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作 者:周翔天[1,2] 吕茹[1,2] 郑吉顺[3] 陈国胜[1,2] 刘艳艳[1,2] 叶英[1,2] 李家斌[1,2]
机构地区:[1]安徽医科大学第一附属医院感染科,合肥230022 [2]安徽省细菌耐药监控中心,合肥230022 [3]合肥市第一人民医院,合肥230012
出 处:《安徽医科大学学报》2014年第10期1510-1513,共4页Acta Universitatis Medicinalis Anhui
基 金:国家自然科学基金项目(编号:81172737)
摘 要:采集50例乙型肝炎未并发消化道出血患者的血液和粪便标本,采用酶联免疫法检测粪便和血清中乙肝病毒标志物(HBVM),QIAmp DNA Stool kit试剂盒法提取粪便总DNA,巢式PCR定性检测粪便中乙肝病毒DNA(HBVDNA),实时荧光定量PCR(FQ-PCR)定量检测血清和粪便中HBV-DNA。根据血清HBVM阳性的不同组合(感染模式)将50例患者分成3组,粪便乙肝表面抗原(HBsAg)阳性37例,血清HBsAg阳性46例,两者检出率差异有统计学意义(P<0.05),1例血清阴性者,粪便中HBsAg阳性。FQ-PCR定量检测血清和粪便HBV-DNA含量分别为4.35±1.49和4.50±1.59。血清HBV-DNA检测,30例阳性(60%),粪便中HBV-DNA共检测出31例阳性(62%)。We collected the samples offeces and serum for all patients. HBVM in serum and feces were determined with ELISA. Using QIAmp DNA Stool kit to extract human fecal DNA. FQ-PCR were utilized for analysis the content of HBV-DNA in feces and serum while it was detected qualitatively by nested-PCR. Depending on the combination of HBVM, 50 patients were divided into three groups. Hepatitis B surface antigen was positive in 37 cases of stool and 46 cases of serum, both the detection rates were significant ( P 〈0.05 ) . FQ-PCR quantitative detection of HBV-DNA in serum and fecal contents were 4.35 ±1.49 and 4.50 ±1.59 . The positive rates of HBsAg were 74%, 92% in feces and serum, respectively. HBsAg was found in feces in one patient without HBsAg in serum. In 50 patients,the positive rates of HBV-DNA were 62%, 60% in feces and serum,respectively.
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