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Isolation and molecular characterization of Newcastle disease viruses from raptors

机译:猛禽新城疫病毒的分离和分子鉴定

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The present study was undertaken to detect and characterize Newcastle disease virus (NDV) in raptors. Cloacal and oropharyngeal swab samples were collected from 60 casualty raptors during January to March 2009 in Minnesota. Inoculation of all these samples (n=120) in 9-day-old embryonated hens’ eggs resulted in isolation of haemagglutinating viruses in three samples from two bald eagles and one great horned owl. These three haemagglutinating viruses were confirmed as NDV by reverse transcription-polymerase chain reaction (RT-PCR) using fusion gene-specific primers, and were negative for avian influenza virus by RT-PCR. Further characterization revealed that all three possessed 112GKQGRL117 at the fusion gene cleavage site, indicating that they were lentogenic strains. Phylogenetic analysis revealed that all three isolates clustered with published class II genotype II NDVs. The nucleotide sequence homology of the three NDV isolates among themselves was 98.4 to 99.6% and the sequence homology with lentogenic strains from wild birds used for comparison varied between 94.5 and 100%. Detection of NDV strains from raptors merits further epidemiological studies to determine the prevalence of different NDV strains in raptors and their impact in relation to transmission to domestic poultry.
机译:进行本研究以检测和表征猛禽中的新城疫病毒(NDV)。 2009年1月至2009年3月在明尼苏达州从60个伤亡猛禽中收集了泄殖腔和口咽拭子样本。将所有这些样品(n = 120)接种到9天大的胚鸡蛋中,可以分离出来自两只秃鹰和一只大猫头鹰的三个样本中的血凝病毒。使用融合基因特异性引物通过逆转录-聚合酶链反应(RT-PCR)将这三种血凝病毒确认为NDV,而RT-PCR对禽流感病毒呈阴性。进一步的表征表明,这三个在融合基因切割位点均具有 112 GKQGRL 117 ,表明它们是迟发型菌株。系统发育分析表明,所有三个分离株都与已发表的II类基因型II NDV聚集在一起。这三种NDV分离株之间的核苷酸序列同源性为98.4至99.6%,与用于比较的野生鸟类的慢病毒菌株的序列同源性在94.5至100%之间变化。从猛禽中检测NDV毒株值得进一步的流行病学研究,以确定猛禽中不同NDV毒株的流行及其对家禽传播的影响。

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  • 来源
    《Avian Pathology》 |2010年第6期|p.441-445|共5页
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  • 作者单位

    Department of Veterinary Population Medicine;

    Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St Paul, MN, 55108, USA;

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