May
2006
, Volume
96
, Number
5
Pages
542
-
548
Authors
Marcel
Maymon
,
Aida
Zveibil
,
Shimon
Pivonia
,
Dror
Minz
,
and
Stanley
Freeman
Affiliations
First, second, and fifth authors: Department of Plant Pathology; and fourth author: Institute of Soil, Water, and Environmental Sciences, ARO, The Volcani Center, Bet Dagan 50250, Israel; and third author: Arava R&D, Sapir, 868252, Israel
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RelatedArticle
Accepted for publication 9 January 2006.
Abstract
ABSTRACT
Sixty-four isolates of Colletotrichum gloeosporioides were isolated from infected Limonium spp. cultivated in 12 different locations in Israel. All isolates were identified as belonging to the C. gloeosporioides complex by species-specific primers. Of these isolates, 46 were resistant to benomyl at 10 μg/ml and 18 were sensitive to this concentration of fungicide. Based on arbitrarily primed polymerase chain reaction of all isolates and internal transcribed spacer-1 sequence analyses of 12 selected isolates, the benomyl-resistant and -sensitive populations belong to two distinct genotypes. Sequence analyses of the β-tubulin genes, TUB1 and TUB2, of five sensitive and five resistant representative isolates of C. gloeosporioides from Limonium spp. revealed that the benomyl-resistant isolates had an alanine substitute instead of a glutamic acid at position 198 in TUB2. All data suggest that the resistant and sensitive genotypes are two independent and separate populations. Because all Limonium plant propagation material is imported from various geographic regions worldwide, and benomyl is not applied to this crop or for the control of Colletotrichum spp. in Israel, it is presumed that plants are bearing quiescent infections from the points of origin prior to arrival.
JnArticleKeywords
Additional keyword:
anthracnose.
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ArticleCopyright
© 2006 The American Phytopathological Society