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首页> 外文期刊>Transboundary and emerging diseases >Characterization of a Novel Chimeric Swine Enteric Coronavirus from Diseased Pigs in Central Eastern Europe in 2016
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Characterization of a Novel Chimeric Swine Enteric Coronavirus from Diseased Pigs in Central Eastern Europe in 2016

机译:2016年东欧中部患病猪的新型嵌合猪肠道冠状病毒的特征分析

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摘要

During a severe outbreak of diarrhoea and vomiting in a pig herd in Central Eastern Europe, faecal samples were tested positive for porcine epidemic diarrhoea virus (PEDV) and negative for transmissible gastroenteritis virus (TGEV) using a commercial RT-qPCR assay that can detect both of these coronaviruses. However, further analyses, using other TGEV-and PEDV-specific RT-qPCR assays, provided results inconsistent with infection by either of these viruses. Sequencing of an amplicon (ca. 1.6 kb), generated by an RT-PCR specific for the PEDV S-gene, indicated a very close similarity (ca. 99% identity) to recently described chimeric viruses termed swine enteric coronaviruses (SeCoVs). These viruses (with an RNA genome of ca. 28 kb) were first identified in Italy in samples from 2009 but have not been detected there since 2012. A closely related virus was detected in archived samples in Germany from 2012, but has not been detected subsequently. Building on the initial sequence data, further amplicons were generated and over 9 kb of sequence corresponding to the 30-terminus of the new SeCoV genome was determined. Sequence comparisons showed that the three known SeCoVs are >= 98% identical across this region and contain the S-gene and 3a sequences from PEDV within a backbone of TGEV, but the viruses are clearly distinct from each other. It is demonstrated, for the first time, that pigs from within the SeCoV-infected herd seroconverted against PEDV but tested negative in a TGEV-specific ELISA that detects antibodies against the S protein. These results indicate that SeCoV is continuing to circulate in Europe and suggest it can cause a disease that is very similar to PED. Specific detection of the chimeric SeCoVs either requires development of a new diagnostic RT-qPCR assay or the combined use of assays targeting the PEDV S-gene and another part of the TGEV genome.
机译:在东欧中部猪群腹泻和呕吐的严重暴发期间,粪便样品使用商业RT-qPCR检测方法检测猪流行性腹泻病毒(PEDV)阳性,而传播性肠胃炎病毒(TGEV)阴性,这些冠状病毒。但是,使用其他TGEV和PEDV特异性RT-qPCR分析进行的进一步分析提供的结果与这些病毒中的任一种感染都不符。通过对PEDV S基因特异的RT-PCR生成的扩增子(约1.6 kb)测序,与最近描述的称为猪肠冠状病毒(SeCoVs)的嵌合病毒非常相似(约99%一致性)。这些病毒(具有大约28 kb的RNA基因组病毒)最早于2009年在意大利的样本中发现,但自2012年以来在意大利未发现。从2012年起在德国的存档样本中发现了密切相关的病毒,但尚未发现后来。基于初始序列数据,产生了更多的扩增子,并确定了超过9 kb的序列,该序列对应于新SeCoV基因组的30末端。序列比较显示,三个已知的SeCoV在该区域内> = 98%相同,并在TGEV的骨架内包含来自PEDV的S基因和3a序列,但这些病毒显然彼此不同。首次证明,来自SeCoV感染的猪群中的猪已针对PEDV进行血清转化,但在TGEV特异性ELISA中检测为阴性,该ELISA检测到针对S蛋白的抗体。这些结果表明,SeCoV在欧洲继续流行,并暗示它可能导致与PED非常相似的疾病。嵌合SeCoV的特异性检测要么需要开发新的诊断性RT-qPCR检测方法,要么需要结合使用针对PEDV S基因和TGEV基因组另一部分的检测方法。

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