作者: ZA Al-Khafaji , Ghanim Aboud Al-Mola , A Youins , K Al-Khafaji
DOI:
关键词: Viral shedding 、 Viral load 、 Virology 、 Biology 、 Genotyping 、 Nidovirales 、 Genotype 、 Virus 、 Sample collection 、 Torovirus
摘要: Toroviruses are enteric viruses belonging to the Nidovirales order that infect different animal species and human . Torovirus-like particales (TVLPs) immunologically related BRV have been reported as etiological agents of gastroenteritis in humans. The lack “in vitro” culture systems for toroviruses, except prototype Berne virus or BEV, isolated originally from an infected horse, has hampered their study development diagnostic assays. This study describes a real time RT-PCR method detect human torovirus- like particles RNA clinical stool samples using primers corresponding gene coding for nucleocapsid protein which conserved all strains known date. During this study, CT value measured during real-time PCR analysis was used indication viral load found sample assay evaluated with 72 stool children attending Babylon maternity hospital. Fifty tow out (72.2%) were shedding at collection, indicating high incidence TVLPs infection Province. is first attempted for estimating presence Iraq. described provides rapid, highly sensitive, specific reliable detection quantization enabling future epidemiological studies. In addition that included assays group F Adenovirus 250 pediatric subjects exhibiting symptoms diarrhea and/ vomiting which examined. results 10 positive diarrheic confirmed by electron microscopy examination gave clear appearance Till now there no successful virus growth isolation diarrhegenic type 40 41 grow routine cell result reverse transcription – PCR reflected .2 % 58 torovirus adenovirus respectively. genotyping adenoviruses(genotype 41) highlight significance rapid molecular methods screening laboratories provide efficient Keywords : Human Torovirus, Adenovirus, RT-PCR, Electron Microscopy.