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固定剂类型和固定时间对石蜡包埋绵羊肺样本中梅迪-维斯纳病毒PCR检测及免疫组化检测的影响

Effects of fixative type and fixation time on the detection of Maedi Visna virus by PCR and immunohistochemistry in paraffin-embedded ovine lung samples.

作者信息

Benavides Julio, García-Pariente Carlos, Gelmetti Daniela, Fuertes Miguel, Ferreras María Carmen, García-Marín Juan Francisco, Pérez Valentín

机构信息

Departamento de Patología Animal: Medicina Animal (Anatomía Patológica), Facultad de Veterinaria, Universidad de León, Campus de Vegazana s/n, 24071 León, Spain.

出版信息

J Virol Methods. 2006 Nov;137(2):317-24. doi: 10.1016/j.jviromet.2006.07.009. Epub 2006 Aug 14.

DOI:10.1016/j.jviromet.2006.07.009
PMID:16908077
Abstract

In doubtful cases, the histopathological diagnosis of lesions induced by Maedi Visna virus (MVV), a chronic multisystemic lentiviral disease of sheep, needs to be confirmed by the demonstration of MVV in the tissues. The influence of fixatives and the duration of fixation on the detection of MVV by immunohistochemistry (IHC) and PCR in paraffin-embedded tissues was assessed in lung samples with lesions in different degree, from five sheep serologically positive. Samples were fixed in 10% neutral buffered formalin (NBF), Bouin's solution (BS) and a zinc salts-based fixative (ZSF), for different periods of time between 24 h and 30 days. The three fixatives preserved the morphology of the tissues, although in ZSF-fixed samples an increase in the number of desquamated cells was seen in the alveoli. Tissues showed a similar degree of immunolabelling, irrespective of the duration of fixation using ZSF and NBF fixatives. MVV nucleic acids could be detected in samples fixed up to 14 days in NBF and 30 days in ZSF. However, in BS fixed tissues, immunostaining was weak and non-specific signals were observed after 4 days of fixation. Amplification of proviral DNA could not be obtained by PCR in these samples. IHC detected viral antigens in all sheep whereas one sheep with mild lesions was always negative by PCR.

摘要

在可疑病例中,梅迪 - 维斯纳病毒(MVV)引起的病变的组织病理学诊断需要通过在组织中检测到MVV来确认,MVV是绵羊的一种慢性多系统慢病毒病。在来自五只血清学阳性绵羊的不同程度病变的肺样本中,评估了固定剂和固定时间对石蜡包埋组织中通过免疫组织化学(IHC)和聚合酶链反应(PCR)检测MVV的影响。样本分别用10%中性缓冲福尔马林(NBF)、波因氏液(BS)和一种锌盐基固定剂(ZSF)在24小时至30天的不同时间段进行固定。尽管在ZSF固定的样本中肺泡内脱落细胞数量增加,但这三种固定剂均保留了组织的形态。无论使用ZSF和NBF固定剂的固定时间长短,组织的免疫标记程度相似。在NBF中固定长达14天和在ZSF中固定30天的样本中均可检测到MVV核酸。然而,在BS固定的组织中,固定4天后免疫染色较弱且观察到非特异性信号。在这些样本中通过PCR无法获得前病毒DNA的扩增。免疫组织化学在所有绵羊中均检测到病毒抗原,而一只病变较轻的绵羊通过PCR检测始终为阴性。

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