J Gen Virol Try Microbiology Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 84 (2003), 2691-2703; DOI 10.1099/vir.0.19277-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chare, E. R.
Right arrow Articles by Holmes, E. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chare, E. R.
Right arrow Articles by Holmes, E. C.
Agricola
Right arrow Articles by Chare, E. R.
Right arrow Articles by Holmes, E. C.
© 2003 Society for General Microbiology

Phylogenetic analysis reveals a low rate of homologous recombination in negative-sense RNA viruses

Elizabeth R. Chare1, Ernest A. Gould2 and Edward C. Holmes1

1 Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK
2 Centre for Ecology and Hydrology, Mansfield Road, Oxford, UK

Correspondence
Edward Holmes
Edward.Holmes{at}zoo.ox.ac.uk

Recombination is increasingly seen as an important means of shaping genetic diversity in RNA viruses. However, observed recombination frequencies vary widely among those viruses studied to date, with only sporadic occurrences reported in RNA viruses with negative-sense genomes. To determine the extent of homologous recombination in negative-sense RNA viruses, phylogenetic analyses of 79 gene sequence alignments from 35 negative-sense RNA viruses (a total of 2154 sequences) were carried out. Powerful evidence was found for recombination, in the form of incongruent phylogenetic trees between different gene regions, in only five sequences from Hantaan virus, Mumps virus and Newcastle disease virus. This is the first report of recombination in these viruses. More tentative evidence for recombination, where conflicting phylogenetic trees were observed (but were without strong bootstrap support) and/or where putative recombinant regions were very short, was found in three alignments from La Crosse virus and Puumala virus. Finally, patterns of sequence variation compatible with the action of recombination, but not definitive evidence for this process, were observed in a further ten viruses: Canine distemper virus, Crimean-Congo haemorrhagic fever virus, Influenza A virus, Influenza B virus, Influenza C virus, Lassa virus, Pirital virus, Rabies virus, Rift Valley Fever virus and Vesicular stomatitis virus. The possibility of recombination in these viruses should be investigated further. Overall, this study reveals that rates of homologous recombination in negative-sense RNA viruses are very much lower than those of mutation, with many viruses seemingly clonal on current data. Consequently, recombination rate is unlikely to be a trait that is set by natural selection to create advantageous or purge deleterious mutations.




This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
M. Razzauti, A. Plyusnina, H. Henttonen, and A. Plyusnin
Accumulation of point mutations and reassortment of genomic RNA segments are involved in the microevolution of Puumala hantavirus in a bank vole (Myodes glareolus) population
J. Gen. Virol., July 1, 2008; 89(7): 1649 - 1660.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
F. M. Codoner and S. F. Elena
The promiscuous evolutionary history of the family Bromoviridae
J. Gen. Virol., July 1, 2008; 89(7): 1739 - 1747.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
G.-Z. Han, X.-P. Liu, and S.-S. Li
Caution about Newcastle Disease Virus-Based Live Attenuated Vaccine
J. Virol., July 1, 2008; 82(13): 6782 - 6782.
[Full Text] [PDF]


Home page
J. Virol.Home page
M. F. Boni, Y. Zhou, J. K. Taubenberger, and E. C. Holmes
Homologous Recombination Is Very Rare or Absent in Human Influenza A Virus
J. Virol., May 15, 2008; 82(10): 4807 - 4811.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
T. J. Wittmann, R. Biek, A. Hassanin, P. Rouquet, P. Reed, P. Yaba, X. Pourrut, L. A. Real, J.-P. Gonzalez, and E. M. Leroy
Isolates of Zaire ebolavirus from wild apes reveal genetic lineage and recombinants
PNAS, October 23, 2007; 104(43): 17123 - 17127.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
R. Belshaw, O. G. Pybus, and A. Rambaut
The evolution of genome compression and genomic novelty in RNA viruses
Genome Res., October 1, 2007; 17(10): 1496 - 1504.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
C. A. Macken, R. J. Webby, and W. J. Bruno
Genotype turnover by reassortment of replication complex genes from avian Influenza A virus.
J. Gen. Virol., October 1, 2006; 87(Pt 10): 2803 - 2815.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
S. L. Kosakovsky Pond, D. Posada, M. B. Gravenor, C. H. Woelk, and S. D. W. Frost
Automated Phylogenetic Detection of Recombination Using a Genetic Algorithm
Mol. Biol. Evol., October 1, 2006; 23(10): 1891 - 1901.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
V. M. Deyde, M. L. Khristova, P. E. Rollin, T. G. Ksiazek, and S. T. Nichol
Crimean-congo hemorrhagic Fever virus genomics and global diversity.
J. Virol., September 1, 2006; 80(17): 8834 - 8842.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
G. J. Etherington, S. M. Ring, M. A. Charleston, J. Dicks, V. J. Rayward-Smith, and I. N. Roberts
Tracing the origin and co-phylogeny of the caliciviruses.
J. Gen. Virol., May 1, 2006; 87(Pt 5): 1229 - 1235.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
J. Chamberlain, N. Cook, G. Lloyd, V. Mioulet, H. Tolley, and R. Hewson
Co-evolutionary patterns of variation in small and large RNA segments of Crimean-Congo hemorrhagic fever virus
J. Gen. Virol., December 1, 2005; 86(12): 3337 - 3341.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
P. L. Davis, E. C. Holmes, F. Larrous, W. H. M. Van der Poel, K. Tjornehoj, W. J. Alonso, and H. Bourhy
Phylogeography, Population Dynamics, and Molecular Evolution of European Bat Lyssaviruses
J. Virol., August 15, 2005; 79(16): 10487 - 10497.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
A. N. Lukashev
Evidence for recombination in Crimean-Congo hemorrhagic fever virus
J. Gen. Virol., August 1, 2005; 86(8): 2333 - 2338.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. Furio, A. Moya, and R. Sanjuan
The cost of replication fidelity in an RNA virus
PNAS, July 19, 2005; 102(29): 10233 - 10237.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
J. Rohayem, J. Munch, and A. Rethwilm
Evidence of Recombination in the Norovirus Capsid Gene
J. Virol., April 15, 2005; 79(8): 4977 - 4990.
[Abstract] [Full Text] [PDF]


Home page
RNAHome page
S. O. GUDIMA, J. CHANG, and J. M. TAYLOR
Reconstitution in cultured cells of replicating HDV RNA from pairs of less than full-length RNAs
RNA, January 1, 2005; 11(1): 90 - 98.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
A. V. Ivshina, G. M. Vodeiko, V. A. Kuznetsov, D. Volokhov, R. Taffs, V. I. Chizhikov, R. A. Levandowski, and K. M. Chumakov
Mapping of Genomic Segments of Influenza B Virus Strains by an Oligonucleotide Microarray Method
J. Clin. Microbiol., December 1, 2004; 42(12): 5793 - 5801.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
I. S. Novella, D. D. Reissig, and C. O. Wilke
Density-Dependent Selection in Vesicular Stomatitis Virus
J. Virol., June 1, 2004; 78(11): 5799 - 5804.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
Z. Huang, A. Panda, S. Elankumaran, D. Govindarajan, D. D. Rockemann, and S. K. Samal
The Hemagglutinin-Neuraminidase Protein of Newcastle Disease Virus Determines Tropism and Virulence
J. Virol., April 15, 2004; 78(8): 4176 - 4184.
[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
Copyright © 2003 by the Society for General Microbiology.