July
1997
, Volume
87
, Number
7
Pages
745
-
750
Authors
Nichole R.
O'Neill
,
Peter
van Berkum
,
Jhy-Jhu
Lin
,
Jonathan
Kuo
,
George N.
Ude
,
William
Kenworthy
,
and
James A.
Saunders
Affiliations
First, second, and seventh authors: USDA, ARS, Beltsville, MD 20705; third and fourth authors: Life Technologies, Inc., 8717 Grovemont Circle, Gaithersburg, MD; fifth and sixth authors: Department of Agronomy, University of Maryland, College Park 20742
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RelatedArticle
Accepted for publication 8 April 1997.
Abstract
ABSTRACT
Amplified restriction fragment length polymorphism (AFLP) was used to assess the levels of genomic variations among species and isolates of the genus Colletotrichum. Our objective was to characterize at the molecular level two alfalfa pathogens, isolates Arl-NW and 57RR, which are unusually aggressive to anthracnose-resistant alfalfa cultivars and whose taxa has been uncertain based on morphological criteria. The fingerprint patterns obtained were complex but did enable us to place these two isolates within the species C. trifolii and C. gloeosporioides, respectively. The diversity detected with AFLP among and within Colletotrichum species from alfalfa and other crops corroborated their published taxonomy based on morphology, ribosomal DNA sequence, and random amplified polymorphic DNA analyses. Similarity matrices generated with three primer pairs were highly correlated and, thus, were combined to determine the similarity among the fungal species and isolates that were analyzed. Analysis of the data generated with each of the primer pairs individually and application of either distance or parsimony methods supported the placement of these two isolates. The parsimony method of data analysis was more confirmatory in the placement of Phoma medicaginis as an out-group than the distance method, using either simple matching or Jaccard's coefficients to generate the similarity matrices. Our conclusion is that the AFLP technique will be useful for identification of individual isolates within complex genera such as Colletotrichum because of its ability to generate large numbers of polymorphisms and the consistency of polymerase chain reaction amplification.
JnArticleKeywords
Additional keywords:
DNA fingerprinting,
Medicago sativa,
PCR.
Page Content
ArticleCopyright
The American Phytopathological Society, 1997