Synonymous site variation due to recombination explains higher genetic variability in begomovirus populations infecting non-cultivated hosts
| dc.contributor.author | Lima, Alison T. M. | |
| dc.contributor.author | Sobrinho, Roberto R. | |
| dc.contributor.author | González-Aguilera, Jorge | |
| dc.contributor.author | Rocha, Carolina S. | |
| dc.contributor.author | Silva, Sarah J. C. | |
| dc.contributor.author | Xavier, César A. D. | |
| dc.contributor.author | Silva, Fábio N. | |
| dc.contributor.author | Zerbini, F. Murilo | |
| dc.contributor.author | Duffy, Siobain | |
| dc.date.accessioned | 2017-11-14T13:49:53Z | |
| dc.date.available | 2017-11-14T13:49:53Z | |
| dc.date.issued | 2013-02-01 | |
| dc.description.abstract | Begomoviruses are ssDNA plant viruses that cause serious epidemics in economically important crops worldwide. Non-cultivated plants also harbour many begomoviruses, and it is believed that these hosts may act as reservoirs and as mixing vessels where recombination may occur. Begomoviruses are notoriously recombination-prone, and also display nucleotide substitution rates equivalent to those of RNA viruses. In Brazil, several indigenous begomoviruses have been described infecting tomatoes following the introduction of a novel biotype of the whitefly vector in the mid-1990s. More recently, a number of viruses from non-cultivated hosts have also been described. Previous work has suggested that viruses infecting non-cultivated hosts have a higher degree of genetic variability compared with crop-infecting viruses. We intensively sampled cultivated and non-cultivated plants in similarly sized geographical areas known to harbour either the weed-infecting Macroptilium yellow spot virus (MaYSV) or the crop-infecting Tomato severe rugose virus (ToSRV), and compared the molecular evolution and population genetics of these two distantly related begomoviruses. The results reinforce the assertion that infection of non-cultivated plant species leads to higher levels of standing genetic variability, and indicate that recombination, not adaptive selection, explains the higher begomovirus variability in non-cultivated hosts. | en |
| dc.format | pt-BR | |
| dc.identifier.issn | 1465-2099 | |
| dc.identifier.uri | http://dx.doi.org/10.1099/vir.0.047241-0 | |
| dc.identifier.uri | http://www.locus.ufv.br/handle/123456789/13066 | |
| dc.language.iso | eng | pt-BR |
| dc.publisher | Journal of General Virology | pt-BR |
| dc.relation.ispartofseries | Volume 94, Issue 2, p. 418-431, February 2013 | pt-BR |
| dc.rights | Open Access | pt-BR |
| dc.subject | Synonymous site variation | pt-BR |
| dc.subject | Recombination | pt-BR |
| dc.subject | Genetic variability | pt-BR |
| dc.subject | Begomovirus | pt-BR |
| dc.title | Synonymous site variation due to recombination explains higher genetic variability in begomovirus populations infecting non-cultivated hosts | en |
| dc.type | Artigo | pt-BR |
