June
2002
, Volume
86
, Number
6
Pages
682
-
686
Authors
Karsten
Nielsen
,
Department of Crop Protection, Danish Institute of Agricultural Sciences, Research Center Flakkebjerg, 4200 Slagelse, Denmark
;
David S.
Yohalem
,
Department of Crop Protection, Danish Institute of Agricultural Sciences, Research Center Flakkebjerg, 4200 Slagelse, Denmark
;
Dan Funck
Jensen
,
Department of Plant Biology, The Royal Veterinary and Agricultural University, 1841 Frederiksberg, Denmark
Affiliations
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RelatedArticle
Accepted for publication 14 February 2002.
Abstract
ABSTRACT
Botrytis aclada and other Botrytis spp. can cause neck rot on onions, a storage disease that normally is very difficult to detect at harvest using traditional isolation techniques. Sequence characterized amplified region primers (BA2f/BA1r) were designed based on a previously cloned and amplified DNA fragment for direct amplification of isolates of Botrytis spp. associated with neck rot of onions. Digestion of the polymerase chain reaction (PCR) amplification product with the restriction enzyme ApoI makes it possible to distinguish the five groups: Botrytis aclada types AI and AII (B. allii); B. byssoidea; B. squamosa; and B. cinerea. The detection limit was 1 to 10 pg of pure fungal DNA. It was possible to detect B. aclada with the PCR method in artificially inoculated onion bulb tissue and in mature onion leaves showing no symptoms of the disease. The availability of a sensitive and specific PCR detection and identification method for Botrytis onion neck rot pathogens should facilitate ecological studies of this group of onion pathogens.
JnArticleKeywords
Additional keywords:
Allium,
Botryotinia,
SCAR,
UP-PCR
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ArticleCopyright
© 2002 The American Phytopathological Society