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008 170911s2016 ua dh f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aPh.D
099 _aCai01.10.03.Ph.D.2016.Ah.M
100 0 _aAhlam Abdelhalim Moustafa Mourad
245 1 0 _aMolecular epidemiological studies on the current status of avian influenza virus (H5N1) in poultry in Egypt /
_cAhlam Abdelhalim Moustafa Mourad ; Supervised Diaa Eldein Gad Ahmed Khelfa , Samir Abdelmoez Abdelwanees , Khaled Madian Diab
246 1 5 _aدراسات وبائية جزيئية عن الوضع الحالى لفيروس أنفلونزا الطيور في مصر
260 _aCairo :
_bAhlam Abdelhalim Moustafa Mourad ,
_c2016
300 _a236 P. :
_bcharts , facsimiles ;
_c25cm
502 _aThesis (Ph.D.) - Cairo University - Faculty of Veterinary Medicine - Department of Animal Diseases
520 _aThis study has been pursued to better understand the epidemiological and genetic characters of HPAI viruses in the Egyptian commercial poultry flocks during the period beginning at Dec 2014 to May 2015 and to molecularly identify the predominant Highly pathogenic avian influenza( HPAI H5N1) strain(s) via field investigation for monitoring of different outbreaks of suspected AI infection in different poultry farms, the mortality rate ranged from 50 to 100 %,39 out of 52 samples were positive for HPAI H5N1 (75%) with 9 highly positive samples with Cq ranged from 8.40 to 13.89, The same 39 samples caused deaths of the embryos within 18-36 hr , post inoculation (PI) with positive rapid HA test. The phylogentic analysis revealed that the 9 HPAI H5N1 strains formed a new distinct monophyletic group within 2.2.1.2 clade. One strain out of 39 positive HPAI H5N1 cases, was free from other respiratory viral infection specially H9N2, NDV and IBV, it was titrated using SPF ECE and its titer was 10⁸/ml EID₅₀. Then the pathogenic effect of the predominant HPAI H5N1 A/duck/Egypt/CLEVB-24_N00238/2015 was tested in SPF chickens and the course of the disease was rapid and very severe as the mortality begin at the 2nd DPI and reached to 100% at the 3rd DPI. The clinical signs , post mortem lesions, histopathological examination was recorded, as well as the virus was detected in all freshly dead chickens by real time RT-PCR using specific H5gene primer. The efficacy of 5 commercially available inactivated AI (H5N1, H5N2 and H5N3) vaccines were evaluated against challenging with the current our recently isolated HPAI H5N1 (A/duck/Egypt/CLEVB-24_N00238/2015) field strain using both SPF and broiler chickens
530 _aIssued also as CD
653 4 _aAvian influenza virus (AIV)
653 4 _aH5N1
653 4 _aHighly Pathogenic Avian Influenza (HPAI)
700 0 _aDiaa Eldein Gad Ahmed Khelfa ,
_eSupervisor
700 0 _aKhaled Madian Diab ,
_eSupervisor
700 0 _aSamir Abdelmoez Abdelwanees ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aEnas
_eCataloger
905 _aNazla
_eRevisor
942 _2ddc
_cTH
999 _c62265
_d62265