首页> 外文期刊>The Journal of Veterinary Medical Science >Occurrence of bovine ephemeral fever in Okinawa Prefecture, Japan, in 2012 and development of a reverse-transcription polymerase chain reaction assay to detect bovine ephemeral fever virus gene
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Occurrence of bovine ephemeral fever in Okinawa Prefecture, Japan, in 2012 and development of a reverse-transcription polymerase chain reaction assay to detect bovine ephemeral fever virus gene

机译:2012年,日本冲绳县发生了牛短暂性发热,并开发了一种逆转录聚合酶链反应法以检测牛短暂性发热病毒基因

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References(20) Cited-By(4) In September 2012, several cows and a calf showed decreased activity, anorexia and fever on Ishigaki Island, Okinawa Prefecture, Japan, and the cases were diagnosed as bovine ephemeral fever (BEF). We isolated BEF virus (BEFV) from one of the affected cows and then determined the complete genome sequence of the G gene, which encodes a class I transmembrane glycoprotein of BEFV. The BEFV isolate in this case, ON-3/E/12, was sorted into the same cluster as other BEFV isolates in Japan, Taiwan and China obtained in 1996?2004 and was most closely related to a 2002 Chinese isolate, JT02L, according to the phylogenetic analysis of the complete G gene. Since inactivated vaccines for BEF available in Japan are considered effective against the ON-3/E/12 isolate as well as other isolates in East Asia from 1996?2004, annual vaccination should be conducted to prevent BEF in Okinawa. Additionally, in this study, we developed an RT-PCR assay to detect the BEFV gene in Japan and neighboring countries. Our assay was able to amplify target sequences in all of the tested BEFV isolates, including 18 isolates in Japan and another isolate in Australia. The assay was found to be useful also for testing RNA samples extracted from bovine peripheral blood mononuclear cells, and the detection limit of the assay was 10 copies per tube. We believe that our assay would be an important tool for the screening of BEFV infection and the diagnosis of BEF.
机译:参考文献(20)被引用(4)2012年9月,日本冲绳县石垣岛上几头牛和一头小牛表现出活动减少,厌食和发烧,这些病例被诊断为牛短暂性发热(BEF)。我们从一头受影响的母牛中分离出BEF病毒(BEFV),然后确定了G基因的完整基因组序列,该基因编码BEFV的I类跨膜糖蛋白。在这种情况下,BEFV分离株ON-3 / E / 12与1996、2004和2004、2004年在日本,台湾和中国获得的其他BEFV分离株归为同一类,与2002年的中国分离株JT02L最为相关完整G基因的系统发育分析。由于从1996年至2004年,日本可买到的BEF灭活疫苗被认为对ON-3 / E / 12分离株以及东亚的其他分离株有效,因此应在冲绳县进行年度疫苗接种以预防BEF。此外,在这项研究中,我们开发了一种RT-PCR分析法来检测日本及周边国家的BEFV基因。我们的测定能够扩增所有测试的BEFV分离株中的靶序列,包括日本的18个分离株和澳大利亚的另一个分离株。发现该测定法也可用于测试从牛外周血单核细胞提取的RNA样品,并且该测定法的检测极限是每管10个拷贝。我们相信我们的检测方法将成为筛选BEFV感染和诊断BEF的重要工具。

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