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Identification and Genome Characterization of the First Sicinivirus Isolate from Chickens in Mainland China by Using Viral Metagenomics

机译:利用病毒基因组学鉴定和鉴定中国大陆第一批鸡新城疫病毒。

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摘要

Unlike traditional virus isolation and sequencing approaches, sequence-independent amplification based viral metagenomics technique allows one to discover unexpected or novel viruses efficiently while bypassing culturing step. Here we report the discovery of the first Sicinivirus isolate (designated as strain JSY) of picornaviruses from commercial layer chickens in mainland China by using a viral metagenomics technique. This Sicinivirus isolate, which contains a whole genome of 9,797 nucleotides (nt) excluding the poly(A) tail, possesses one of the largest picornavirus genome so far reported, but only shares 88.83% and 82.78% of amino acid sequence identity to that of ChPV1 100C () and Sicinivirus 1 strain UCC001 (), respectively. The complete 939 nt 5′UTR of the isolate strain contains at least twelve stem-loop domains (A–L), representing the highest set of loops reported within Sicinivirus genus. The conserved 'barbell-like' structure was also present in the 272 nt 3′UTR of the isolate as that in the 3′ UTR of Sicinivirus 1 strain UCC001. The 8,586 nt large open reading frame encodes a 2,862 amino acids polyprotein precursor. Moreover, Sicinivirus infection might be widely present in commercial chicken farms in Yancheng region of the Jiangsu Province as evidenced by all the tested stool samples from three different farms being positive (17/17) for Sicinivirus detection. This is the first report on identification of Sicinivirus in commercial layer chickens with a severe clinical disease in mainland China, however, further studies are needed to evaluate the pathogenic potential of this picornavirus in chickens.
机译:与传统的病毒分离和测序方法不同,基于序列独立扩增的病毒宏基因组学技术使人们能够绕开培养步骤,高效发现意想不到的病毒或新型病毒。在这里,我们报告使用病毒宏基因组学技术从中国大陆的商业鸡中发现了微小RNA病毒的第一个Sicinivirus分离株(称为JSY株)。该Sicinivirus分离株包含9797个核苷酸(nt)的全基因组(不包括poly(A)尾巴),是迄今为止报道的最大的微小核糖核酸病毒基因组之一,但与该蛋白的氨基酸序列同一性仅为88.83%和82.78%。 ChPV1 100C()和Sicinivirus 1毒株UCC001()。分离株的完整939 nt 5'UTR包含至少十二个茎环结构域(A–L),代表Sicinivirus属中报道的最高环组。该保守的“杠铃状”结构也存在于该分离株的272 nt 3'UTR中,就像该病毒在Sicinivirus 1株UCC001的3'UTR中一样。 8,586 nt的大型开放阅读框编码2,862个氨基酸的多蛋白前体。此外,在江苏省盐城市地区的商业养鸡场中,可能存在广泛的Sicinivirus感染,这是由来自三个不同农场的所有粪便样本检测到的Sicinivirus检测呈阳性(17/17)所证明的。这是在中国大陆首次鉴定出具有严重临床疾病的商业蛋鸡中的脊髓灰质炎病毒的报道,但是,尚需要进一步的研究来评估这种微小RNA病毒在鸡中的致病潜力。

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