header
Image from OpenLibrary

Study the changes in pathogenicity of H9N2 avian influenza virus after the use of live attenuated vaccines in broiler chickens / Zainab Mohamed Esmail ; Supervised Hussein Ali Hussein , Ayman H. M. Eldeeb , Mounir Mohamed Elsafty

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Zainab Mohamed Esmail , 2018Description: 117 P. : charts , photographs ; 25cmOther title:
  • بعد استخدام اللقاحات الحيه المستضعفه فى بدارى التسمين (H9N2) دراسه التغييرات فى ضراوه فيروس انفلونزا الطيور [Added title page title]
Subject(s): Available additional physical forms:
  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Virology Summary: Low pathogenic H9N2 avian influenza virus (AIV) causes great economic losses in broiler chickens. In the present study, two experiments were carried out for studying the pathogenicity of H9N2 AIV in broiler chickens after vaccination with different live respiratory viral vaccines. One-day- old specific pathogen free (SPF) chicks were divided into four groups in each experiment. In experiment 1; groups 1 and 2 were inoculated with H9N2 AIV via nasal route at 1st day old, groups 1 and 3 were vaccinated with live IBV vaccine at 5th days old and group 4 was left as a negative control. In experiment 2; groups 5and 6were inoculated with AIV subtype H9N2 via nasal route at 1st day old, group 5 was vaccinated with live IBV vaccine and live NDV vaccine at 5th days and 18th days old; respectively, groups 6 and 7 were vaccinated with live NDV vaccine at 18th days old and group 8 was left as a negative control. Chicks were kept in isolators for 18 days in first experiment and 35 days in the second experiment. Tracheal and Cloacal swabs were collected at 3rd, 5th, 7th, 10th, 12th and 15th days old from all groups in experiment 1; 21th, 23th, 25th and 28th days old from all groups in experiment 2. Quantitative Real time (rRT-PCR) was applied on the collected tracheal swabs for detecting RNA copies of H9N2 AIV and revealed a significant increase in H9N2 AIV titer with extension in the period of viral shedding in groups 1 and 5
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.10.17.M.Sc.2018.Za.S (Browse shelf(Opens below)) Not for loan 01010110077256000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.10.17.M.Sc.2018.Za.S (Browse shelf(Opens below)) 77256.CD Not for loan 01020110077256000

Thesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Virology

Low pathogenic H9N2 avian influenza virus (AIV) causes great economic losses in broiler chickens. In the present study, two experiments were carried out for studying the pathogenicity of H9N2 AIV in broiler chickens after vaccination with different live respiratory viral vaccines. One-day- old specific pathogen free (SPF) chicks were divided into four groups in each experiment. In experiment 1; groups 1 and 2 were inoculated with H9N2 AIV via nasal route at 1st day old, groups 1 and 3 were vaccinated with live IBV vaccine at 5th days old and group 4 was left as a negative control. In experiment 2; groups 5and 6were inoculated with AIV subtype H9N2 via nasal route at 1st day old, group 5 was vaccinated with live IBV vaccine and live NDV vaccine at 5th days and 18th days old; respectively, groups 6 and 7 were vaccinated with live NDV vaccine at 18th days old and group 8 was left as a negative control. Chicks were kept in isolators for 18 days in first experiment and 35 days in the second experiment. Tracheal and Cloacal swabs were collected at 3rd, 5th, 7th, 10th, 12th and 15th days old from all groups in experiment 1; 21th, 23th, 25th and 28th days old from all groups in experiment 2. Quantitative Real time (rRT-PCR) was applied on the collected tracheal swabs for detecting RNA copies of H9N2 AIV and revealed a significant increase in H9N2 AIV titer with extension in the period of viral shedding in groups 1 and 5

Issued also as CD

There are no comments on this title.

to post a comment.