Affiliation:
1. Department of Ecology and Evolutionary Biology, University of Toronto, 3359 Mississauga Road North, Mississauga, Ontario L5L 1C6, Canada
Abstract
ABSTRACT
A molecular diagnostic system using single nucleotide polymorphisms (SNPs) was developed to identify four
Sclerotinia
species:
S. sclerotiorum
(Lib.) de Bary,
S. minor
Jagger,
S. trifoliorum
Erikss., and the undescribed species
Sclerotinia
species 1. DNAs of samples are hybridized with each of five 15-bp oligonucleotide probes containing an SNP site midsequence unique to each species. For additional verification, hybridizations were performed using diagnostic single nucleotide substitutions at a 17-bp sequence of the calmodulin locus. The accuracy of these procedures was compared to that of a restriction fragment length polymorphism (RFLP) method based on Southern hybridizations of EcoRI-digested genomic DNA probed with the ribosomal DNA-containing plasmid probe pMF2, previously shown to differentiate
S. sclerotiorum
,
S. minor
, and
S. trifoliorum.
The efficiency of the SNP-based assay as a diagnostic test was evaluated in a blind screening of 48
Sclerotinia
isolates from agricultural and wild hosts. One isolate of
Botrytis cinerea
was used as a negative control. The SNP-based assay accurately identified 96% of
Sclerotinia
isolates and could be performed faster than RFLP profiling using pMF2. This method shows promise for accurate, high-throughput species identification.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
17 articles.
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