ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE

In the present study, Vero cell line was tested for its ability to support the replication of indigenous very virulent infectious bursal disease virus (vvIBDV). The frozen cells were resuscitated to prepare monolayer, which was further sub-cultured to prepare semi-confluent monolayers using M199 gro...

Full description

Bibliographic Details
Main Author: I. Hussain and M. H. Rasool
Format: Article
Language:English
Published: University of Agriculture, Faisalabad 2005-07-01
Series:Pakistan Veterinary Journal
Subjects:
Online Access:http://www.pvj.com.pk/pdf-files/25_3/103-106.pdf
id doaj-ccb17d1fd160412096600a75bda26191
record_format Article
spelling doaj-ccb17d1fd160412096600a75bda261912020-11-24T22:06:28ZengUniversity of Agriculture, FaisalabadPakistan Veterinary Journal0253-83182005-07-01253103106ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINEI. Hussain and M. H. RasoolIn the present study, Vero cell line was tested for its ability to support the replication of indigenous very virulent infectious bursal disease virus (vvIBDV). The frozen cells were resuscitated to prepare monolayer, which was further sub-cultured to prepare semi-confluent monolayers using M199 growth medium supplemented with 5% foetal calf serum. The semi confluent monolayers were then infected with 0.25 ml of indigenous vvIBDV. The passage 1 virus was harvested and used for the next passage. In this way virus was given three serial passages on Vero cell line, where characteristic cytopathic effects (CPEs) were observed. During the first passage, no CPEs were found. The Vero cell monolayers remained normal in first passage upto 144 hours post-infection. During second passage, rounding of cells was observed after 72 hours of infection. However, clear and consistent CPEs were not observed in 2nd passage. Typical aggregation, rounding and granulation of Vero cells was noticed in passage 3 (P3) from 72 hours upto 144 hours post-infection. The positive results of agar gel precipitation test (AGPT) confirmed that the adapted (P3) virus was IBDV. The infectivity titer of adapted vvIBDV was found to be log10 7.60 TCID50/ ml at 72 hours post-infection. The indigenous vvIBDV was well adapted to Vero cell line after three successive passages.http://www.pvj.com.pk/pdf-files/25_3/103-106.pdfVery virulentInfectious bursal disease virusVero cell linecytopathic effects
collection DOAJ
language English
format Article
sources DOAJ
author I. Hussain and M. H. Rasool
spellingShingle I. Hussain and M. H. Rasool
ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
Pakistan Veterinary Journal
Very virulent
Infectious bursal disease virus
Vero cell line
cytopathic effects
author_facet I. Hussain and M. H. Rasool
author_sort I. Hussain and M. H. Rasool
title ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
title_short ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
title_full ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
title_fullStr ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
title_full_unstemmed ADAPTATION OF AN INDIGENOUS VERY VIRULENT INFECTIOUS BURSAL DISEASE VIRUS ON VERO CELL LINE
title_sort adaptation of an indigenous very virulent infectious bursal disease virus on vero cell line
publisher University of Agriculture, Faisalabad
series Pakistan Veterinary Journal
issn 0253-8318
publishDate 2005-07-01
description In the present study, Vero cell line was tested for its ability to support the replication of indigenous very virulent infectious bursal disease virus (vvIBDV). The frozen cells were resuscitated to prepare monolayer, which was further sub-cultured to prepare semi-confluent monolayers using M199 growth medium supplemented with 5% foetal calf serum. The semi confluent monolayers were then infected with 0.25 ml of indigenous vvIBDV. The passage 1 virus was harvested and used for the next passage. In this way virus was given three serial passages on Vero cell line, where characteristic cytopathic effects (CPEs) were observed. During the first passage, no CPEs were found. The Vero cell monolayers remained normal in first passage upto 144 hours post-infection. During second passage, rounding of cells was observed after 72 hours of infection. However, clear and consistent CPEs were not observed in 2nd passage. Typical aggregation, rounding and granulation of Vero cells was noticed in passage 3 (P3) from 72 hours upto 144 hours post-infection. The positive results of agar gel precipitation test (AGPT) confirmed that the adapted (P3) virus was IBDV. The infectivity titer of adapted vvIBDV was found to be log10 7.60 TCID50/ ml at 72 hours post-infection. The indigenous vvIBDV was well adapted to Vero cell line after three successive passages.
topic Very virulent
Infectious bursal disease virus
Vero cell line
cytopathic effects
url http://www.pvj.com.pk/pdf-files/25_3/103-106.pdf
work_keys_str_mv AT ihussainandmhrasool adaptationofanindigenousveryvirulentinfectiousbursaldiseasevirusonverocellline
_version_ 1725823562179149824