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作 者:孔健[1] 李宇静[1] 章美云[1] 徐爱强[1] 迮文远[1]
出 处:《中国计划免疫》1996年第3期120-123,共4页Chinese Journal of Vaccines and Immunization
摘 要:用一对选自脊髓灰质炎病毒及一对由Hyypia所设计的细小RNA病毒核酸5’端非编码区的引物,逆转录并扩增脊髓灰质炎病毒及其它肠道病毒的核酸,从而把脊髓灰质炎病毒和其它非脊髓灰质炎肠道病毒进行鉴别。105份被血清中和试验定型为脊髓灰质炎病毒的标本,逆转录一聚合酶链反应(RT─PCR)的结果亦定为脊髓灰质炎病毒,灵敏度为1m%;133份被血清中和试验定为非脊髓灰质炎肠道病毒的标本,均被判定为非脊髓灰质炎病毒,特异度为100%。该方法可用于脊髓灰质炎病毒的检测及脊髓灰质炎病毒与其它非脊髓灰质炎肠道病毒的鉴别。or rapid distinguishing of polioviruses from other nonpolio-enteroviruses isolated from clini-cal specimens,a protocal was developed using a pair of primers selected from the conserved 5'noncoding region of the poliovirus genome and a pair of human picomavirus primers reported byHyypia.105 virus strains which were identified as polioviruses by tissue culture seroneutralizationtest were positive by polio-specific RT-PCR,the sensitivity was 100%.Of the 133 virus strainsidentified as nonpolio-enteroviruses by tissue culture seroneutmlizing test,no amplified productswere detected by polio-spndic RT-PCR,the specificity was 100%.It allowr for the detection ofpolioviruses and for distinguisiug then from nonpolio-enteroviruses.
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