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作 者:刘凌芝[1] 郭傅佳 魏可慧 乔乔 叶舒慧 辛思明[1] 郑九生[1] 刘金辉 Liu Lingzhi;Guo Fujia;Wei Kehui(Maternal and Infantile Hospital of Jiangxi Province,Nanchang 330006;Department of Laboratory Medicine of College of Public Medcine,Medical School of Nanchang University,Nanchang 330006;Department of Medical Microbiology,Medical College of Nanchang University,Nanchang 330006)
机构地区:[1]江西省妇幼保健院,南昌330006 [2]南昌大学医学部公共卫生学院检验医学专业,南昌330006 [3]南昌大学医学部微生物学教研室,南昌330006
出 处:《现代妇产科进展》2018年第8期580-583,共4页Progress in Obstetrics and Gynecology
基 金:江西省科技厅科技支撑计划(No:20151BBG70101); 南昌大学大学生创新创业训练项目(2017年)
摘 要:目的:调查江西地区待产孕妇慢性感染的HBV表面抗原"α"抗原决定簇变异特征,探讨HBV母婴传播相关的病毒因素。方法:产前24~48h,收集3948例待产孕妇血清,酶免疫法筛查HBV感染者。抽提HBV阳性血清HBV DNA,PCR扩增HBV S基因并测序。应用Clustal X和Bioedit软件将不同感染者的HBV S基因核苷酸与参考序列进行多重比对,分析"α"抗原决定簇的变异与HBV血清型。在线genotyping软件分析感染的HBV基因型。结果:3948例检测出178例HBV阳性标本,从146例血清标本中成功扩增出HBV S基因,112例感染B基因型HBV,属于adw亚型,感染率为76.71%;34例感染C基因型HBV,属于adr亚型,感染率为23.29%,B基因型和C基因型HBV的感染率存在显著差异(P<0.001)。18例S基因序列上检测到"α"抗原决定簇有突变(突变率12.33%),突变分为7种类型,5例T126A、2例P127T/S、2例Q129H/R、2例M132L、3例T140/I、1例T143M和3例G145R。B和C基因型HBV"α"抗原决定簇突变率和"α"抗原决定簇双环之间的突变率无显著差异(P>0.05)。结论:江西地区孕妇感染的B和C基因型HBV及其"α"抗原决定簇的点突变可能是致母婴传播高度相关的病毒因素。Objective: Mutation characteristics of"α"antigenic determinant of Heptitis B virus infecting puerpera women in Jiangxi Province was analyzed with an aim to prevent HBV maternal-infant transmission efficiently. Methods: The sera of 3948 puerpera women were collected for detection of HBV infection.HBV DNA was extracted for amplification of HBV S gene.The positive amplicons were sequenced for analysis of HBV genotypes. Clustal X and Bioedit software were used to align the sequence of S gene to analyze the mutation sites within "α"antigenic determinant.Results: 178 cases of positive HBV sera were detected from 3948 sera samples.146 positive amplicons were amplified.112 cases were infected with genotype B HBV( adw subtype) with infection rate of 76.71% and 34 cases were infected with genotype C HBV( adw subtype) with infection rate of 23.29%.The infection rate of both genotype B and C was statistically different( P〈0.001).The mutation sites within "α"antigenic determinant were detected in 18 cases with mutaion rate of 12. 33%. 7 types of mutation were found to be 5 cases of T126 A、2 cass of P127 T/S、2 cases of Q129 H/R、2 cass of M132 L、3 cass of T140/I、1 cases of T143 M and 3 cases of G145 R.The mutation sites within "α"antigenic determinant of genotype B and C as well as on the both loops of "α"antigenic determinant were found to be no statistically significant different( P〉 0.05). Conclusions: The mutation sites within "α"antigenic determinant of HBV infecting puerpera women in Jiangxi Province occurred mainly in genotype B and C HBV.The prevance of HBV mutants with high frequency of specific mutation site within"α"antigenic determinant was not found.Genotype B and C and site mutations within"α"antigenic determinant of HBV may be the high risk factors associated with HBV maternal-infant transmission.
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