September
2008
, Volume
92
, Number
9
Pages
1,313
-
1,320
Authors
M. Rännäli and
V. Czekaj, Department of Applied Biology, P.O. Box 27, FIN-00014 University of Helsinki, Finland;
R. A. C. Jones, Agricultural Research Western Australia, Locked Bag No. 4, Bentley Delivery Centre, Perth, WA 6983, and WA State Agricultural Biotechnology Centre, Murdoch University, Perth, WA 6150, Australia;
J. D. Fletcher, New Zealand Institute for Crop & Food Research, Private Bag 4704, Christchurch, New Zealand;
R. I. Davis, Northern Australia Quarantine Strategy (NAQS) and Australian Quarantine and Inspection Service (AQIS), P.O. Box 1054, Mareeba, Queensland 4880, Australia;
L. Mu, Service du Dévelopement Rural, Département de la Protection des Végétaux, BP 100, Papeete, French Polynesia;
G. I. Dwyer and
B. A. Coutts, Agricultural Research Western Australia, Locked Bag No. 4, Bentley Delivery Centre, Perth, WA 6983, Australia; and
J. P. T. Valkonen, Department of Applied Biology, P.O. Box 27, FIN-00014 University of Helsinki, Finland
Affiliations
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RelatedArticle
Accepted for publication 16 May 2008.
Abstract
ABSTRACT
Sweet potato virus G (SPVG, genus Potyvirus, family Potyviridae) was detected in sweetpotato (Ipomoea batatas) storage roots sold in the local markets and storage roots or cuttings sampled directly from farmers' fields. Using serological and molecular methods, the virus was detected for the first time in Java, New Zealand, Hawaii, Tahiti, Tubuai, Easter Island, Zimbabwe, and South Africa, and also in an imported storage root under post-entry quarantine conditions in Western Australia. In some specimens, SPVG was detected in mixed infection with Sweet potato feathery mottle virus (genus Potyvirus). The coat protein (CP) encoding sequences of SPVG were analyzed for 11 plants from each of the aforementioned locations and compared with the CP sequences of 12 previously characterized isolates from China, Egypt, Ethiopia, Spain, Peru, and the continental United States. The nucleotide sequence identities of all SPVG isolates ranged from 79 to 100%, and amino acid identities ranged from 89 to 100%. Isolates of the same strain of SPVG had nucleotide and amino acid sequence identities from 97 to 100% and 96 to 100%, respectively, and were found in sweetpotatoes from all countries sampled except Peru. Furthermore, a plant from Zimbabwe was co-infected with two clearly different SPVG isolates of this strain. In contrast, three previously characterized isolates from China and Peru were phylogenetically distinct and exhibited <90% nucleotide identity with any other isolate. So far, the highest genetic diversity of SPVG seems to occur among isolates in China. Distribution of SPVG within many sweetpotato growing areas of the world emphasizes the need to determine the economic importance of SPVG.
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© 2008 The American Phytopathological Society