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使用实时聚合酶链反应对自然感染鸽子的血清、血液、精液和不同组织中的鸽圆环病毒进行定量分析。

Quantification of pigeon circovirus in serum, blood, semen and different tissues of naturally infected pigeons using a real-time polymerase chain reaction.

作者信息

Duchatel J P, Todd D, Willeman C, Losson B

机构信息

Faculty of Veterinary Medicine, Department of Infections and Parasitic Diseases, University of Liège, Liège, Belgium.

出版信息

Avian Pathol. 2009 Apr;38(2):143-8. doi: 10.1080/03079450902737805.

Abstract

The development of a real-time polymerase chain reaction (PCR) based on SYBR Green chemistry is described for the quantification of pigeon circovirus (PiCV) DNA in various samples. Plasmid containing a fragment of the PiCV genome was used to create a standard curve and to estimate the viral DNA copies in analysed samples. Both primers were designed in highly conserved regions to avoid false negatives, and amplified a 139-base-pair amplicon. When the amplifications were performed in the presence of cellular DNA extracted from PCR-negative liver, bursa and spleen samples, the detection limits were respectively 20, 20 and 60 copies of genome per milligram of tissue. These limits were 10, 160 and 25 copies/microl for control blood, sera and semen, respectively. For cloacal swab, the detection limit was 200 copies. The assay showed a linear detection over a six-log range (R(2)>0.99) and displayed reliable inter-assay and intra-assay reproducibility. Application of the test to sera samples indicated the presence of the virus in Belgium in 1991, 6 years before PiCV infections were histologically diagnosed. Testing of samples from pigeons with "young pigeon sickness" showed that the viral loads were high in the bursa of Fabricius (up to 2.07 x 10(9) copies/mg), the liver (up to 2.88 x 10(8) copies/mg) and spleen (up to 5.57 x 10(8) copies/mg). For liver, the viral load was significantly higher in sick pigeons than in apparently healthy pigeons. Detection of high quantities of PiCV DNA (up to 1.6 x 10(9) copies/microl) in the sera or blood of some young healthy pigeons indicated that the viral load in this sample type would not be useful as predictive indicator of disease. This work also showed that PiCV DNA can be detected in relatively large amounts in semen (up to 1.0 x 10(7) copies/ejaculate) and cloacal swabs (up to 3.6 x 10(10) copies/swab), confirming that PiCV may be transmitted by vertical and horizontal routes.

摘要

本文描述了一种基于SYBR Green化学的实时聚合酶链反应(PCR)方法,用于定量检测各种样本中的鸽圆环病毒(PiCV)DNA。使用含有PiCV基因组片段的质粒构建标准曲线,并估算分析样本中的病毒DNA拷贝数。两条引物均设计在高度保守区域,以避免假阴性,扩增出一个139碱基对的扩增子。当在从PCR阴性的肝脏、法氏囊和脾脏样本中提取的细胞DNA存在下进行扩增时,每毫克组织的检测限分别为20、20和60个基因组拷贝。对照血液、血清和精液的检测限分别为10、160和25拷贝/微升。泄殖腔拭子的检测限为200拷贝。该检测方法在六个对数范围内呈线性检测(R(2)>0.99),并显示出可靠的批间和批内重复性。将该检测方法应用于血清样本表明,在1991年比利时就已存在该病毒,比PiCV感染的组织学诊断早6年。对患有“幼鸽病”的鸽子样本进行检测表明,法氏囊中病毒载量很高(高达2.07 x 10(9)拷贝/毫克),肝脏(高达2.88 x 10(8)拷贝/毫克)和脾脏(高达5.57 x 10(8)拷贝/毫克)。对于肝脏,患病鸽子的病毒载量明显高于看似健康的鸽子。在一些年轻健康鸽子的血清或血液中检测到大量的PiCV DNA(高达1.6 x 10(9)拷贝/微升),表明该样本类型中的病毒载量不能作为疾病的预测指标。这项工作还表明,在精液(高达1.0 x 10(7)拷贝/射精)和泄殖腔拭子(高达3.6 x 10(10)拷贝/拭子)中可以检测到相对大量的PiCV DNA,证实PiCV可能通过垂直和水平途径传播。

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