therefore sought to determine the serologic and genotypic profiles of HBV circulating among the voluntary blood donors in Nairobi.
Blood samples were collected in plain and EDTA vacutainers and tested for the Hepatitis B surface antigen (HBsAg). HBV DNA was then extracted from plasma, its overlapping P/S gene amplified and sequenced. The resulting sequences were used to analyze for the circulating genotypes and mutations within the P and S genes. Bivariate statistical analysis was used to determine the association between demographic factors and HBV infection.
A seroprevalence of 2.3% (n = 7) was reported. The age group 19-28 years was significantly associated with HBV infection. Nine samples were positive for HBV DNA; these included 2 HBsAg positive samples and 7 HBsAg negative samples. Genotype A, sub genotype A1 was found to be exclusively prevalent while a number of mutations were reported in the "a" determinant segment of the major hydrophilic region of the S gene associated with antibody escape. RT mutations including mutation rt181T in the P gene conferring resistance against Lamivudine and other ʟ-nucleoside drugs were detected.
There is a high prevalence of occult HBV infections among these blood donors and therefore the testing platform currently in use requires revision.
乙型肝炎病毒(HBV)在全球范围内造成了大量的发病率和死亡率,主要是因为它能够引起肝炎、肝硬化和肝细胞癌。肯尼亚国家血液服务中心使用化学发光微粒子免疫分析方法筛查乙型肝炎抗体。该测试无法告知病毒的基因型特征或血液中病毒的实际存在。因此,本研究旨在确定内罗毕自愿献血者中循环的乙型肝炎病毒的血清学和基因型特征。
采集普通和 EDTA 真空采血管中的血液样本,检测乙型肝炎表面抗原(HBsAg)。然后从血浆中提取 HBV DNA,对其重叠的 P/S 基因进行扩增和测序。所得序列用于分析循环基因型和 P 和 S 基因内的突变。使用双变量统计分析来确定人口统计学因素与 HBV 感染之间的关联。
报告了 2.3%(n=7)的血清流行率。19-28 岁年龄组与 HBV 感染显著相关。有 9 个样本 HBV DNA 阳性;其中包括 2 个 HBsAg 阳性样本和 7 个 HBsAg 阴性样本。发现仅存在基因型 A,亚基因型 A1,同时在 S 基因主要亲水区域的“a”决定簇中报告了一些与抗体逃逸相关的突变。逆转录酶突变,包括 P 基因中的突变 rt181T,赋予对拉米夫定和其他 ʟ-核苷药物的耐药性。
这些献血者中存在大量隐匿性 HBV 感染,因此目前使用的检测平台需要修订。