|
|
||||||||
Animal: RNA Viruses |
Laboratory of Virology and Chemotherapy1 and Laboratory of Clinical and Epidemiological Virology2, Rega Institute for Medical Research, Minderbroedersstraat 10, B-3000 Leuven, Belgium
Leiden Institute of Chemistry, Leiden University, PO Box 9502, 2300 RA Leiden, The Netherlands3
Unité des Virus Emergents, Faculté de Médecine de Marseille, 27 Boulevard Jean Moulin, 13005 Marseille cedex 5, France4
Author for correspondence: Johan Neyts. Fax +32 16 33 73 40. e-mail johan.neyts{at}rega.kuleuven.ac.be
Montana Myotis leukoencephalitis virus (MMLV), a virus isolated from bats, causes an encephalitis in small rodents reminiscent of flavivirus encephalitis in humans. The complete MMLV genome is 10690 nucleotides long and encodes a putative polyprotein of 3374 amino acids. The virus contains the same conserved motifs in genes that are believed to be interesting antiviral targets (NTPase/helicase, serine protease and RNA-dependent RNA polymerase) as flaviviruses of clinical importance. Phylogenetic analysis of the entire coding region has confirmed the classification of MMLV in the clade of the flaviviruses with no known vector (NKV) and within this clade to the Rio Bravo branch (both viruses have the bat as their vertebrate host). We have provided for the first time a comparative analysis of the RNA folding of the 3' UTR of the NKV flaviviruses (Modoc, Rio Bravo and Apoi viruses, in addition to MMLV). Structural elements in the 3' UTR that are preserved among other flaviviruses have been revealed, as well as elements that distinguish the NKV from the mosquito- and tick-borne flaviviruses. In particular, the pentanucleotide sequence 5' CACAG 3', which is conserved in all mosquito- and tick-borne flaviviruses, is replaced by the sequence 5' C(C/U)(C/U)AG 3' in the loop of the 3' long stable hairpin structure of all four NKV flaviviruses. The availability of this latter sequence motif allows us to designate a virus as either an NKV or a vector-borne flavivirus.
This article has been cited by other articles:
![]() |
P. A. G. C. Silva, R. Molenkamp, T. J. Dalebout, N. Charlier, J. H. Neyts, W. J. M. Spaan, and P. J. Bredenbeek Conservation of the pentanucleotide motif at the top of the yellow fever virus 17D 3' stem-loop structure is not required for replication J. Gen. Virol., June 1, 2007; 88(6): 1738 - 1747. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. S. Gritsun and E. A. Gould Direct repeats in the 3' untranslated regions of mosquito-borne flaviviruses: possible implications for virus transmission. J. Gen. Virol., November 1, 2006; 87(Pt 11): 3297 - 3305. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. S. Gritsun and E. A. Gould The 3' untranslated regions of Kamiti River virus and Cell fusing agent virus originated by self-duplication J. Gen. Virol., September 1, 2006; 87(9): 2615 - 2619. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. DAVIS, M. BUNNING, P. GORDY, N. PANELLA, B. BLITVICH, and R. BOWEN EXPERIMENTAL AND NATURAL INFECTION OF NORTH AMERICAN BATS WITH WEST NILE VIRUS Am J Trop Med Hyg, August 1, 2005; 73(2): 467 - 469. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Bryant, P. F. C. Vasconcelos, R. C. A. Rijnbrand, J. P. Mutebi, S. Higgs, and A. D. T. Barrett Size Heterogeneity in the 3' Noncoding Region of South American Isolates of Yellow Fever Virus J. Virol., March 15, 2005; 79(6): 3807 - 3821. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Charlier, P. Leyssen, J. Paeshuyse, C. Drosten, H. Schmitz, A. Van Lommel, E. De Clercq, and J. Neyts Infection of SCID mice with Montana Myotis leukoencephalitis virus as a model for flavivirus encephalitis J. Gen. Virol., August 1, 2002; 83(8): 1887 - 1896. [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 | |