February
2002
, Volume
86
, Number
2
Pages
106
-
111
Authors
R. R.
Walcott
,
Department of Plant Pathology, University of Georgia, Athens 30602
;
R. D.
Gitaitis
,
Department of Plant Pathology, University of Georgia, Coastal Plain Experiment Station Tifton 31793
;
A. C.
Castro
,
Department of Plant Pathology, University of Georgia, Athens 30602
;
F. H.
Sanders
Jr.
,
Department of Plant Pathology, University of Georgia, Coastal Plain Experiment Station Tifton 31793
; and
J. C.
Diaz-Perez
,
Department of Horticulture, University of Georgia, Coastal Plain Experiment Station, Tifton 31793
Affiliations
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RelatedArticle
Accepted for publication 8 October 2001.
Abstract
ABSTRACT
An immunomagnetic separation and polymerase chain reaction (IMS-PCR) assay was used to detect Pantoea ananatis in naturally infested onion seeds. Using species-specific PCR primers and polyclonal antibodies, IMS-PCR consistently demonstrated detection thresholds of 101 to 103 CFU/ml. There was no significant difference between the numbers of CFU recovered from onion seed wash by IMS (after repeated rinses) and by direct plating, indicating that IMS effectively captured P. ananatis cells from heterogeneous bacterial populations. Using IMS-PCR and IMS followed by plating on nutrient agar, P. ananatis was detected in 19.7% of onion seed samples harvested from two onion fields in which center rot developed naturally in 2000. When planted in germination boxes, 53% of the seed samples that tested positive for P. ananatis produced seedlings with symptoms of center rot. There was no significant difference in germination between infested and noninfested seed samples. This is the first report of natural infestation and transmission of P. ananatis in onion seed.
JnArticleKeywords
Additional keywords:
Erwinia ananas,
E. herbicola
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ArticleCopyright
© 2002 The American Phytopathological Society