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作 者:曹虹[1] 郭辉玉[1] 卓礼梅[1] 张文炳[1]
机构地区:[1]第一军医大学微生物学教研室,中山医科大学微生物学教研室
出 处:《第一军医大学学报》1996年第1期17-19,共3页Journal of First Military Medical University
基 金:美国中华医学基金
摘 要:用聚合酶链式反应(PCR)法检测了7例胎儿的12份组织标本,在4份脑组织和1份脾组织中扩增出700bp片段,经酶切鉴定证明其为特异性片段。用地高辛标记的人微小病毒B19(PVB19)DNA探针对PCR检测阳性标本进行原位杂交,在2份脑组织和1份脾组织中检出了PVB19DNA阳性颗粒,PCR和原位杂交方法结合应用可为胎儿PVB19感染的病原学诊断和致病机理的研究提供一套持异、敏感和准确的实验方法。Attempts were made to detect human parvovirus B19 DNA by PCR and in situ hybridization in fetal tissues from 7 fetuses,Parvovirus B19 DNA:sequences were detected by PCR and positive results wereobtained in 4 samples of brain tissue and 1 of spleen tissue from these fetuses,In situ hybridization withDigoxigenin- labelled probe for human parvovirus B19 was performed on formalin-fixed paraffin-embeddedtissues from these fetuses,Parvovirus;DNA could be detected precisely and localized mainly in the nuclei ofImmature hematopoetic cells within fetal blood vessels, PCR and in situ bybridization were established to provide specific,sensitive and accurate methods for pathologic diagbosis and pathogenecity study of par-vovirus B19、
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