Molecular epidemiological investigation of animal hepaciviruses in Egypt / Ayah Muhammed M.M. Hasan ; Supervised Ausama A. A. Yousif Attia , Mohamed Galal Aggour
Material type:
- استقصاء وبائي جزيئي عن فيروسات جنس الهيباسي في الحيوانات في مصر [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.10.17.M.Sc.2018.Ay.M (Browse shelf(Opens below)) | Not for loan | 01010110075945000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.10.17.M.Sc.2018.Ay.M (Browse shelf(Opens below)) | 75945.CD | Not for loan | 01020110075945000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Virology
Equine hepacivirus (EqHV) is one of the non-primate hepaciviruses recently discovered in the Americas, Europe and Asia. It is a hepatotropic member of the genus hepacivirus of Flaviviridae. They are close relatives of hepatitis C virus (HCV). Information on EqHV epidemiology, pathogenesis and genetic diversity is limited. Information regarding prevalence and distribution of NPHV in Egyptian equids does not exist. NS3-specific RT-PCR was used to investigate whether EqHV RNA was present in 436 archival equid serum samples collected from five Egyptian governorates.Of the tested samples, 323 were from Arabian horses (Equus caballus), 28 were from draft horses and, 85 were from donkeys (Equus asinus). EqHV sequences were detected in 10 horses and 2 donkey samples (2.75%). Detection rates were 7.01% (4/57) and 2.11% (8/379) in samples collected during 2015 and 2017, respectively. Phylogenetic analysis based on partial NS3 sequences placed the detected EqHV sequences into two different lineages.Taken together, the data suggests that the circulating viruses may have been introduced during two separate events. During the investigation, a novel pan-hepacivirus-specific RT-PCR assay was developed. The detection sensitivity of the assay resembled that of the reference NS3-specific assay. However, sequencing was not possible using the developed primer set. The novel RT-PCR assay can be used to investigate the presence of previously unidentified hapciviruses using hepatitis C virus as a positive control
Issued also as CD
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