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Laboratory of Plant Virology, Faculty of Agriculture, Saga University, Saga 840-8502, Japan1
Laboratory of Plant Pathology, Faculty of Agriculture & Life Sciences, Hirosaki University, Hirosaki 036-8561, Japan2
Tohoku Seed Co. Ltd, Utsunomiya 321-3232, Japan3
Plant Pathology & Microbiology Department, Horticulture Research International, Wellesbourne, Warwick CV35 9EF, UK4
Crop & Food Research, Private Bag 4704, Christchurch, New Zealand5
Faculty of Life Science, Zhenjiang University, Hangzhou 310029, PR China6
Department of Virology, Agriculture Research Organization, The Volcani Centre, Bet Dagan 50250, Israel7
Faculty of Science, Australian National University, Canberra, ACT 2601, Australia8
Author for correspondence: Kazusato Ohshima. Fax +81 952 28 8709. e-mail ohshimak{at}cc.saga-u.ac.jp
Turnip mosaic virus (TuMV), a species of the genus Potyvirus, occurs worldwide. Seventy-six isolates of TuMV were collected from around the world, mostly from Brassica and Raphanus crops, but also from several non-brassica species. Host tests grouped the isolates into one or other of two pathotypes; Brassica (B) and BrassicaRaphanus (BR). The nucleotide sequences of the first protein (P1) and coat protein (CP) genes of the isolates were determined. One-tenth of the isolates were found to have anomalous and variable phylogenetic relationships as a result of recombination. The 5'-terminal 300 nt of the P1 gene of many isolates was also variable and phylogenetically anomalous, whereas the 380 nt 3' terminus of the CP gene was mostly conserved. Trees calculated from the remaining informative parts of the two genes of the non-recombinant sequences by neighbour-joining, maximum-likelihood and maximum-parsimony methods were closely similar, and so these parts of the sequences were concatenated and trees calculated from the resulting 1150 nt. The isolates fell into four consistent groups; only the relationships of these groups with one another and with the outgroup differed. The basal-B cluster of eight B-pathotype isolates was most variable, was not monophyletic, and came from both brassicas and non-brassicas from southwest and central Eurasia. Closest to it, and forming a monophyletic subgroup of it in most trees, and similarly variable, was the basal-BR group of eight BR pathotype Eurasian isolates. The third and least variable group, the Asian-BR group, was of 22 BR-pathotype isolates, all from brassicas, mostly Raphanus, and all from east Asia mostly Japan. The fourth group of 36 isolates, the world-B group, was from all continents, most were isolated from brassicas and most were of the B-pathotype. The simplest of several possible interpretations of the trees is that TuMV originated, like its brassica hosts, in Europe and spread to the other parts of the world, and that the BR pathotype has recently evolved in east Asia.
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