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Sequence analysis of the Pre-S gene in chronic asymptomatic HBV carriers with low-level HBsAg

机译:慢性无症状HBsAg低水平无症状HBV携带者Pre-S基因的序列分析

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In a hepatitis B virus (HBV)?infected population, persistently low expression levels of serum HBV serum antigen (HBsAg) are present, particularly in chronic asymptomatic HBV carriers (ASCs). The present study sequenced the HBV Pre?S gene, and aimed to elucidate its features in ASCs with low HBsAg expression compared with in the established HBV Pre?S reference gene sequences from ASCs with high HBsAg expression. A total of 1,308?ASCs were grouped according to HBsAg serum levels (cut?off value, 10?IU/ml), and clinical characteristics were analyzed in detail. The HBV Pre?S gene was sequenced in 276 ASCs with low?level HBsAg; in addition, 100 of the remaining 1,032?ASCs with high?level HBsAg were randomly selected for HBV Pre?S gene sequencing on the basis of age matching with the low?level HBsAg group. Comparative analysis of the gene sequences from these groups was subsequently conducted. The major clinical features of the population with low?level HBsAg were as follows: Most were ASCs with chronic HBV infection; 97.1% were HBsAg/anti?HBe/anti?HBc?positive; 82.54% carried the B?genotype; and 84.13% displayed the adw serotype. The results indicated that there were novel and meaningful mutations, including co?mutations, at numerous loci and sites in the Pre?S gene, as well as deletion mutations in the Pre?S2 gene. These mutations in the Pre?S1 and Pre?S2 gene fragments accounted for 65.38% (68/104) of the 104 B genotype cases in the low?level HBsAg group and 90.91% (20/22) of the 22?C?genotype cases in the low?level HBsAg group, respectively. In conclusion, Pre?S gene mutations may be associated with HBV replication defects, which may be the cause of the observed low expression levels of HBsAg.
机译:在感染了乙肝病毒(HBV)的人群中,血清HBV血清抗原(HBsAg)的表达水平持续低下,尤其是在慢性无症状HBV携带者(ASC)中。本研究对HBV Pre?S基因进行了测序,旨在阐明其在HBsAg低表达的ASC中的特征,与已建立的从HBsAg高表达的ASC的HBV Pre?S参考基因序列相比。根据HBsAg血清水平(截止值,10?IU / ml)将1,308?ASCs分组,并详细分析其临床特征。在276例HBsAg低水平的ASC中对HBV Pre?S基因进行了测序。此外,根据与低水平HBsAg组匹配的年龄,在剩余的1032个高水平HBsAg的ASC中随机选择100个进行HBV Pre?S基因测序。随后对来自这些组的基因序列进行了比较分析。低水平HBsAg人群的主要临床特征如下:大多数为慢性HBV感染的ASC。 HBsAg /抗?HBe /抗?HBc?阳性率为97.1%; 82.54%携带B?基因型; 84.13%的人表现出adw血清型。结果表明,在Pre?S基因的许多位点和位点存在新颖而有意义的突变,包括共突变,以及在Pre?S2基因中的缺失突变。 Pre?S1和Pre?S2基因片段中的这些突变占低水平HBsAg组104 B基因型病例的65.38%(68/104)和22?Cα基因型90.91%(20/22)。低水平HBsAg组的病例。总之,Pre?S基因突变可能与HBV复制缺陷有关,这可能是观察到的HBsAg低表达水平的原因。

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