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Variability of the S gene of hepatitis B virus in southeastern China

机译:中国东南部乙型肝炎病毒S基因的变异性

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摘要

In a study of 315 HBV specimens obtained from southern China, 240 (76.9%) were assigned to genotype B, 72 (22.9%) were genotype C, two (0.6%) were genotype A and one (0.3%) was genotype D. Statistical analysis revealed that variables such as age, gender, HBV vaccination rate, hepatitis anamnesis rate, anti-HBs and HBeAg prevalence and virus load were insignificant between genotype B (n = 240) and genotype C cases (n = 72) (P > 0.05). However, the frequency of amino acid (aa) substitutions in the major hydrophilic region (MHR; aa 99–169) and the putative HLA class I-restricted cytotoxic T lymphocyte (CTL) epitope region of the S gene, as well as the overlapping polymerase/RT region (aa 32–212), were significantly higher in genotype C group than genotype B (P < 0.001). These results suggest that the higher variability within genotype C carriers may account for the pathogenic potential.
机译:在一项对来自中国南方的315例HBV标本的研究中,将240个(76.9%)归为基因型B,将72个(​​22.9%)归为基因型C,将两个(0.6%)归为基因型A,将一个(0.3%)归为基因型D.统计分析显示,在基因型B(n = 240)和基因型C(n = 72)病例之间,年龄,性别,HBV疫苗接种率,肝炎复诊率,抗HBs和HBeAg患病率和病毒载量等变量无关紧要(P> 0.05)。但是,主要亲水区域(MHR; aa 99–169)和假定的HLA I类限制的细胞毒性T淋巴细胞(CTL)表位区域的氨基酸(aa)取代频率以及重叠基因型C组的聚合酶/ RT区域(aa 32–212)显着高于基因型B(P <0.001)。这些结果表明,基因型C携带者内部较高的变异性可能是造成致病性的潜在原因。

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