Department of Parasitology and Animal Diseases, Veterinary Research Division, National Research Centre, P.O. Box 12622, 33 El-Tahrir Street, Dokki, Giza, Egypt.
Res Vet Sci. 2010 Oct;89(2):290-4. doi: 10.1016/j.rvsc.2010.02.019. Epub 2010 Mar 20.
Orf virus was clinically diagnosed from different field cases of sheep and goat in Hawamdia, Giza, Egypt during the summer 2006. Skin scabs were collected and used for virus isolation, electron microscopy, PCR and sequencing for confirmation, and differential diagnosis. The aetiological virus was fruitfully isolated on the chorio-allantoic membrane of SPF embryonated chicken eggs indicated by expressing the characteristic pock lesions of Poxviridae family. Electron microscopy examination exposed negatively stained oval-shape virus particles trait for members of the genus Parapoxvirus. A 392 bp fragment of the late transcription factor (VLTF-1) gene of orf virus was amplified by PCR from the DNA extracted from the isolates. Phylogenetic analysis revealed 99% identity with other orf virus strains reported worldwide. Selection and processing of clinical specimens and PCR assay applied in this endeavor, presented a reliable laboratory diagnostic tool for orf infections and first molecular characterization of Egyptian orf isolates.
2006 年夏季,在埃及吉萨的 Hawamdia,从不同绵羊和山羊的野外病例中临床诊断出了羊口疮病毒。采集皮肤结痂物用于病毒分离、电子显微镜检查、PCR 和测序以确认和进行鉴别诊断。该病原病毒成功地在 SPF 鸡胚的尿囊膜上分离,表现出痘病毒科的典型痘疱病变。电子显微镜检查显示出负染的椭圆形病毒粒子,这是副痘病毒属成员的特征。从分离物中提取的 DNA 经 PCR 扩增出了羊口疮病毒晚期转录因子(VLTF-1)基因的 392bp 片段。系统进化分析显示,与世界范围内报告的其他羊口疮病毒株具有 99%的同一性。本研究中应用的临床标本的选择和处理以及 PCR 检测方法为羊口疮感染提供了可靠的实验室诊断工具,并首次对埃及羊口疮分离株进行了分子特征分析。