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Development of nested RT-PCR for the detection of swine hepatitis E virus in formalin-fixed, paraffin-embedded tissues and comparison with in situ hybridization

机译:巢式RT-PCR技术在福尔马林固定石蜡包埋组织中检测猪戊型肝炎病毒的研究及与原位杂交的比较

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Swine hepatitis E virus (HEV) was detected in formalin-fixed, paraffin-embedded tissues from naturally infected pigs by nested reverse transcription-polymerase chain reaction (RT-PCR). The results for seminested RT-PCR were compared with those determined by in situ hybridization. The results obtained show that use of xylene deparaffinization, digestion with proteinase K followed by nested RT-PCR is a reliable detection method. Swine HEV nucleic acid was detected in formalin-fixed, paraffin-embedded hepatic tissues from 40 pigs. Distinct positive signals for swine HEV were obtained in the same hepatic tissues by in situ hybridization. Swine HEV nucleic acid was localized to the cytoplasm of hepatocytes and had a granular staining pattern. The rate of agreement between nested RT-PCR and in situ hybridization for the detection of swine HEV in formalin-fixed, paraffin-embedded hepatic tissues was 100%
机译:通过巢式逆转录-聚合酶链反应(RT-PCR)在来自自然感染猪的福尔马林固定的石蜡包埋组织中检测到猪戊型肝炎病毒(HEV)。将半巢式RT-PCR的结果与通过原位杂交确定的结果进行比较。获得的结果表明,使用二甲苯去石蜡,用蛋白酶K消化,然后进行嵌套式RT-PCR是一种可靠的检测方法。在来自40头猪的福尔马林固定石蜡包埋的肝组织中检测到猪HEV核酸。通过原位杂交在相同的肝组织中获得猪戊型肝炎病毒的不同阳性信号。猪HEV核酸位于肝细胞的细胞质中,并具有颗粒状染色模式。巢式RT-PCR与原位杂交在福尔马林固定石蜡包埋的肝组织中检测猪HEV的一致性率为100%

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