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马γ-疱疹病毒DNA包装蛋白基因的检测与核苷酸测序

Detection and nucleotide sequencing of a DNA-packaging protein gene of equine gammaherpesviruses.

作者信息

Kleiboeker Steven B, Turnquist Susan E, Johnson Philip J, Kreeger John M

机构信息

Veterinary Medical Diagnostic Laboratory, Department of Veterinary Pathobiology, University of Missouri, College of Veterinary Medicine, Columbia, MO 65211, USA.

出版信息

J Vet Diagn Invest. 2004 Jan;16(1):67-74. doi: 10.1177/104063870401600112.

Abstract

In previous studies, novel putative viral pathogens designated that asinine herpesvirus 4 (AsHV4) and asinine herpesvirus 5 (AsHV5) were associated with fatal interstitial pneumonia in donkeys (Equus asinus). Nucleotide sequence analysis of a portion of the DNA polymerase gene identified these putative pathogens as herpesviruses and possibly as members of the Gammaherpesvirinae subfamily. Although similar to equine herpesvirus 2 (EHV2) and equine herpesvirus 5 (EHV5), sequence diversity was observed among the detected viruses. In this study, novel sequence is reported for a DNA-packaging protein gene of EHV5 plus AsHV4, AsHV5, and a newly described putative pathogen herein designated asinine herpesvirus 6 (AsHV6). Phylogenetic analysis of these sequences suggested that the equine gammaherpesviruses may form a separate clade within the Gammaherpesvirinae subfamily. Based on the sequence of EHV2 and the novel sequences reported in this study, a PCR assay was developed to detect equine gammaherpesviruses. Products of the predicted size were produced after amplification of DNA from EHV2, EHV5, AsHV4, AsHV5, and AsHV6. This nonnested assay was shown to consistently amplify approximately 10 genomic copies of EHV2. Amplification products were not produced from DNA template of other alpha- and gammaherpesviruses. Because the role of gammaherpesviruses has not been well defined in equine disease, it is envisioned that a single, sensitive PCR assay to detect these potential pathogens will facilitate further assessment of their role in disease.

摘要

在先前的研究中,新发现的假定病毒病原体——驴疱疹病毒4(AsHV4)和驴疱疹病毒5(AsHV5),与驴(马属驴)的致命性间质性肺炎有关。对DNA聚合酶基因部分序列进行核苷酸序列分析后,确定这些假定病原体为疱疹病毒,可能属于γ疱疹病毒亚科成员。尽管与马疱疹病毒2(EHV2)和马疱疹病毒5(EHV5)相似,但在检测到的病毒之间观察到了序列多样性。在本研究中,报告了EHV5以及AsHV4、AsHV5和本文新描述的假定病原体——驴疱疹病毒6(AsHV6)的DNA包装蛋白基因的新序列。对这些序列进行系统发育分析表明,马γ疱疹病毒可能在γ疱疹病毒亚科内形成一个单独的进化枝。基于EHV2的序列以及本研究报告的新序列,开发了一种用于检测马γ疱疹病毒的PCR检测方法。从EHV2、EHV5、AsHV4、AsHV5和AsHV6的DNA扩增后产生了预测大小的产物。该非巢式检测方法显示能持续扩增约10个EHV2基因组拷贝。其他α和γ疱疹病毒的DNA模板未产生扩增产物。由于γ疱疹病毒在马疾病中的作用尚未明确界定,预计一种单一、灵敏的PCR检测方法来检测这些潜在病原体将有助于进一步评估它们在疾病中的作用。

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