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Genetic variability in the precore and core promoter regions of hepatitis B virus strains in Karachi

机译:卡拉奇乙型肝炎病毒株前核心和核心启动子区域的遗传变异

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Background Hepatitis B virus (HBV) genotypes have distinct geographic distribution. Moreover, much genetic variability has been described in the precore (PC) and basal core promoter (BCP) regions of the HBV genome. The local prevalence of HBV genotypes and mutations has not been well studied. The aim of the present study is to determine the prevalence of HBV genotypes and mutations in the PC and BCP region in HBV strains in Karachi. Methods A total of 109 chronic hepatitis B patients with detectable HBV DNA by a PCR assay were enrolled in the study. Sera were tested for HBeAg, anti-HBe antibody and liver profile. HBV genotypes and mutations in the PC and BCP regions were detected by INNO-LiPA line-probe assays. Results Of the 109 patients investigated, 38 (35%) were HBeAg positive while 71 (65%) were HBeAg negative. Genotype D was present in 100% of the patients. Two patients had co-infection with genotype A. There was no significant difference in the baseline characteristics, mean ALT levels, and presence of clinical cirrhosis in patients with HBeAg positive or negative strains with or without PC and BCP mutations. Of the 38 HBeAg positive patients, 9 (24%) had PC and BCP mutations. In the HBeAg negative patient group, mutations were detected in 44 (62%) of the strains investigated. More than one mutation was common, seen in 26 (37%) patients with HBeAg negative disease and 6 (16%) patients with HBeAg positive disease. Twelve (17%) HBeAg negative patients had dual T1762 and A1764 mutations. None of the HBeAg positive patients had T1762 mutation. Mutations were undetectable in 27 (38%) of patients with HBeAg negative disease. Conclusion Our study shows that type D is the main HBV genotype in Karachi, Pakistan. Significant numbers of patients infected with this genotype have PC and BCP variants. Mutations at more than one site are common. Patients harboring these mutants do not differ significantly in their clinical presentation from patients having wild type infection.
机译:背景乙型肝炎病毒(HBV)基因型具有明显的地理分布。此外,已在HBV基因组的前核(PC)和基底核心启动子(BCP)区描述了许多遗传变异。 HBV基因型和突变的局部患病率尚未得到很好的研究。本研究的目的是确定卡拉奇HBV株中HBV基因型和PC和BCP区域中的突变发生率。方法总共109例经PCR检测可检测到的HBV DNA的慢性乙型肝炎患者。测试血清的HBeAg,抗HBe抗体和肝功能。通过INNO-LiPA线探针测定法检测了PC和BCP区的HBV基因型和突变。结果在所调查的109例患者中,HBeAg阳性38例(35%),HBeAg阴性71例(65%)。基因型D存在于100%的患者中。两名患者同时感染了A型基因。HBeAg阳性或阴性菌株(无论是否患有PC和BCP突变)的基线特征,平均ALT水平以及临床肝硬化的发生率均无显着差异。在38例HBeAg阳性患者中,有9例(24%)具有PC和BCP突变。在HBeAg阴性患者组中,在所调查的菌株中有44个(62%)检测到突变。在26个(37%)HBeAg阴性疾病患者和6个(16%)HBeAg阳性疾病患者中发现了不止一种突变。十二名(17%)HBeAg阴性患者具有双重T1762和A1764突变。 HBeAg阳性患者均无T1762突变。在HBeAg阴性疾病的27例患者中检测不到突变(38%)。结论我们的研究表明D型是巴基斯坦卡拉奇的主要HBV基因型。大量感染该基因型的患者患有PC和BCP变异。一个以上位点的突变很常见。携带这些突变体的患者在临床表现上与野生型感染患者无明显差异。

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