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在源自大山雀的样本中通过非特异性 DNA 扩增和 PCR 识别和部分基因组特征分析鉴定一种新的腺病毒种。

Recognition and partial genome characterization by non-specific DNA amplification and PCR of a new siadenovirus species in a sample originating from Parus major, a great tit.

机构信息

Veterinary Medical Research Institute, Hungarian Academy of Sciences, P.O. Box 18, H-1581 Budapest, Hungary.

出版信息

J Virol Methods. 2010 Feb;163(2):262-8. doi: 10.1016/j.jviromet.2009.10.007. Epub 2009 Oct 23.

Abstract

A seemingly novel siadenovirus species was detected by PCR and sequencing in the sample of a great tit (Parus major) found dead in Hungary. Since the genus Siadenovirus has very few known members so far, further study of the virus was intriguing not only from epizootiological but also from taxonomical aspects. The sample, which had been tested in another PCR survey previously, consisted of less than 50 microl of extracted nucleic acid. To ensure sufficient target DNA for an extended study, the viral genome had to be preserved. To this end, the sample was subjected to a novel method of non-specific DNA amplification. Using the amplified DNA as target, different PCR and sequencing strategies were applied with consensus or specific primers for the study of the central genome part of the putative tit adenovirus. The sequence of supposedly one half (13,628 bp) of the genome was determined including eight full genes between the genes of the IVa2 and hexon proteins. The gene content of the viral genome fragment as well as the results of the phylogenetic analyses with different proteins confirmed the discovery of a new species in the genus Siadenovirus. This is the first report on the detection of an adenovirus in great tits. The methods, described in this work, proved suitable for the recovery of nucleic acid samples that contain irreplaceable microbial genomic DNA but are only available in limited quantities.

摘要

一种看似新颖的腺病毒物种通过聚合酶链反应(PCR)和测序在匈牙利死亡的大山雀(Parus major)样本中被检测到。由于迄今为止腺病毒属的已知成员非常少,因此不仅从流行病学角度,而且从分类学角度来看,对该病毒的进一步研究非常有趣。该样本之前已经在另一项 PCR 调查中进行了测试,仅包含少于 50 微升的提取核酸。为了确保有足够的目标 DNA 进行扩展研究,必须保存病毒基因组。为此,该样本采用了一种新的非特异性 DNA 扩增方法。使用扩增的 DNA 作为靶标,应用不同的 PCR 和测序策略,使用通用或特定引物研究推定的大山雀腺病毒的中央基因组部分。确定了假定的基因组的一半(13628bp)的序列,包括 IVa2 和六邻体蛋白之间的八个完整基因。病毒基因组片段的基因含量以及不同蛋白质的系统发育分析结果证实了在腺病毒属中发现了一个新物种。这是首次在大山雀中检测到腺病毒的报告。本文中描述的方法证明适用于回收含有不可替代微生物基因组 DNA 但数量有限的核酸样本。

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