|
|
||||||||
1 Department of Entomology, Penn State University, University Park, PA 16803, USA
2 National Microbiology Laboratory, Health Canada, Winnipeg, Manitoba, Canada R3E 3R2
3 Department of Biochemistry, Penn State University, University Park, PA 16803, USA
4 Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada B3H 4R2
Correspondence
J. R. de Miranda
joachimdemiranda{at}yahoo.com
The complete nucleotide sequence of a novel virus is presented here together with serological evidence that it belongs to Kashmir bee virus (KBV). Analysis reveals that KBV is a cricket paralysis-like virus (family Dicistroviridae: genus Cripavirus), with a non-structural polyprotein open reading frame in the 5' portion of the genome separated by an intergenic region from a structural polyprotein open reading frame in the 3' part of the genome. The genome also has a polyadenylated tail at the 3' terminus. KBV is one of several related viruses that also includes acute bee paralysis virus (ABPV). Although KBV and ABPV are about 70 % identical over the entire genome, there are considerable differences between them in significant areas of the genome, such as the 5' non-translated region (42 % nucleotide identity), between the helicase and 3C-protease domains of the non-structural polyprotein (57 % amino acid identity) and in a 90 aa stretch of the structural polyprotein (33 % amino acid identity). Phylogenetic analyses show that KBV and ABPV isolates fall into clearly separated clades with moderate evolutionary distance between them. Whether these genomic and evolutionary differences are sufficient to classify KBV and ABPV as separate species remains to be determined.
The GenBank accession numbers for the nucleotide sequences reported in this paper are AY452696 and AY275710.
This article has been cited by other articles:
![]() |
G. A. Luke, P. de Felipe, A. Lukashev, S. E. Kallioinen, E. A. Bruno, and M. D. Ryan Occurrence, function and evolutionary origins of '2A-like' sequences in virus genomes J. Gen. Virol., April 1, 2008; 89(4): 1036 - 1042. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Maori, S. Lavi, R. Mozes-Koch, Y. Gantman, Y. Peretz, O. Edelbaum, E. Tanne, and I. Sela Isolation and characterization of Israeli acute paralysis virus, a dicistrovirus affecting honeybees in Israel: evidence for diversity due to intra- and inter-species recombination J. Gen. Virol., December 1, 2007; 88(12): 3428 - 3438. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Berenyi, T. Bakonyi, I. Derakhshifar, H. Koglberger, G. Topolska, W. Ritter, H. Pechhacker, and N. Nowotny Phylogenetic Analysis of Deformed Wing Virus Genotypes from Diverse Geographic Origins Indicates Recent Global Distribution of the Virus Appl. Envir. Microbiol., June 1, 2007; 73(11): 3605 - 3611. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Lanzi, J. R. de Miranda, M. B. Boniotti, C. E. Cameron, A. Lavazza, L. Capucci, S. M. Camazine, and C. Rossi Molecular and Biological Characterization of Deformed Wing Virus of Honeybees (Apis mellifera L.). J. Virol., May 1, 2006; 80(10): 4998 - 5009. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Berenyi, T. Bakonyi, I. Derakhshifar, H. Koglberger, and N. Nowotny Occurrence of Six Honeybee Viruses in Diseased Austrian Apiaries Appl. Envir. Microbiol., April 1, 2006; 72(4): 2414 - 2420. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Shen, L. Cui, N. Ostiguy, and D. Cox-Foster Intricate transmission routes and interactions between picorna-like viruses (Kashmir bee virus and sacbrood virus) with the honeybee host and the parasitic varroa mite J. Gen. Virol., August 1, 2005; 86(8): 2281 - 2289. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |