|
|
||||||||
AFRC Institute for Animal Health, Compton Laboratory, Near Newbury, Berkshire RG16 0NN, U.K.
Part of genomic segment A of five recent European very virulent (VV) isolates of infectious bursal disease virus, encoding the major, conformational, protective epitope, have been reverse-transcribed, amplified and cloned. Sequence analysis of 582 bases of VP2 showed that the four U.K. isolates are closely related to each other, differing by no more than two bases, but are distinct from the classical type 1 strains (differing by at least 29 bases, or four amino acids, from any other strain and by 15 bases, or three amino acids, from the consensus sequence of all other strains). The U.K. isolates differ from an earlier VV isolate from the Netherlands by no more than five bases or two amino acids. The U.K. isolates differ by only one or two bases, with no amino acid changes, from the recently published sequence of a Japanese VV isolate.
Received 16 August 1993;
accepted 11 October 1993.
This article has been cited by other articles:
![]() |
F. Le Goff, I. Mederle-Mangeot, A. Jestin, and P. Langlois Deletion of open reading frames 9, 10 and 11 from the avian adenovirus CELO genome: effect on biodistribution and humoral responses J. Gen. Virol., July 1, 2005; 86(7): 2019 - 2027. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Brandt, K. Yao, M. Liu, R. A. Heckert, and V. N. Vakharia Molecular Determinants of Virulence, Cell Tropism, and Pathogenic Phenotype of Infectious Bursal Disease Virus J. Virol., December 15, 2001; 75(24): 11974 - 11982. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Mundt Tissue culture infectivity of different strains of infectious bursal disease virus is determined by distinct amino acids in VP2 J. Gen. Virol., August 1, 1999; 80(8): 2067 - 2076. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |